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

This gene encodes a bipartite protein with distinct amino- and carboxy-terminal domains

Abundant expression is detected only in reconstructed epidermis and is restricted to differentiating keratinocytes

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

SHANK2 encodes a protein that is a member of the Shank family of synaptic proteins that may function as molecular scaffolds in the postsynaptic density of excitatory synapses

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