IMDM, ohne Phenolrot
Gibco™

IMDM, ohne Phenolrot

Iscove's Modified Dulbecco's Medium (IMDM) eignet sich gut für schnell proliferierende Zellkulturen hoher Dichte, einschließlich Jurkat, COS-7, und Makrophagen. WirWeitere Informationen
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KatalognummerMenge
21056023500 mL
Katalognummer 21056023
Preis (EUR)
28,20
Each
Menge:
500 mL
Customize this product
Preis (EUR)
28,20
Each
Iscove's Modified Dulbecco's Medium (IMDM) eignet sich gut für schnell proliferierende Zellkulturen hoher Dichte, einschließlich Jurkat, COS-7, und Makrophagen. Wir bieten viele Gibco™ IMDM-Modifikationen für eine Vielzahl von Zellkulturanwendungen. Finden Sie die richtige Zusammensetzung mithilfe des Medien-Auswahlwerkzeuges.
Dieses IMDM wurde wie folgt modifiziert:
Mit Ohne
• L-Glutamin • Phenolrot
• α-thioglycerol
• 2-Mercaptoethanol


Die vollständige Zusammensetzung ist verfügbar.

IMDM, eine Modifikation von Dulbecco's Modified Eagle Medium, enthält Selen sowie zusätzliche Aminosäuren und Vitamine. Außerdem fehlt diesem einzigartigen Medium Eisen, wobei Kaliumnitrat das Eisennitrat ersetzt.

Produktverwendung
Nur für Forschungszwecke: Nicht für die Diagnostik oder Therapie von Tieren oder Menschen bestimmt.

CGMP-Herstellungs- und Qualitätssystem
Gibco™ IMDM wird in einer cGMP-konformen Einrichtung in Grand Island, New York, hergestellt. Die Einrichtung ist bei der FDA als Hersteller von Medizinprodukten registriert und nach ISO 13485 zertifiziert.

IMDM enthält keine Proteine, Lipide oder Wachstumsfaktoren. Aus diesem Grund kann bei IMDM eine Supplementierung, meist mit 10 % fötalem Rinderserum (FBS), erforderlich sein. IMDM nutzt ein Puffersystem mit Natriumbikarbonat (3,024 g/l) und erfordert daher eine 5 bis 10%ige CO2-Umgebung zur Aufrechterhaltung des physiologischen pH-Werts.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
ZelllinieJurkat, COS-7 und Makrophagen
Konzentration1 X
Fertigungsqualität, HerstellungsqualitätcGMP-compliant under the ISO 13485 standard
ProduktlinieGibco
ProdukttypIMDM (Iscove's Modified Dulbecco's Medium)
Menge500 mL
Haltbarkeit12 Monate ab Herstellungsdatum
VersandbedingungRaumtemperatur
KlassifikationOhne Stoffe tierischen Ursprungs
FormFlüssig
SterilitätSteril gefiltert
Mit AdditivenHoher Glukosegehalt, Glutamin, HEPES, Natriumpyruvat
Ohne AdditiveKein Phenolrot, Kein α-Thioglycerol, Kein 2-Mercaptoethanol
Unit SizeEach
Inhalt und Lagerung
Lagerbedingungen: 2 bis 8 °C, vor Licht schützen
Versandbedingungen: Haltbarkeit bei
Raumtemperatur: 12 Monate ab Herstellungsdatum

Häufig gestellte Fragen (FAQ)

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.

How long can I keep my media after supplementing with serum?

Generally speaking, media can be used for up to three weeks after supplementation with serum. There are no formal studies to support this, but it is the rule of thumb used by our scientists.

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

My medium was shipped at room temperature but it is supposed to be stored refrigerated. Is it okay?

We routinely ship media that require long-term storage in the refrigerator at room temperature. We have done studies on representative media formulations to show that media can be at room temperature for up to a week without a problem.

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

How can I remove mycoplasma contamination from my cell culture medium?

Very often mycoplasma contamination cannot be removed from the culture so it should be discarded. You may have a unique culture that you prefer not to discard and would like to try to clean it. Ciprofloxacin and Plasmocin have reportedly been used for this application. If interested in a protocol or directions for use, check with the antibiotic supplier or published literature. Note that mycoplasma are very difficult to remove from culture and spread easily so the treated cultures should be quarantined until clear of mycoplasma, and your laboratory should be thoroughly cleaned.

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

Zitierungen und Referenzen (3)

Zitierungen und Referenzen
Abstract
Nongenomic testosterone calcium signaling. Genotropic actions in androgen receptor-free macrophages.
Authors:Guo Z, Benten WP, Krucken J, Wunderlich F
Journal:J Biol Chem
PubMed ID:12048191
'Steroid hormones exert genotropic actions through members of the nuclear receptor family. Here, we have demonstrated genotropic actions of testosterone that are independent of intracellular androgen receptors (iAR). Through plasma membrane androgen receptors (mAR), testosterone induces a rapid rise in the intracellular free Ca(2+) concentration of iAR-free murine RAW 264.7 ... More
The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3.
Authors:Fredericks WJ, Galili N, Mukhopadhyay S, Rovera G, Bennicelli J, Barr FG, Rauscher FJ 3rd
Journal:Mol Cell Biol
PubMed ID:7862145
Alveolar rhabdomyosarcomas are pediatric solid tumors with a hallmark cytogenetic abnormality: translocation of chromosomes 2 and 13 [t(2;13) (q35;q14)]. The genes on each chromosome involved in this translocation have been identified as the transcription factor-encoding genes PAX3 and FKHR. The NH2-terminal paired box and homeodomain DNA-binding domains of PAX3 are ... More
Role of JunB in erythroid differentiation.
Authors: Jacobs-Helber Sarah M; Abutin Randolph M; Tian Cuixia; Bondurant Maurice; Wickrema Amittha; Sawyer Stephen T;
Journal:J Biol Chem
PubMed ID:11726656
The role of junB as a regulator of erythroid cell survival, proliferation, and differentiation was tested by controlled expression of JunB in the erythropoietin (EPO)-dependent erythroleukemia cell line HCD57. JunB induced erythroid differentiation as evidenced by increased expression of the erythroid-specific proteins beta-globin, spectrin-alpha, and TER-119. Expression of JunB for ... More