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Earle’s Balanced Salts (Modified) (EBS) (1X Solution) without phenol red
Earle’s Balanced Salts without Sodium Bicarbonate.
The FastCellular senescence detection kit provides:
Higher sensitivity due to a new fluorogenic detection probe
Applicable for living cells and fixed tissues
Ability to quantify SA-?-gal in cellular senescence assay
Short staining time (30 min)
The FastMitophagy Detection Kit is specifically designed for mitophagy detection in mammalian cells.
Hams F10 medium is a nutrient mixture designed to cultivate a wide variety of mammalian and hybridoma cells.
Hams F10 medium is a nutrient mixture designed to cultivate a wide variety of mammalian and hybridoma cells.
Ham’s F-12 medium was designed for low density, serum-free growth of Chinese Hamster Ovary (CHO) cells. Ham’s F-12 is well suited for the growth of primary rat hepatocytes and prostate epithelial cells. It is also the medium of choice for toxicity assays using CHO cells.
Ham’s F-12 medium was designed for low density, serum-free growth of Chinese Hamster Ovary (CHO) cells. Ham’s F-12 is well suited for the growth of primary rat hepatocytes and prostate epithelial cells. It is also the medium of choice for toxicity assays using CHO cells.
Hank’s Balanced Salts (HBS) (Modified) (1X Solution) without calcium, magnesium, phenol red
Hanks’ Balanced Salts solution is used to maintain the pH and osmotic balance in the medium and to provide the cells with water and essential inorganic ions.
Ready to use solution
Cell culture grade
Cell culture grade HEPES (powder). Buffer strength for cell culture applications is usually in the range of 10 to 25 mM. Studies have indicated that 20 mM HEPES is the most satisfactory concentration of the buffer when both Hanks’ and Earle’s solutions are used.
High Growth Enhancement Medium, without L-Glutamine is a modification of DMEM in which 3.6 g/liter fructose is substituted for glucose, resulting in better pH control and higher cell yields. Fructose is metabolized slower than glucose, resulting in slower acid buildup.
High Growth Enhancement Medium is a modification of DMEM in which 3.6 g/liter fructose is substituted for glucose, resulting in better pH control and higher cell yields. Fructose is metabolized slower than glucose, resulting in slower acid buildup.
This media is selective for growth of cells with a functioning HGPRT mechanism. The main application is for the selective growth of hybridoma cells for monoclonal antibody production. (50X, 13.61 mg/L hypoxanthine, 3.876 mg/L thymidine)
IMDM Powder, with L-glutamine, without sodium bicarbonate, BSA, pure human transferrin, and soybean lecithin
IMDM Powder, with L-glutamine, without sodium bicarbonate, BSA, pure human transferrin, and soybean lecithin
ITS Premix stimulates cell proliferation while decreasing substantially the serum requirements for culture of many cell types. Contains 0.5 mg/ml insulin from bovine pancreas, 0.5 mg/ml human transferrin (substantially iron-free) and 0.5 µg/ml sodium selenite. Prepared in Earle’s balanced Salt Solution (EBSS) without phenol red. Sterile-filtered.
L-glutamine is an essential amino acid that is a crucial component of culture media that serves as a major energy source for cells in culture.
In this medium dextrose is replaced by galactose. In addition, buffering is provided by the free bases of the amino acids in place of sodium bicarbonate. As a result this medium has been used for growth of tissues in free gaseous exchange with the atmosphere.