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Gibco™ KnockOut™ DMEM/F-12

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

详情介绍

Gibco™ KnockOut™ DMEM/F-12

Product Type：KnockOut DMEM/F-12.

Manufacturing Quality：cGMP for medical devices, 21 CFR Part 820 and ISO 13485.

Serum Supplementation：KnockOut™.

Shipping Condition：Room Temperature.

Volume (Metric)：500 ml.

Product Line：Gibco™.

Form：Liquid.

Glutamine：No Glutamine.

Phenol Red Indicator：Phenol Red.

Green Features：Sustainable packaging.

Cell Type：Stem Cells (Embryonic), Stem Cells (iPS – Induced Pluripotent Stem).

HEPES Buffer：No HEPES.

Gibco™ DMEM/F-12, powder

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

详情介绍

Gibco™ DMEM/F-12, powder：

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.


Using DMEM/F-12：

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.


Powder forms of Gibco™ cell culture medium require sodium bicarbonate supplementation, pH adjustment, and filtration at the time of preparation (see protocol for details).


cGMP Manufacturing and Quality System：

Gibco™ 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 (32500-035). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.


Gibco™ DMEM/F-12, HEPES

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

详情介绍

Gibco™ DMEM/F-12, HEPES

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 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 (31330-038). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.

Gibco™ Ham’s F-12K (Kaighn’s) Medium

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上海金畔生物科技有限公司提供Gibco™ Ham’s F-12K (Kaighn’s) Medium ，欢迎访问官网了解更多产品信息和订购。
Gibco™ Ham’s F-12K (Kaighn’s) Medium

详情介绍

Gibco™ Ham's F-12K (Kaighn's) Medium

Using Ham's F-12K：

Ham's F-12K (Kaighn's) Medium contains many components not found in traditional basal media, such as putrescine, thymidine, hypoxanthine, zinc, and higher levels of all amino acids and sodium pyruvate. These additions allow the medium to be supplemented with very low levels of serum or defined components, for some cell types. Ham's F-12K (Kaighn's) Medium contains no proteins or growth factors, and is therefore often supplemented with growth factors and Fetal Bovine Serum (FBS). The FBS concentration must be optimized for each cell line. Ham's F-12K (Kaighn's) Medium uses a sodium bicarbonate buffer system (2.5 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.


Dual-site cGMP manufacturing:

For supply chain continuity, we manufacture Ham's F-12K (Kaighn's) Medium 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.

Gibco™ BenchStable™ DMEM/F12

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上海金畔生物科技有限公司提供Gibco™ BenchStable™ DMEM/F12 ，欢迎访问官网了解更多产品信息和订购。
Gibco™ BenchStable™ DMEM/F12

详情介绍

Gibco™ BenchStable™ DMEM/F12 has been engineered for storage at room temperature while supporting cellular proliferation and maximum cell densities comparable to conventional DMEM/F12 when supplemented with ≥10% fetal bovine serum (FBS).                          

Using BenchStable 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 uses a sodium bicarbonate buffer system and therefore requires a 5–10% CO2 environment to maintain physiological pH. DMEM/F-12 with GlutaMAX supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. BenchStable DMEM/F-12 contains no proteins, lipids, or growth factors and so requires supplementation with ≥10% fetal bovine serum (FBS).


cGMP manufacturing and quality system：

Gibco BenchStable media 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.


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™ RPMI 1640 Medium, powder

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上海金畔生物科技有限公司提供Gibco™ RPMI 1640 Medium, powder ，欢迎访问官网了解更多产品信息和订购。
Gibco™ RPMI 1640 Medium, powder

详情介绍

Gibco™ RPMI 1640 Medium, powder

Using RPMI：

RPMI 1640 Medium is unique from other media because it contains the reducing agent glutathione and high concentrations of vitamins. RPMI 1640 Medium contains biotin, vitamin B12, and PABA, which are not found in Eagle's Minimal Essential Medium or Dulbecco's Modified Eagle Medium. In addition, the vitamins inositol and choline are present in very high concentrations. RPMI 1640 Medium contains no proteins, lipids, or growth factors; therefore, requiring supplementation, commonly with 10% Fetal Bovine Serum (FBS). RPMI 1640 Medium uses a sodium bicarbonate buffer system (2.0 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 protocol for details).


cGMP manufacturing and quality system：

RPMI 1640 Medium 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 RPMI 1640 product made in our Scotland facility (51800-019). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.

Gibco™ RPMI 1640 Medium, no glutamine

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上海金畔生物科技有限公司提供Gibco™ RPMI 1640 Medium, no glutamine ，欢迎访问官网了解更多产品信息和订购。
Gibco™ RPMI 1640 Medium, no glutamine

详情介绍

Gibco™ RPMI 1640 Medium, no glutamine

Using RPMI：

RPMI 1640 Medium is unique from other media because it contains the reducing agent glutathione and high concentrations of vitamins. RPMI 1640 Medium contains biotin, vitamin B12, and PABA, which are not found in Eagle's Minimal Essential Medium or Dulbecco's Modified Eagle Medium. In addition, the vitamins inositol and choline are present in very high concentrations. RPMI 1640 Medium contains no proteins, lipids, or growth factors. Therefore, RPMI 1640 Medium requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). RPMI 1640 Medium uses a sodium bicarbonate buffer system (2.0 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.


cGMP manufacturing and quality system：

RPMI 1640 Medium 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 RPMI 1640 product made in our Scotland facility (31870-074). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.


