gibco培养基（我公司不再供应此产品）
gibco培养基（我公司不再供应此产品）
点击：&&时间： 13:20:43&&[ & ]
gibco细胞培养产品
Invitrogen（英杰生命技术）公司旗下著名品牌&&GIBCO的DMEM细胞培养基广泛应用于各种细胞体外培养。
(GIBCO产品目前大部分已直销，我公司仅为终端老客
户代购，经销商等请直接与Invitrogen公司联系。）
抗生素系列
庆大霉素（10mg/ml）
Gentamicin
推荐浓度：0.5-50ug/ml
保存15-30&
庆大霉素（50mg/ml）
Gentamicin
推荐浓度：0.5-50ug/ml
保存15-30&
青霉素-链霉素
Penicillin -Steptomycin
每毫升合剂含5000U青霉素和5000U链霉素，保存：-5 - -20&
青霉素-链霉素
Penicillin -Steptomycin
每毫升合剂含10000U青霉素和10000U链霉素，保存：-5 - -20&
青霉素-链霉素-谷氨酰胺(100X)
Penicillin-Streptomycin-Glutamine
含10000U青霉素，10000ug链霉素和29.2mg谷氨酰胺，保存：-5 - -20&
青霉素-链霉素-新霉素（100X）
PSN antibiotic mixture
每毫升合剂含5mg青霉素、5mg链霉素和10mg新霉素，保存：-5 - -20&
解离产品系列
胰酶，Trpsin，0.25%
不含钙镁离子，含酚红
保存：-5 - -20&
胰酶，Trpsin，2.5%（10X）
无菌条件下以Hank&s液10倍稀释，
不含钙镁离子，保存：-5 - -20&
胰酶-EDTA，
0.05%胰酶，EDTA。4Na
不含钙镁离子，含酚红
保存：-5 - -20&
胰酶-EDTA，（10X）
0. 5%胰酶，EDTA。4Na
无菌条件下以Hank&s液10倍稀释，
不含钙镁离子，保存：-5 - -20&
胰酶-EDTA，
0.25%胰酶，EDTA。4Na
不含钙镁离子，含酚红
保存：-5 - -20&
胰酶（1：250），干粉
保存：2-8&
平衡盐系列
DPBS，（1X）（IVD）
含钙镁离子，不含酚红
DPBS，（1X），（IVD）
含1000mg/l葡萄糖，36mg/l丙酮酸钠，
钙镁离子，不含酚红
DPBS，（10X），（IVD）
含钙镁离子，不含酚红
PBS，（1X）
PBS，（10X）
PBS，（1X）
PBS，（10X）
Gibco 培养基
RPMI 1640，（1X），液体（IVD）
含L-谷氨酰胺
RPMI 1640，（1X），液体（IVD）
含25mM HEPES，和L-谷氨酰胺
RPMI 1640，干粉
含L-谷氨酰胺，不含碳酸氢钠
RPMI 1640，干粉
含L-谷氨酰胺，25mM HEPES，不含碳酸氢钠
RPMI 1640，（1X），液体 &&（ IVD）
不含L-谷氨酰胺
DMEM（低糖），液体
含1000mg/l葡萄糖，L-谷氨酰胺，
110mg/l丙酮酸钠
DMEM（低糖），干粉
含1000mg/l葡萄糖，L-谷氨酰胺，
110mg/l丙酮酸钠，不含碳酸氢钠
DMEM（高糖），液体
含4500ml/l葡萄糖，L-谷氨酰胺
不含丙酮酸钠
DMEM（高糖），液体
含4500ml/l葡萄糖，L-谷氨酰胺110mg/l丙酮酸钠
DMEM（高糖），液体
含4500mg/l葡萄糖，L-谷氨酰胺
25mM HEPES，不含丙酮酸钠
DMEM（高糖），干粉
含4500mg/l葡萄糖，L-谷氨酰胺
不含丙酮酸钠及碳酸氢钠
DMEM（高糖），干粉
含4500mg/l葡萄糖，L-谷氨酰胺
110mg/l丙酮酸钠，不含碳酸氢钠
&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&& GIBCO血清
优级胎牛血清&
最受欢迎的FBS产品。高品质，高价值，适于各种一般的应用&
ES级别胎牛血清
经过ES细胞的培养测试，让您培养ES细胞时无需再预实验试批号
新生牛血清
采集自出生20天内的新生牛
供体动物的EIA检测呈阴性
热灭活马血清
供体动物的EIA检测呈阴性56&下加热30分钟进行热灭活&
采集自供体动物&
&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&&& 杭州四季青血清
无噬菌体、低内毒素特级胎牛血清：本品采自出生前胎牛，3次0．1um过滤。无噬菌体。内毒素含量极低(&5EU/m1)，超过国际先进水平。极佳的促细胞生长繁殖效果。
细胞生长(快)曲线峰值1.6x106
细胞倍增时间(短) 16小时
细胞克隆率(高)&85％
100ml/玻璃瓶
细胞株的保藏及娇贵细胞株(如昆虫细胞、淋巴细胞)的培养
无噬菌体、低内毒素优级胎牛血清：本品采自出生前胎牛，3次0.1um过滤。无噬菌体。内毒素含量极低(&5EU/m1)，超过国际先进水平。极佳的促细胞生长繁殖效果。
细胞生长(快)曲线峰值1.4x106
细胞倍增时间(短)&17小时
细胞克隆率(高)&80％
100ml/玻璃瓶
细胞株的保藏及组织器官培养、单抗研制。
新生牛血清
无噬菌体、低内毒素超级新生牛血清：本品采自出生后2小时内的新生牛，低1gG，3次0.1um过滤。内毒素含量极低(&5EU/m1)，超过国际先进水平。促细胞生长繁殖的三大指标超过国家标准。
