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Merck

R1145

SAFC

RPMI-1640 Medium

Without ʟ-glutamine, folic acid and sodium bicarbonate, sterile liquid, suitable for cell culture, 10x

Synonim(y):

RPMI Medium, RPMI-1640 Culture Medium, Roswell Park Memorial Institute 1640 medium

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About This Item

Numer MDL:
Kod UNSPSC:
12352207
NACRES:
NA.75

product name

RPMI-1640 Medium, 10 ×, Without L-glutamine, folic acid and sodium bicarbonate, liquid, sterile-filtered, suitable for cell culture

sterylność

sterile-filtered

Postać

liquid

stężenie

10 ×

metody

cell culture | mammalian: suitable

zanieczyszczenia

endotoxin, tested

komponenty

NaHCO3: no
phenol red: yes
sodium pyruvate: no
HEPES: no
L-glutamine: no

Warunki transportu

ambient

temp. przechowywania

2-8°C

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Opis ogólny

RPMI 1640 Medium was developed at Roswell Park Memorial Institute in 1966 by Moore and his co-workers. A modification of McCoy′s 5A Medium, it was formulated to support lymphoblastoid cells in suspension culture, but it has since been shown to support a wide variety of cells that are anchorage-dependent. Originally intended to be used with a serum supplement, RPMI 1640 has been shown to support several cell lines in the absence of serum. It has also been widely used in fusion protocols and in the growth of hybrid cells. This medium is suitable for culturing human normal and neoplastic leukocytes.

Rekonstytucja

Supplement with 0.3 g/L L-glutamine, 2.0 g/L sodium bicarbonate, 0.001 g/L folic acid at 1×.

Piktogramy

Exclamation mark

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Eye Irrit. 2

Kod klasy składowania

10 - Combustible liquids

Klasa zagrożenia wodnego (WGK)

WGK 2

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


Certyfikaty analizy (CoA)

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Odwiedź Bibliotekę dokumentów

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Yoichi Matsuo et al.
International journal of cancer, 124(4), 853-861 (2008-11-28)
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Oleh Taratula et al.
Journal of controlled release : official journal of the Controlled Release Society, 140(3), 284-293 (2009-07-02)
Low penetration ability of Small Interfering RNA (siRNA) through the cellular plasma membrane combined with its limited stability in blood, limits the effectiveness of the systemic delivery of siRNA. In order to overcome such difficulties, we constructed a nanocarrier-based delivery

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