Connexin-26 Polyclonal Antibody, 50ul[BT-AP07988] Plasma Polymorphisms in this gene may

Polymorphisms in this gene may also influence the severity of deafness caused by mitochondrial 12S ribosomal RNA mutations

Alternatively spliced transcript variants encoding multiple isoforms have been observed for PIAS2

disease:Defects in MT-ATP6 are a cause of infantile bilateral striatal necrosis

Members of the MDR/TAP subfamily are involved in multidrug resistance

forms a ternary complex with the protein kinase MAP3K7/TAK1 and either TRAF2 or TRAF6 in response to stimulation with the pro-inflammatory cytokines TNF or IL-1

Connexin-26 Polyclonal Antibody, 50ul[BT-AP07988] Plasma Polymorphisms in this gene mayThis gene encodes a member of the gap junction protein family. The gap junctions were first characterized by electron microscopy as regionally specialized structures on plasma membranes of contacting adherent cells. These structures were shown to consist of cell to cell channels that facilitate the transfer of ions and small molecules between cells. The gap junction proteins, also known as connexins, purified from fractions of enriched gap junctions