DMEM, high glucose, GlutaMAX™ Supplement, pyruvate
DMEM, high glucose, GlutaMAX™ Supplement, pyruvate
Gibco™

DMEM, high glucose, GlutaMAX™ Supplement, pyruvate

DMEM (Dulbecco's Modified Eagle Medium) is a widely used basal medium for supporting the growth of many different mammalian cells.Read more
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Catalog NumberQuantity
31966021
also known as 31966-021
500 mL
10569010500 mL
31966047
also known as 31966-047
10 x 500 mL
Catalog number 31966021
also known as 31966-021
Price (EUR)
37,63
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Quantity:
500 mL
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Price (EUR)
37,63
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DMEM (Dulbecco's Modified Eagle Medium) is a widely used basal medium for supporting the growth of many different mammalian cells. Cells successfully cultured in DMEM include primary fibroblasts, neurons, glial cells, HUVECs, and smooth muscle cells, as well as cell lines such as HeLa, 293, Cos-7, and PC-12. We offer a variety of DMEM modifications for a range of cell culture applications. Find the right formulation using the media selector tool.


This DMEM is modified as follows:
WithWithout
• High Glucose• HEPES
• Sodium Pyruvate 
• GlutaMAX™ 
• Phenol Red 


The complete formulation is available.

Using DMEM
DMEM is unique from other media as it contains 4 times the concentration of amino acids and vitamins than the original Eagle's Minimal Essential Medium. DMEM was originally formulated with low glucose (1 g/L) and sodium pyruvate, but is often used with higher glucose levels, with or without sodium pyruvate. DMEM with GlutaMAX™ supplement minimizes toxic ammonia build-up and improves cell viability and growth in an easy-to-use format. DMEM contains no proteins, lipids, or growth factors. Therefore, DMEM requires supplementation, commonly with 10% Fetal Bovine Serum (FBS). DMEM uses a sodium bicarbonate buffer system (3.7 g/L), and therefore requires a 5–10% CO2 environment to maintain physiological pH.

For Research Use or Further Manufacturing. Not for diagnostic use or direct administration into humans or animals.
Specifications
Concentration1 X
Manufacturing QualitycGMP-compliant under the ISO 13485 standard
Product TypeDulbecco's Modified Eagle Medium (DMEM)
Quantity500 mL
Shelf Life12 Months
ClassificationAnimal Origin-free
Culture TypeMammalian Cell Culture
FormLiquid
SterilitySterile-filtered
Sterilization MethodSterile-filtered
With AdditivesHigh Glucose, GlutaMAX, Sodium Pyruvate, Phenol Red
Without AdditivesNo HEPES
Unit SizeEach
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Certificates

Lot #Certificate TypeDateCatalog Number(s)
3166049Certificate of AnalysisJun 06, 202510569069, 10569077, 10569010
3186051Certificate of AnalysisMay 30, 202510569069, 10569077, 10569010
3228070Certificate of AnalysisMay 29, 202510569069, 10569077, 10569010
3124463Certificate of AnalysisMay 29, 202531966021
3135514Certificate of AnalysisApr 26, 202510569069, 10569077, 10569010
5 results displayed, search above for a specific certificate

Safety Data Sheets

Frequently asked questions (FAQs)

Manganese is not present in the formulation of our catalog DMEM media products.

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

Yes. If you suspect that this is the case, remove the medium and add fresh medium. Alternatively, you can supplement medium with growth-promoting components. It is also possible to substitute GlutaMax I or II for glutamine in the medium to prevent glutamine exhaustion.

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

In all media containing GlutaMAX supplement dipeptides as a substitute for L-glutamine, concentration is equimolar with the L-glutamine in the original formulation.

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

Citations & References (5)

Citations & References
Abstract
A comparison between different human hepatocyte models reveals profound differences in net glucose production, lipid composition and metabolism in vitro.
Authors:Bonanini F,Singh M,Yang H,Kurek D,Harms AC,Mardinoglu A,Hankemeier T
Journal:Experimental cell research
PubMed ID:38499143
Membrane topology influences N-glycosylation of the prion protein.
Authors:Walmsley AR, Zeng F, Hooper NM,
Journal:EMBO J
PubMed ID:11179215
'The glycosylation state of the glycosyl-phosphatidylinositol (GPI) anchored cellular prion protein (PrPC) can influence the formation of the disease form of the protein responsible for the neurodegenerative spongiform encephalopathies. We have investigated the role of membrane topology in the N-glycosylation of PrP by expressing a C-terminal transmembrane anchored form, PrP-CTM, ... More
The protein SET binds the neuronal Cdk5 activator p35nck5a and modulates Cdk5/p35nck5a activity.
Authors: Qu Dianbo; Li Qing; Lim Hui-Ying; Cheung Nam Sang; Li Rong; Wang Jerry H; Qi Robert Z;
Journal:J Biol Chem
PubMed ID:11741927
'The neuronal Cdk5 kinase is composed of the catalytic subunit Cdk5 and the activator protein p35(nck5a) or its isoform, p39(nck5ai). To identify novel p35(nck5a)- and p39(nck5ai)-binding proteins, fragments of p35(nck5a) and p39(nck5ai) were utilized in affinity isolation of binding proteins from rat brain homogenates, and the isolated proteins were identified ... More
Production of mice using iPS cells and tetraploid complementation.
Authors:Zhao XY, Lv Z, Li W, Zeng F, Zhou Q,
Journal:Nat Protoc
PubMed ID:20431542
'Induced pluripotent stem cells (iPSCs) are considered to be an attractive alternative to embryonic stem cells (ESCs) and may provide great potential for clinical applications in regenerative medicine. Although possessing characteristics similar to ESCs, the true pluripotency of these newly studied iPSCs was not known because none of the previously ... More
Rapid generation of functional human IgG antibodies derived from Fab-on-phage display libraries.
Authors:Jostock T, Vanhove M, Brepoels E, Van Gool R, Daukandt M, Wehnert A, Van Hegelsom R, Dransfield D, Sexton D, Devlin M, Ley A, Hoogenboom H, Müllberg J,
Journal:J Immunol Methods
PubMed ID:15251413
We introduce a procedure for the rapid generation of fully human antibodies derived from
5 total citations

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