RPMI 1640 Medium, ohne Phenolrot
RPMI 1640 Medium, ohne Phenolrot
RPMI 1640 Medium, ohne Phenolrot
RPMI 1640 Medium, ohne Phenolrot
Gibco™

RPMI 1640 Medium, ohne Phenolrot

RPMI 1640 Medium wurde ursprünglich zur Züchtung leukämischer Humanzellen in Suspension und als Monolayer entwickelt. Roswell Park Memorial Institute (RPMI)Weitere Informationen
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KatalognummerMenge
11835030500 mL
Katalognummer 11835030
Preis (EUR)
47,46
Each
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Menge:
500 mL
Customize this product
Preis (EUR)
47,46
Each
Zum Warenkorb hinzufügen
RPMI 1640 Medium wurde ursprünglich zur Züchtung leukämischer Humanzellen in Suspension und als Monolayer entwickelt. Roswell Park Memorial Institute (RPMI) 1640 Medium wurde seitdem für eine Reihe von Säugetierzellen wie HeLa, Jurkat, MCF-7, PC12, PBMC, Astrozyten und Karzinome als geeignet befunden. Wir bieten verschiedene RPMI 1640 Medium-Modifikationen für eine Vielzahl von Zellkulturanwendungen an. Finden Sie die richtige Zusammensetzung mithilfe des Medien-Auswahlwerkzeuges.

Dieses RPMI wurde wie folgt modifiziert:
mitOhne
• L-Glutamin• HEPES
• Phenolrot

Die vollständige Zusammensetzung ist verfügbar.

Verwendung von RPMI
RPMI 1640 Medium unterscheidet sich deutlich von anderen Medien, da es das Reduktionsmittel Glutathion sowie hohe Konzentrationen an Vitaminen enthält. RPMI 1640 Medium enthält Biotin, Vitamin B12 und PABA, welche nicht in Eagle's Minimal Essential Medium bzw. Dulbecco's Modified Eagle Medium enthalten sind. Darüber hinaus sind die Vitamine Inositol und Cholin in sehr hohen Konzentrationen enthalten. RPMI 1640 Medium enthält keine Proteine, Lipide oder Wachstumsfaktoren. Aus diesem Grund erfordert RPMI 1640 Medium eine Supplementierung, gewöhnlich mit 10 % fetalem Rinderserum (FBS). RPMI 1640 Medium verwendet ein Natriumbikarbonat-Puffersystem (2,0 g/l) und erfordert daher eine CO2-Umgebung von 5 bis 10 %, um den physiologischen pH-Wert aufrechtzuerhalten.

cGMP-konformes Herstellungs- und Qualitätssystem
RPMI 1640 Medium wird in einer cGMP-konformen Einrichtung in Grand Island, New York, hergestellt. Die Produktion(sanlage) ist von der US-Arzneimittelbehörde FDA als Hersteller medizinischer Geräte zugelassen und ISO 13485-zertifiziert. Zur Gewährleistung einer ununterbrochenen Versorgungskette bieten wir ein identisches RPMI 1640-Produkt aus unserem Betrieb in Schottland an (11835-063). Diese Einrichtung ist von der US-Arzneimittelbehörde FDA als Hersteller von Medizinprodukten zugelassen und ISO 13485-zertifiziert.
Für die Verwendung in der Forschung oder die Weiterverarbeitung. Nicht zur Diagnosestellung oder direkten Anwendung bei Menschen oder Tieren geeignet.
Specifications
ZelllinieHeLa, Jurkat, MCF-7, PC-12, PBMC, Astrozyten und Karzinome
ZelltypLeukämische Zellen
Konzentration1 X
Fertigungsqualität, HerstellungsqualitätcGMP-compliant under the ISO 13485 standard
ProduktlinieGibco
ProdukttypRPMI 1640 Medium (Roswell Park Memorial Institute 1640 Medium)
Menge500 mL
Haltbarkeit12 Monate ab Herstellungsdatum
VersandbedingungRaumtemperatur
KlassifikationOhne Stoffe tierischen Ursprungs
FormFlüssig
Serum LevelStandard-Serumzugabe
SterilitätSteril gefiltert
Sterilization MethodSterile-filtered
Mit AdditivenGlutamin
Ohne AdditiveKeine HEPES, Kein Phenolrot, Ohne Natriumpyruvat
Unit SizeEach
Inhalt und Lagerung
Lagerbedingungen: 2 °C bis 8 °C (vor Licht schützen)
Versandbedingungen: Haltbarkeit bei
Raumtemperatur: 12 Monate ab Herstellungsdatum

Häufig gestellte Fragen (FAQ)

How light sensitive is RPMI 1640 media? Should I also be protecting it from LED light?