细胞生长(快)曲线峰值1.2x106
细胞倍增时间(短)&19小时细胞克隆率(高)&70％
200ml/玻璃瓶
400ml/玻璃瓶
单抗研制、原代和传代细胞培养
无噬菌体、低内毒素特级新生牛血清：本品采自出生后14小时内的新生牛，3次0.1um过滤。各项质量指标均符合2005年版《中国药典》中对牛血清有关要求。具有较好的促细胞生长繁殖效果。
200ml/玻璃瓶 400ml/玻璃瓶
400ml/塑料瓶 500ml/塑料瓶
多种利用原代和传代细胞规模化培养的疫苗生产。
成年牛血清
本品采自健康成年牛，2次0.22um过滤
200ml/玻璃瓶
诊断试剂及标准品生产用。
无支原体山羊血清
本品采自健康山羊，3次0.1um过滤
200ml/玻璃瓶
科研或诊断试剂生产用。
无支原体系列牛血清
无支原体特级胎牛血清： 本品采自出生前胎牛，3次0.1um过滤。极佳的促细胞生长繁殖效果。
细胞生长(快)曲线峰值1.6x106
细胞倍增时间(短)&16小时
细胞克隆率(高)&85％
200ml/玻璃瓶
适合： 娇贵细胞株(如昆虫细胞、淋巴细胞)的培养。
无支原体优级胎牛血清： 本品采自出生前胎牛，3次0.1um过滤。极佳的促细胞生长繁殖效果。
细胞生长(快)曲线峰值1.4x106
细胞倍增时间(短)&7小时
细胞克隆率(高)&80％
200ml/玻璃瓶
适合：组织器官培养、单抗研制。
友情链接：
Copyright 2012 无锡赛维科技有限公司 苏ICP备号
街道地址：闸北区高平路777号永新国际广场618室 传真：021- 电话：021- Email： 邮 编： 200000生物在线声明：以上所展示的信息由企业自行提供，内容的真实性、准确性和合法性由发布企业负责。生物在线对此不承担任何保证责任。
供应商联系卡
上海联硕生物科技有限公司
上海市嘉松中路3555号A1栋
(服务热线：400-)
总机转807分机
所在区域：
产品详细描述
常备现货！低价促销！来电咨询！
供应invitrogen（Gibco）品牌产品，常备现货有：Gibco&1640培养基、Gibco&DMEM高糖培养基、Gibco低糖培养基、Gibco&MEM培养基、Gibco&M199培养基、Gibco&F12培养基、Gibco&D-MEM/F-12培养基、Gibco&IMDM培养基、Gibco&巴西胎牛血清、Gibco乌拉圭胎牛血清、Gibco澳洲胎牛血清、Gibco超低IgG胎牛血清、Gibco热灭活胎牛血清、Gibco干细胞胎牛血清等各类胎牛血清、Gibco细胞培养添加剂&B27和N2、Gibco细胞转染试剂脂质体2000、Gibco胶原酶、Gibco特殊细胞培养液、TRIZOLRNA&提取试剂TRIZOL&REAGENT。
产品名称：Gibco&DMEM干粉培养基（高糖，含丙***酸钠）货号：
品牌：invitrogen（Gibco）
规格：10*1L（即一盒10小袋，每袋可配1L）
市场价格：522元
优惠价：请致电询价
含：&4500&mg/L&D-葡萄糖、L-谷氨酰胺和&110&mg/L&丙***酸钠
不含：碳酸氢钠
保存温度：2-8℃
有效期：3年（36个月）
相关&Gibco&DMEM干粉培养基（高糖，含丙***酸钠）货号：&Gibco培养基有：
&　高糖DMEM，含HEPES，不含丙***酸钠&&500mL&询价&
&　高糖DMEM，不含HEPES，不含丙***酸钠&&500mL&询价&
&　无糖DMEM，不含丙***酸钠&&500mL&询价&
&　高糖DMEM，含丙***酸钠&&500mL&询价&
&　高糖DMEM，不含丙***酸钠&&10&1L&询价&
&　高糖DMEM，含丙***酸钠&&10&1L&询价&
&　高糖DMEM，含丙***酸钠&&1&10L&询价&
&　低糖DMEM&&10&1L&询价&
&　低糖DMEM&&1&10L&询价&
&　MEM&Earles，不含非必需氨基酸&&500mL&询价&
&　MEM&Earles，不含非必需氨基酸&&10&1L&询价&
&　MEM，含非必需氨基酸&&10&1L&询价&
&　IMDM，含碳酸氢钠&&1000mL&询价&
&　IMDM，不含碳酸氢钠&&10&1L&询价&
&　DMEM/F-12，含HEPES&500mL&询价&
&　DMEM/F-12，含HEPES&10&1L&询价&
&　DMEM/F-12，不含HEPES&10&1L&询价&
&　F-12&Nutrient&Mixture&10&1L&询价&
&　Sf-900&II&SFM&1000mL&询价&
&　Advanced&DMEM&500mL&询价&
&　RPMI&mL&询价&
&　RPMI&1640，含HEPES&500mL&询价&
&　RPMI&L&询价&
&　RPMI&1640，含HEPES&10&1L&询价&
&　Advanced&RPMI&mL&询价&
生物在线声明：以上所展示的信息由企业自行提供，内容的真实性、准确性和合法性由发布企业负责。生物在线对此不承担任何保证责任。
查看 Gibco&DMEM干粉培养基（高糖，含丙酮... 产品的用户还对以下产品感兴趣
&&&&[供应商：北京索莱宝科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