Gibco™ MEM α, no nucleosides

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

详情介绍

Gibco™ MEM α, 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. 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 (22561-054). This facility is registered with the FDA as a medical device manufacturer and is 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™ Opti-MEM™|Reduced Serum Medium

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上海金畔生物科技有限公司提供Gibco™ Opti-MEM™|Reduced Serum Medium ，欢迎访问官网了解更多产品信息和订购。
Gibco™ Opti-MEM™|Reduced Serum Medium

详情介绍

Gibco™ Opti-MEM™|Reduced Serum Medium

Using Opti-MEM™ I Medium：

Opti-MEM™ I Reduced-Serum Medium is a unique medium that contains insulin, transferrin, hypoxanthine, thymidine, and trace elements. These additional components allow for a reduction in serum supplementation by at least 50%. Opti-MEM™ I medium uses a sodium bicarbonate buffer system (2.4 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.


cGMP manufacturing and quality system：

Opti-MEM™ I 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 Opti-MEM™ I product made in our Scotland facility (31985-047). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.

Gibco™ DMEM, high glucose, pyruvate, no glutamine

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上海金畔生物科技有限公司提供Gibco™ DMEM, high glucose, pyruvate, no glutamine ，欢迎访问官网了解更多产品信息和订购。
Gibco™ DMEM, high glucose, pyruvate, no glutamine

详情介绍

Gibco™ DMEM, high glucose, pyruvate, no glutamine

Using DMEM：

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. 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：

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 DMEM product made in our Scotland facility (21969-035). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.


Gibco™ Medium 199, no phenol red

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上海金畔生物科技有限公司提供Gibco™ Medium 199, no phenol red ，欢迎访问官网了解更多产品信息和订购。
Gibco™ Medium 199, no phenol red

详情介绍

Gibco™ Medium 199, no phenol red

Compared to other basal media, Medium 199 contains unique components, including adenine, adenosine, hypoxanthine, thymine, and additional vitamins. Medium 199 is available with Earle's salts for use in a CO2 incubator, or with Hanks' salts for use without CO2.


Product Use：

For Research Use Only: Not intended for animal or human diagnostic or therapeutic use.


cGMP Manufacturing and Quality System：

Gibco™ Medium 199 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.


Medium 199 contains no proteins, lipids, or growth factors. Medium 199 uses a sodium bicarbonate buffer system (2.2 g/L) and therefore requires a 5–10% CO2 environment to maintain physiological pH.


Gibco™ DMEM, high glucose, GlutaMAX™ Supplement, H

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

详情介绍

Gibco™ DMEM, high glucose, GlutaMAX™ Supplement, HEPES

Using DMEM：

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. DMEM with GlutaMAX™ 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% 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：

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 DMEM product made in our Scotland facility (32430-100). This facility is also registered with the FDA as a medical device manufacturer and certified to the ISO 13485 standard.

Gibco™ Medium 199

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上海金畔生物科技有限公司提供Gibco™ Medium 199 ，欢迎访问官网了解更多产品信息和订购。
Gibco™ Medium 199

详情介绍

Gibco™ Medium 199

Compared to other basal media, Medium 199 contains unique components, including adenine, adenosine, hypoxanthine, thymine, and additional vitamins. Medium 199 is available with Earle's salts for use in a CO2 incubator, or with Hanks' salts for use without CO2.


cGMP Manufacturing and Quality System：

Gibco™ Medium 199 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™ Medium 199 product made in our Scotland facility (31150-022). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.


Medium 199 contains no proteins, lipids, or growth factors. Medium 199 uses a sodium bicarbonate buffer system (2.2 g/L) and therefore requires a 5–10% CO2 environment to maintain physiological pH.

Gibco™ Brinster’s, no Glutamine, no phenol red

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上海金畔生物科技有限公司提供Gibco™ Brinster’s, no Glutamine, no phenol red ，欢迎访问官网了解更多产品信息和订购。
Gibco™ Brinster’s, no Glutamine, no phenol red

详情介绍

Gibco™ Brinster's, no Glutamine, no phenol red

Gibco™ Brinster's medium is unique from other media as it contains no amino acids or vitamins. Brinster's medium is supplemented with bovine serum albumin required for supporting oocyte maturation and the early stages of mammalian embryo development and pyruvate as an essential energy source.


Product Use:

For Research Use Only: Not intended for animal or human diagnostic or therapeutic use.


cGMP Manufacturing:

Gibco™ Brinster's medium 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.


Brinster's medium uses a sodium bicarbonate buffer system (2.1 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.

Gibco™ MEM, no glutamine

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

详情介绍

Gibco™ MEM, no glutamine

Gibco™ MEM, developed by Harry Eagle, was based on his earlier formulation of Basal Medium Eagle (BME). Many other modifications of MEM followed, including Glasgow’s MEM, MEM α, DMEM, and Temin’s Modification. MEM is available with Earle’s salts for use in a CO2 incubator, or with Hanks' salts for use without CO2. This product is made with Earle’s salts.


Using MEM：

MEM contains no proteins, lipids, or growth factors. Therefore, MEM requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). MEM 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 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 product made in our Scotland facility (21090-055). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standard.


Gibco™ DMEM, high glucose, GlutaMAX™ Supplement, p

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

详情介绍

Gibco™ DMEM, high glucose, GlutaMAX™ Supplement, pyruvate

Using DMEM：

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. DMEM with GlutaMAX™ 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% 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：

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 DMEM product made in our Scotland facility (31966-021). 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.