While we know that different wavelengths of light are worse than others for exposure, we would recommend as a best practice to protect the medium from all forms of light exposure including LEDs, as much as possible to ensure optimal performance, as several components within the medium are light sensitive, such as vitamins.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

What is the density (g/L) for RPMI 1640 Medium?

We have specific gravity information for RPMI 1640 Medium: 1.006 kg/L. In this case, the specific gravity is the same as density as the solvent is water.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

Do you offer RPMI 1640 medium without both methionine and phenol red?

We offer RPMI 1640 Medium, no methionine (Cat. No. A1451701) and also offer RPMI Medium, no phenol red (Cat. Nos. 11835030, 11835055, 11835063, and 11835105). However, we do not offer RPMI 1640 medium without both methionine and phenol red as a standard catalog product. Our Customs group can make it for you as a custom media. If you are interested, please complete this Custom order inquiry form PDF (https://www.thermofisher.com/content/dam/LifeTech/global/applied-sciences/pdfs/Bioproduction/Gibco-Custom-Media-Buffers-Request-Form.pdf) and email it to custommedia@thermofisher.com. Our Customs group will review your requirements and get back to you within a couple of days with pricing, ordering information, and lead time. After that, you have the choice of proceeding with an “official” order or declining.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

I understand that some media are worse than others for fluorescence imaging. How do I choose?

Most media contain phenol red, which can quench fluorescent dyes in the visible wavelengths. Most media also contain autofluorescent components, such as riboflavin, which can reduce signal-to-background. We offer FluoroBrite DMEM and HEPES-based Live Cell Imaging Solution, which have been optimized for fluorescent imaging. We also offer a number of media without phenol red. But if none of these are reasonable options for your experiment, then we also offer BackDrop Background Suppressor ReadyProbes Reagent, which can be added to quench media autofluorescence.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Should I be concerned about phenol red in my media when labeling my live cells with fluorescent dyes?

Some cell types accumulate phenol red, and this can pose a problem in the use of many fluorescent probes. Phenol red can quench visible-wavelength dyes and, although phenol red is non-fluorescent, various impurities may be fluorescent. We have many phenol red-free media to choose from. Our Live Cell Imaging Solution (HEPES-based) and our FluoroBrite DMEM have been optimized to be phenol red-free as well as to be non-autofluorescent.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Zitierungen und Referenzen (3)

Zitierungen und Referenzen
Abstract
Inhibition of both paracrine and autocrine VEGF/ VEGFR-2 signaling pathways is essential to induce long-term remission of xenotransplanted human leukemias.
Authors: Dias S; Hattori K; Heissig B; Zhu Z; Wu Y; Witte L; Hicklin D J; Tateno M; Bohlen P; Moore M A; Rafii S;
Journal:Proc Natl Acad Sci U S A
PubMed ID:11553814
'Antiangiogenic agents block the effects of tumor-derived angiogenic factors (paracrine factors), such as vascular endothelial growth factor (VEGF), on endothelial cells (EC), inhibiting the growth of solid tumors. However, whether inhibition of angiogenesis also may play a role in liquid tumors is not well established. We recently have shown that ... More
Regulation of neural differentiation by normal and mutant (G654A, amyloidogenic) gelsolin.
Authors: Westberg J A; Zhang K Z; Andersson L C;
Journal:FASEB J
PubMed ID:10463954
'Gelsolin belongs to a family of proteins that modulate the structural dynamics of cytoskeletal actin. Gelsolin activity is required for the redistribution of actin occurring during membrane ruffling, cell crawling, and platelet activation. A point mutation (G654A) in the gelsolin gene causes a dominantly inherited systemic amyloidosis called familial amyloidosis ... More
Inhibition of mitochondrial respiration by endogenous nitric oxide: a critical step in Fas signaling.
Authors: Beltrán Belén; Quintero Marisol; García-Zaragozá Eugenia; O'Connor Enrique; Esplugues Juan V; Moncada Salvador;
Journal:Proc Natl Acad Sci U S A
PubMed ID:12077295
We have found that activation of human adult T cell leukemia (Jurkat) cells with anti-Fas Ab leads, in a concentration-dependent manner, to an early burst of production of nitric oxide (NO), which inhibits cell respiration. This results in mitochondrial hyperpolarization, dependent on the hydrolysis of glycolytic ATP by the F1F(o)-ATPase ... More