&&&&[供应商：上海联硕生物科技有限公司]
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请填写所需产品描述Gibco DMEM
Gibco& DMEM delivers superior quality, consistency and control for your mammalian cell culture.Choose your modified DMEM media from the links below.
The complete
is available.Gibco& DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids and vitamins with F-12's wide variety of components.Product UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM/F-12 is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system (2.438 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Using Advanced DMEMAdvanced DMEM is unique from other media due to the addition of the following ingredients to allow for serum reduction: ethanolamine, glutathione, ascorbic acid, insulin, transferrin, AlbuMAX& I lipid-rich bovine serum albumin for cell culture, and the trace elements sodium selenite, ammonium metavanadate, cupric sulfate, and manganous chloride. Advanced DMEM requires supplementation with 1&5%
and 4 mM L-glutamine or
supplement. Many cell lines do not require adaptation to this media. The FBS concentration must be optimized for each cell line to obtain maximum serum reduction. Advanced DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemFor supply chain continuity, we manufacture Advanced DMEM at two separate facilities located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentrations of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. This DMEM was further modified without lysine and arginine.Product Intended UseFor Research Use Only: Not for use in diagnostic procedures.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). SILAC& protein labeling experiments should be conducted using . DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer a comparable DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. Gibco& DMEM with & supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.Product UseFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical Gibco& DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM with & supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM product made in our Scotland facility (). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.
