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Gibco™ RPMI 1640 Medium

RPMI 1640 Medium

8.29 € - 205.00 €

Specifications

Certifications/Compliance ISO 13485 standards, FDA
Form Liquid
Product Type RPMI 1640 Medium
For Use With (Application) Mammalian cell culture
Regulatory Status For in-vitro diagnostic use
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Products 6
Product Code Brand With Additives Without Additives Quantity Price Quantity & Availability  
Product Code Brand With Additives Without Additives Quantity Price Quantity & Availability  
11530586
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Gibco™
21875034
Glutamine, Phenol Red No HEPES, No Sodium Pyruvate 500 mL
20.05 €
500mL
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11540586
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Gibco™
21875042
Glutamine, Phenol Red No HEPES, No Sodium Pyruvate 100 mL
8.29 €
100mL
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10432512
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Gibco™
21875059
Glutamine, Phenol Red No HEPES, No Sodium Pyruvate 1000 mL
38.01 €
1 L
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11560586
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Gibco™
21875109
Glutamine, Phenol Red No HEPES, No Sodium Pyruvate 20 x 100 mL
146.00 €
1 set
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10247302
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Gibco™
21875158
Glutamine, Phenol Red No HEPES, No Sodium Pyruvate 6 x 1000 mL
205.00 €
Pack of 6
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11554446
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Gibco™
31870082
Phenol Red No Glutamine, No HEPES, No Sodium Pyruvate 20 x 100 mL
147.00 €
Pack of 20
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Description

Description

Roswell Park Memorial Institute (RPMI) 1640 medium was originally developed to culture human leukemic cells in suspension and as a monolayer. RPMI 1640 has since been found suitable for a variety of mammalian cells including HeLa, Jurkat, MCF-7, PC12, PBMC, astrocytes, and carcinomas. We offer a variety of Gibco™ RPMI 1640 modifications for a range of cell culture applications.



Gibco™ RPMI 1640 is unique from other media because it contains the reducing agent glutathione and high concentrations of vitamins. RPMI 1640 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.

Product Intended Use
For 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. Customers using Gibco™ RPMI 1640 in a manufacturing process, who have a submission with the FDA, may request a letter of authorization from us to reference our Type II Drug Master File (DMF).

cGMP Manufacturing and Quality System
Gibco™ RPMI 1640 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™ RPMI 1640 product made in our Grand Island facility (11875-127). This facility is registered with the FDA as a medical device manufacturer and is certified to the ISO 13485 standards.

RPMI 1640 contains no proteins, lipids, or growth factors. Therefore, RPMI 1640 requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). RPMI 1640 uses a sodium bicarbonate buffer system (2.0 g/L) and therefore requires a 5-10% CO2 environment to maintain physiological pH.
Specifications

Specifications

ISO 13485 standards, FDA
RPMI 1640 Medium
For in-vitro diagnostic use
Liquid
Mammalian cell culture
Videos
SDS
Documents

Documents

Product Certifications