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Gibco™ RPMI 1640 Medium, GlutaMAX™ Supplement, HEPES
RPMI 1640 Medium, GlutaMAX™ Supplement, HEPES
144.00 SEK - 3500.00 SEK
Specifications
Certifications/Compliance | ISO 13485 standards, FDA |
---|---|
Form | Liquid |
Product Type | Roswell Park Memorial Institute (RPMI) 1640 Medium |
With Additives | GlutaMAX, Phenol Red, HEPES |
Without Additives | No Sodium Pyruvate |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
---|---|---|---|---|---|---|---|---|---|
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
11534526
|
Gibco™
72400013 |
100 mL |
144.00 SEK
100mL |
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11544526
|
Gibco™
72400021 |
500mL |
388.00 SEK
500mL |
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11564526
|
Gibco™
72400112 |
20 x 100mL |
2460.00 SEK
Pack of 20 |
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11554526
|
Gibco™
72400054 |
10 x 500mL |
3500.00 SEK
5000mL |
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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. Find the right formulation using the media selector tool.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. Gibco™ RPMI 1640 with GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format.
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).
Dual-Site cGMP Manufacturing
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 a comparable Gibco™ RPMI 1640 product made in our Grand Island facility (72400-047). 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
ISO 13485 standards, FDA | |
Roswell Park Memorial Institute (RPMI) 1640 Medium | |
No Sodium Pyruvate |
Liquid | |
GlutaMAX, Phenol Red, HEPES | |
Mammalian cell culture |