The complete
is available.Using DMEM/F-12DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids, and vitamins with F-12's wide variety of components. DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemDMEM/F-12 is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM/F-12 product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Gibco& DMEM / F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids and vitamins with F-12's wide variety of components.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM / F-12 is manufactured at a cGMP compliant facility, located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer a comparable Gibco& DMEM / F-12 product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.DMEM / F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM / F-12 may require supplementation, commonly with 10%
(FBS). DMEM / F-12 uses a sodium bicarbonate buffer system and therefore requires a 5-10% CO2 environment to maintain physiological pH.Powder forms of Gibco& cell culture medium require sodium bicarbonate supplementation, pH adjustment, and filtration at the time of preparation (see
for details).
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.Gibco& DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids, and vitamins with F-12's wide variety of components. Gibco& DMEM/F-12 with & supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM/F-12 is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM/F-12 product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system (2.438 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product UseFor Research Use Only: Not intended for animal or human diagnostic or therapeutic use.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from Life Technologies to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured in a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, Life Technologies offers an identical DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM with
supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM product made in our Scotland facility (). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.
The complete
is available.Gibco& DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids and vitamins with F-12's wide variety of components.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM/F-12 is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM/F-12 product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system (2.438 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product UseFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical Gibco& DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
同时，我们也提供完整的。使用 DMEM/F-12DMEM/F-12 是DMEM 和 Ham's F-12的 1:1 混合物。 该配方将 DMEM 的高浓度葡萄糖、氨基酸及维生素与 F-12' 的广泛组分结合在一起。DMEM/F-12 不含蛋白质、脂质或生长因子。因此，DMEM/F-12 培养基需要补充营养成分，通常需要添加 10%
(FBS)。DMEM/F-12 培养基采用碳酸氢钠缓冲体系，因此需要 5&10% CO2 环境来维持生理 pH。cGMP 生产质量体系DMEM/F-12 在位于纽约格陵兰岛、符合 cGMP 要求的工厂内生产。该工厂是在 FDA 登记的医疗仪器生产商，且符合 ISO 13485 标准。为确保供应链条的稳定，我们同时提供由我们的苏格兰工厂生产的等同 DMEM/F-12 产品 ()。后者亦是在 FDA 登记的医疗仪器生产商，且符合 ISO 13485 标准。
The complete
is available.Using DMEM/F-12DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids, and vitamins with F-12's wide variety of components. DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemFor supply chain continuity, we manufacture DMEM/F-12 at two separate facilities, located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from Life Technologies to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, Life Technologies offers an identical DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM with & supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM product made in our Scotland facility (). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.
The complete
is available.Using DMEM/F-12DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids and vitamins with F-12's wide variety of components. DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemFor supply chain continuity, we manufacture DMEM/F-12 at two separate facilities, located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP-manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
DMEM is unique from other media as it contains 4 times the concentrations of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. SILAC DMEM Flex has been further modified to not contain lysine, arginine, and glutamine. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). SILAC protein labeling experiments should be conducted using Gibco& . DMEM uses a sodium bicarbonate buffer system (3.7 g/L), so requires a 5-10% CO2 environment to maintain physiological pH.cGMP Manufacturing and Quality SystemSILAC DMEM Flex is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.
The complete
is available.Using DMEM/F-12DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids, and vitamins with F-12's wide variety of components. DMEM/F-12 with
supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemDMEM/F-12 is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM/F-12 product made in our Scotland facility (). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.
