Aquaporin 4 Monoclonal Antibody(4H1), 100ul Miscellaneous Mutations at highly conserved amino

Mutations at highly conserved amino acid residues in this gene have caused some forms of Charcot-Marie-Tooth (CMT) type 2 neuropathies

This receptor also binds to chemokine (C-X-C motif) ligand 1 (CXCL1/MGSA)

including one with a novel exon that is generated by RNA editing

There are five family members in mammals: relA

disease:A chromosomal aberration involving BCL6 may be a cause of a form of B-cell leukemia

Aquaporin 4 Monoclonal Antibody(4H1), 100ul Miscellaneous Mutations at highly conserved aminoThis gene encodes a member of the aquaporin family of intrinsic membrane proteins that function as water selective channels in the plasma membranes of many cells. This protein is the predominant aquaporin found in brain and has an important role in brain water homeostasis. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. A recent study provided evidence for translational readthrough in this gene