DMEM, alto contenido en glucosa, sin glutamina
DMEM, alto contenido en glucosa, sin glutamina
Citas y referencias (6)
Gibco™

DMEM, alto contenido en glucosa, sin glutamina

El DMEM (medio Eagle modificado de Dulbecco) se utiliza ampliamente como un medio basal para favorecer el crecimiento de diferentesMás información
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Número de catálogoCantidad
119600776 x 1000 mL
11960044500 mL
1196006910 × 500 mL
119600511000 mL
Número de catálogo 11960077
Precio (USD)
391,50
Each
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Cantidad:
6 x 1000 mL
Customize this product
Precio (USD)
391,50
Each
Añadir al carro de la compra
El DMEM (medio Eagle modificado de Dulbecco) se utiliza ampliamente como un medio basal para favorecer el crecimiento de diferentes células de mamífero. Las células cultivadas con éxito en DMEM incluyen fibroblastos primarios, neuronas, células gliales, HUVEC y células de músculo liso, así como líneas de células HeLa, 293, cos-7 y PC-12. Ofrecemos una variedad de modificaciones de DMEM para diversas aplicaciones de cultivos celulares. Busque la formulación adecuada mediante la herramienta de selección de medios.

Este DMEM se ha modificado de la siguiente manera:
ConSin
• Alto contenido en glucosa• L-glutamina
• Rojo de fenol• Piruvato sódico
• Ácido 4-(2-hidroxietil)piperazin-1-iletanosulfónico (HEPES)

Está disponible la formulación completa.

Uso de DMEM
El medio DMEM es único con respecto a otros medios, ya que contiene 4 veces la concentración de aminoácidos y vitaminas del medio esencial mínimo de Eagle. DMEM se formuló originalmente con bajas cantidades de glucosa (1 g/l) y piruvato sódico, pero a menudo se utiliza con niveles de glucosa más altos, y con o sin piruvato sódico. DMEM no contiene proteínas, lípidos ni factores de crecimiento. Por lo tanto, el DMEM requiere suplementación, generalmente con un 10 % de suero fetal bovino (SFB). DMEM utiliza un sistema de tampones de bicarbonato sódico (3,7 g/l) y, por tanto, requiere un ambiente con un 5–10 % de CO2 para mantener el pH fisiológico.

Sistema cGMP de fabricación y calidad
DMEM se fabrica en unas instalaciones que cumplen con las buenas prácticas de fabricación actuales ubicadas en Grand Island, Nueva York (EE. UU.). Las instalaciones están registradas en la Agencia estadounidense de alimentos y medicamentos (FDA) como fabricante de dispositivos médicos y están certificadas según la norma ISO 13485.

Para su uso en investigación o procesos de fabricación posteriores. No apto para uso diagnóstico ni para la administración directa en seres humanos ni en animales.

Especificaciones
Línea de célulasHeLa, 293, Cos-7, and PC-12
Tipo de célulaPrimary Fibroblasts, Neurons, Glial Cells, HUVECs, Smooth Muscle Cells
Concentración1 X
Calidad de fabricacióncGMP-compliant under the ISO 13485 standard
Línea de productosGibco
Tipo de productoDMEM (Dulbecco's Modified Eagle Medium)
Cantidad6 x 1000 mL
Duración de almacenamiento12 Months From Date of Manufacture
Condiciones de envíoTemperatura ambiente
ClasificaciónAnimal Origin-free
FormularioLíquido
Serum LevelSuplementos de suero estándar
EsterilidadEstéril con filtro
Sterilization MethodSterile-filtered
Con aditivosHigh Glucose, Phenol Red
Sin aditivosNo Glutamine, No HEPES, No Sodium Pyruvate
Unit SizeEach
Contenido y almacenamiento
Condiciones de almacenamiento: De 2 °C a 8 °C (proteger de la luz)
Condiciones de envío: Ambiente
Vida útil: 12 meses a partir de la fecha de fabricación

Preguntas frecuentes

What is the manganese concentration in DMEM? Do you offer manganese-free DMEM?

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.

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.

I see a decrease in growth of my culture. What should I do?

Try changing the medium or serum. Compare media formulations for differences in glucose, amino acids, and other components. Compare an old lot of serum with a new lot. Increase initial cell inoculums. Lastly, adapt cells sequentially to new medium.

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

View all DMEM, alto contenido en glucosa, sin glutamina FAQs

Citations & References (6)

Citations & References
Abstract
Fibroblast growth factor receptor-1 signaling induces osteopontin expression and vascular smooth muscle cell-dependent adventitial fibroblast migration in vitro.
Authors: Li Guohong; Oparil Suzanne; Kelpke Stacey S; Chen Yiu-Fai; Thompson John A;
Journal:Circulation
PubMed ID:12176960
'BACKGROUND: Increased expression of osteopontin (OPN), fibroblast growth factors (FGFs), and their type-1 receptor (FGFR-1) is associated with neointima formation and atherosclerosis. This study tested the hypothesis that ligand activation of FGFR-1 stimulates OPN expression in rat aortic smooth muscle cells (RASMCs), explored the signaling pathway involved, and assessed the ... 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
Isolation of mouse mesenchymal stem cells on the basis of expression of Sca-1 and PDGFR-a.
Authors:Houlihan DD, Mabuchi Y, Morikawa S, Niibe K, Araki D, Suzuki S, Okano H, Matsuzaki Y
Journal:Nat Protoc
PubMed ID:23154782
Platelet-derived growth factor receptor a (PDGFR-a) and stem cell antigen 1 (Sca-1) have recently been identified as selective markers of mouse mesenchymal stem cells (MSCs). PDGFR-a(+)Sca-1(+) (PaS) MSCs have augmented growth potential and robust tri-lineage differentiation compared with standard culture-selected MSCs. In addition, the selective isolation of PaS MSCs avoids ... More
Ascorbic-acid transporter Slc23a1 is essential for vitamin C transport into the brain and for perinatal survival.
Authors: Sotiriou Sotiria; Gispert Suzana; Cheng Jun; Wang Yaohui; Chen Amy; Hoogstraten-Miller Shelley; Miller Georgina F; Kwon Oran; Levine Mark; Guttentag Susan H; Nussbaum Robert L;
Journal:Nat Med
PubMed ID:11984580
The only proven requirement for ascorbic acid (vitamin C) is in preventing scurvy, presumably because it is a cofactor for hydroxylases required for post-translational modifications that stabilize collagen. We have created mice deficient in the mouse ortholog (solute carrier family 23 member 1 or Slc23a1) of a rat ascorbic-acid transporter, ... More
Characterization of the 46-kDa intermediates of matrix metalloproteinase 3 (stromelysin 1) obtained by site-directed mutation of phenylalanine 83.
Authors: Benbow U; Butticè G; Nagase H; Kurkinen M;
Journal:J Biol Chem
PubMed ID:8631880
The precursor of matrix metalloproteinase 3 (MMP-3/ stromelysin 1) is activated in vitro by proteinases or mercurial compounds by stepwise processes which include the initial formation of short-lived intermediates and the subsequent intermolecular cleavage of the His82-Phe83 bond to generate the fully activated mature MMP-3 (Nagase, H., Enghild, J. J., ... More
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