The complete
is available.Using Advanced DMEM/F-12Advanced DMEM/F-12 is unique from other media due to addition of the following ingredients to allow for serum reduction: ethanolamine, glutathione, ascorbic acid, insulin, transferrin, AlbuMAX& II lipid-rich bovine serum albumin for cell culture, and the trace elements sodium selenite, ammonium metavanadate, cupric sulfate, and manganous chloride. Advanced DMEM/F-12 requires supplementation with 1&5%
and 4 mM L-glutamine or
supplement. Many cell lines do not require adaptation to this media. The FBS concentration must be optimized for each cell line to obtain maximum serum reduction. Advanced Advanced DMEM/F-12 uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemFor supply chain continuity, we manufacture Advanced DMEM/F-12 at two separate facilities located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product UseFor Research Use Only: Not intended for animal or human diagnostic or therapeutic use.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer a comparable Gibco& DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.Powder forms of Gibco& cell culture medium require sodium bicarbonate supplementation, pH adjustment, and filtration at the time of preparation (see
for details).
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g / L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers a comparable Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g / L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product UseFor Research Use Only: Not intended for animal or human diagnostic or therapeutic use.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.cGMP manufacturing and quality systemFor supply chain continuity, we manufacture DMEM at two separate facilities, located in Grand Island, NY and Scotland, UK. Both sites are compliant with cGMP-manufacturing requirements, are certified to ISO 13485, and are registered with the FDA as medical device manufacturers.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g / L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. Gibco& DMEM with & supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g / L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g / L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product Intended UseThis Gibco& DMEM formulation has received Pre-market 510k clearance as a Class II medical device for human ex-vivo tissue and cell culture processing applications from the FDA. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from Life Technologies to reference our Type II
(DMF).cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g / L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g / L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product UseFor Research Use Only: Not intended for animal or human diagnostic or therapeutic use.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers a comparable Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g / L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product UseFor Research Use Only: Not intended for animal or human diagnostic or therapeutic use.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
The complete
is available.Gibco& DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids, and vitamins with F-12's wide variety of components.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM/F-12 is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM/F-12 product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system (2.438 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM with
supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH.Product useFor human ex vivo tissue and cell culture processing applications. CAUTION: When used as a medical device, Federal law restricts this device to sale by or on the order of a physician. Customers using Gibco& DMEM in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II
(DMF).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical DMEM product made in our Scotland facility (). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Using DMEM/F-12DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids, and vitamins with F-12's wide variety of components. DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system and therefore requires a 5&10% CO2 environment to maintain physiological pH. Powder forms of Gibco& cell culture media require sodium bicarbonate supplementation, pH adjustment, and filtration at the time of preparation (see
for details).cGMP manufacturing and quality systemDMEM/F-12 is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer a comparable DMEM/F-12 product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Gibco& DMEM/F-12 is a 1:1 mixture of DMEM and Ham's F-12. This formulation combines DMEM's high concentrations of glucose, amino acids and vitamins with F-12's wide variety of components.Product UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM/F-12 is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers a comparable Gibco& DMEM/F-12 product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM/F-12 contains no proteins, lipids, or growth factors. Therefore, DMEM/F-12 may require supplementation, commonly with 10%
(FBS). DMEM/F-12 uses a sodium bicarbonate buffer system (2.438 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5&10% CO2 environment to maintain physiological pH. Powder forms of Gibco& cell culture media require sodium bicarbonate supplementation, pH adjustment, and filtration at the time of preparation (see
for details).cGMP manufacturing and quality systemDMEM is manufactured at a cGMP-compliant facility located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer a comparable DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g / L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. Gibco& DMEM with & supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.Product Intended UseFor in vitro diagnostic use. CAUTION: Not for human or animal therapeutic use. Uses other than the intended use may be a violation of local law.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Paisley, Scotland, UK. The facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard. For supply chain continuity, Life Technologies offers an identical Gibco& DMEM product made in our Grand Island facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 and ISO 9001 standards.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g / L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.在中国境内, 本产品仅限于非临床科研用途, 产品信息以中文为准。 (In China territory, the product is for Research Use only in non-clinical unit, product information in Chinese shall prevail.)
The complete
is available.DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate.Product UseFor Research Use Only: Not intended for animal or human diagnostic or therapeutic use.cGMP Manufacturing and Quality SystemGibco& DMEM is manufactured at a cGMP compliant facility, located in Grand Island, New York. The facility is registered with the FDA as a medical device manufacturer and is certified to ISO 13485 standards. For supply chain continuity, we offer an identical Gibco& DMEM product made in our Scotland facility (). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10%
(FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
The complete
is available.Using DMEMDMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original