El medio de lavado de hepatocitos es un medio E de Williams enriquecido para ofrecer una menor filtración de laMás información
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Número de catálogo
Cantidad
17704024
500 mL
Número de catálogo 17704024
Precio (MXN)
-
Cantidad:
500 mL
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El medio de lavado de hepatocitos es un medio E de Williams enriquecido para ofrecer una menor filtración de la membrana celular, facilidad de centrifugación y alta viabilidad.
Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.
Especificaciones
Tipo de productoMedio de lavado de hepatocitos
Cantidad500 mL
Condiciones de envíoTemperatura ambiente
FormularioLíquido
Unit SizeEach
Contenido y almacenamiento
Almacenar en el refrigerador (2–8 °C) y proteger de la luz.
Preguntas frecuentes
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.
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.
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.
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.
My cells are not adhering to the culture vessel. What should I do?
This can occur if cells are overly trypsinized. Trypsinize for a shorter time or use less trypsin. Mycoplasma contamination could also cause this problem. Segregate your culture and test for mycoplasma infection. Lastly, check for attachment factors in the medium.