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Gibco™ RPMI 1640 Medium, no phenol red
RPMI 1640 Medium, no phenol red
283.00 SEK - 2430.00 SEK
Specifications
Certifications/Compliance | ISO 13485 standards, FDA |
---|---|
Content And Storage | 2 to 8°C |
Concentration | 1 X |
Form | Liquid |
Product Type | RPMI 1640 Medium |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
---|---|---|---|---|---|---|---|---|---|
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
11530406
|
Gibco™
11835063 |
500 mL |
283.00 SEK
500mL |
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12060356
|
Gibco™
11835105 |
10 x 500 mL |
2430.00 SEK
Pack of 10 |
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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.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).
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 an identical Gibco™ RPMI 1640 product made in our Grand Island facility (11835-055). 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 | |
1 X | |
RPMI 1640 Medium | |
No Phenol Red, No HEPES, No Sodium Pyruvate | |
For research use only |
2 to 8°C | |
Liquid | |
Glutamine | |
Mammalian cell culture |
Safety and Handling
missing translation for 'shelfLife' : 12 Months