Hepatocyte Wash Medium is an enriched Williams' Medium E for the reduction of cell membrane leakage, ease of centrifugation andRead more
Have Questions?
Catalog number 17704024
Price (USD)
120.00
Each
Add to cart
Customize this product
Price (USD)
120.00
Each
Add to cart
Hepatocyte Wash Medium is an enriched Williams' Medium E for the reduction of cell membrane leakage, ease of centrifugation and high viability.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
FormLiquid
Product TypeHepatocyte Wash Medium
Green FeaturesSustainable packaging
Quantity500 mL
Shipping ConditionRoom Temperature
Unit SizeEach
Contents & Storage
Store in refrigerator (2–8°C) and protect from light.
Frequently asked questions (FAQs)
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.