L-15 Medium (Leibovitz) is formulated for use in carbon dioxide (CO2) free systems requiring sodium bicarbonate supplements. It supports established cell lines, such as human larynx epidermoid cells (HEp-2) and Rhesus monkey kidney epithelial cells (LLC-MK2), as well as primary explants of embryonic and adult human tissue. L-15 medium can also be used for culturing viruses.
Anwendung
L-15 Medium (Leibovitz) has been used:
to study the toxicity of silver nanoparticles (AgNPs) with primary cultures of Eisenia fetida coelomocytes[1]
to culture crab hepatopancreas and ovary tissues[2]
as a component of the dissociation medium for infusion of the pancreas of mice[3]
Menge
Formulated to contain 13.8 grams of powder per liter of medium.
Insect biochemistry and molecular biology, 27(5), 387-395 (1997-05-01)
Prostaglandins of the 2-series (e.g. PGE2) are typically synthesized from arachidonic acid (AA) after AA is released from cellular phospholipids after activation of an intracellular phospholipase A2 (PLA2). Treatment of isolated salivary glands with PLA2 inhibitor oleyloxyethyl phosphorylcholine (OPC) or
Marek's disease (MD) is an oncogenic, lymphoproliferative, and highly contagious disease of chickens. Its etiologic agent is the alphaherpesvirus Marek's disease virus (MDV, Gallid alphaherpesvirus 2), and it is a chronic and ubiquitous problem for the poultry industry with significant
This is the first demonstration of the study of glycan protein turnover in living cells by FTIR with commercially available tetraacetylated N-Azidoacetyl-D-Mannosamine (Ac4ManNAz) label. The FTIR analysis has shown to be able to monitor the metabolism of glycans in living
Effect of estradiol on vitellogenesis and oocyte development of female swimming crab, Portunus trituberculatus
Ranavirus is the second most common infectious cause of amphibian mortality. These viruses affect caudates, an order in which information regarding Ranavirus pathogenesis is scarce. In the Netherlands, two strains (CMTV-NL I and III) were suspected to possess distinct pathogenicity
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