标签归档：glutamax

McCoy’s 5A培养基 GlutaMAX™补充剂

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上海金畔生物科技有限公司提供McCoy’s 5A培养基 GlutaMAX™补充剂 ，欢迎访问官网了解更多产品信息和订购。
McCoy’s 5A培养基 GlutaMAX™补充剂

详情介绍

McCoy's 5A培养基 GlutaMAX™补充剂

Dr. Thomas McCoy originally formulated McCoy's 5A medium as a modification of Basal Medium 5A. Unlike other media, McCoy's 5A contains the reducing agent glutathione, bacto-peptone, and a high level of glucose. This product also includes Dr. Hsu's addition of Hanks' salts to enable use outside a CO2 incubator.


cGMP Manufacturing and Quality System:

Gibco™ McCoy's 5A 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.


Gibco™ McCoy's 5A (modified) requires serum supplementation, commonly with 10% Fetal Bovine Serum (FBS). Gibco™ McCoy's 5A (modified) uses a sodium bicarbonate buffer system (2.2 g/L) and therefore requires a 5–10% CO2 environment to maintain physiological pH.

Gibco IMDM培养基, GlutaMAX™ Supplement

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上海金畔生物科技有限公司提供Gibco IMDM培养基, GlutaMAX™ Supplement ，欢迎访问官网了解更多产品信息和订购。
Gibco IMDM培养基, GlutaMAX™ Supplement

详情介绍

Gibco IMDM培养基, GlutaMAX™ Supplement

IMDM, a modification of Dulbecco's Modified Eagle Medium, includes selenium as well as additional amino acids and vitamins. In addition, this unique medium lacks iron, with potassium nitrate replacing ferric nitrate. Gibco™ IMDM with GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.


cGMP Manufacturing and Quality System:

Gibco™ IMDM 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, we offer an identical Gibco™ IMDM product made in our Grand Island facility (31980-097). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standards.


IMDM contains no proteins, lipids, or growth factors. Therefore, IMDM requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). IMDM uses a sodium bicarbonate buffer system (3.024 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.

Ham’s F-12营养混合物, GlutaMAX™ Supplement

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上海金畔生物科技有限公司提供Ham’s F-12营养混合物, GlutaMAX™ Supplement ，欢迎访问官网了解更多产品信息和订购。
Ham’s F-12营养混合物, GlutaMAX™ Supplement

详情介绍

Ham's F-12营养混合物, GlutaMAX™ Supplement

Compared to other basal media, F-12 contains a wider variety of components, including zinc, putrescine, hypoxanthine, and thymidine. Serum-free growth of CHO cells in F-12 has led to a variety of improved formulations. Gibco™ F-12 with GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.


cGMP Manufacturing and Quality System:

Gibco™ 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, we offer an identical Gibco™ F-12 product made in our Grand Island, New York facility (31765-092). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standards.


Gibco™ F-12 contains no proteins or growth factors. Therefore, F-12 requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). F-12 uses a sodium bicarbonate buffer system (1.176 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.

Gibco™ IMDM, GlutaMAX™ Supplement

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上海金畔生物科技有限公司提供Gibco™ IMDM, GlutaMAX™ Supplement ，欢迎访问官网了解更多产品信息和订购。
Gibco™ IMDM, GlutaMAX™ Supplement

详情介绍

Gibco™ IMDM, GlutaMAX™ Supplement

Using IMDM：

IMDM, a modification of Dulbecco's Modified Eagle Medium, includes selenium as well as additional amino acids and vitamins. In addition, this unique medium lacks iron, with potassium nitrate replacing ferric nitrate. IMDM with GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. IMDM contains no proteins, lipids, or growth factors. Therefore, IMDM requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). IMDM uses a sodium bicarbonate buffer system (3.024 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.


cGMP manufacturing and quality system：

IMDM 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 IMDM product made in our Scotland facility (31980-048). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.

Gibco™ MEM α, nucleosides, GlutaMAX™ Supplement

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上海金畔生物科技有限公司提供Gibco™ MEM α, nucleosides, GlutaMAX™ Supplement ，欢迎访问官网了解更多产品信息和订购。
Gibco™ MEM α, nucleosides, GlutaMAX™ Supplement

详情介绍

Gibco™ MEM α, nucleosides, GlutaMAX™ Supplement

Gibco™ MEM α is a modification of Minimum Essential Medium (MEM) that contains non-essential amino acids, sodium pyruvate, lipoic acid, vitamin B12, biotin, and ascorbic acid. MEM α is available without nucleosides for use as a selection medium for DG44 and other DHFR negative cells. Gibco™ MEM α with GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. This product is made with Earle’s salts.


Using MEM:

MEM α contains no proteins, lipids, or growth factors. Therefore, MEM α requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). MEM α uses a sodium bicarbonate buffer system (2.2 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.


cGMP Manufacturing and Quality System:

Gibco™ MEM α 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™ MEM α product made in our Scotland facility (32571-093). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.

Gibco™ MEM α, GlutaMAX™ Supplement, no nucleosides

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上海金畔生物科技有限公司提供Gibco™ MEM α, GlutaMAX™ Supplement, no nucleosides ，欢迎访问官网了解更多产品信息和订购。
Gibco™ MEM α, GlutaMAX™ Supplement, no nucleosides

详情介绍

Gibco™ MEM α, GlutaMAX™ Supplement, no nucleosides

Using MEM α:

MEM α is a modification of Minimum Essential Medium (MEM) that contains non-essential amino acids, sodium pyruvate, lipoic acid, vitamin B12, biotin, and ascorbic acid. MEM α is available without nucleosides for use as a selection medium for DG44- and other DHFR-negative cells. MEM α with GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. This product is made with Earle’s salts. MEM α contains no proteins, lipids, or growth factors. Therefore, MEM α requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). MEM α uses a sodium bicarbonate buffer system (2.2 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.


cGMP manufacturing and quality system:

MEM α 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 MEM α product made in our Scotland facility (32561-094). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.


Gibco DMEM低糖培养基, GlutaMAX™ Supplement

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上海金畔生物科技有限公司提供Gibco DMEM低糖培养基, GlutaMAX™ Supplement ，欢迎访问官网了解更多产品信息和订购。
Gibco DMEM低糖培养基, GlutaMAX™ Supplement

详情介绍

Gibco DMEM低糖培养基, GlutaMAX™ Supplement

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 GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.


Using DMEM：

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.


cGMP Manufacturing and Quality System：

Gibco™ 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 (21885-108). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.


Gibco™ DMEM/F-12, GlutaMAX™ supplement

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上海金畔生物科技有限公司提供Gibco™ DMEM/F-12, GlutaMAX™ supplement ，欢迎访问官网了解更多产品信息和订购。
Gibco™ DMEM/F-12, GlutaMAX™ supplement

详情介绍

Gibco™ DMEM/F-12, GlutaMAX™ supplement

Using DMEM/F-12：

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. DMEM/F-12 with GlutaMAX™ 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% Fetal Bovine Serum (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 system：

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 an identical DMEM/F-12 product made in our Scotland facility (31331-028). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.