MAGB3 Polyclonal Antibody, 50ul Pathway and Network Analysis Mutations in this gene cause

Mutations in this gene cause distal renal tubular acidosis associated with sensorineural deafness

with high sensitivity and precision

and it can rescue bacterial resistance to alkylhydroperoxide in E

VitroGel MSC is ready-to-use with an optimized formulation that fully supports the rapid expansion of MSCs

May be involved in regulation of endocytosis and intracellular trafficking of G-protein-coupled receptors (GPCRs)

MAGB3 Polyclonal Antibody, 50ul Pathway and Network Analysis Mutations in this gene causeThis gene is a MAGE B subfamily member of the MAGE gene family. MAGE family member proteins direct the expression of tumor antigens recognized on a human melanoma by autologous cytolytic T lymphocytes. There are two known clusters of MAGE genes on chromosome X. The members of the MAGE A subfamily are located in the Xq28 region, while the members of the MAGE B subfamily are clustered in the Xp21 region.