IL-8 mouse Monoclonal Antibody(13F8), 100ul Drying & Desiccation |disease:Defects in KLKB1 are the

|disease:Defects in KLKB1 are the cause of prekallikrein deficiency (PKK deficiency)

Reduced expression of GDF9 may be associated with polycystic ovary syndrome and mutations in this gene may be more common in mothers of dizygotic twins

by the interaction of a vesicle-associated membrane protein termed synaptobrevin/VAMP with a target compartment membrane protein termed syntaxin

RHOG encodes a member of the Rho family of small GTPases

spleen and lymph node

IL-8 mouse Monoclonal Antibody(13F8), 100ul Drying & Desiccation |disease:Defects in KLKB1 are theThe protein encoded by this gene is a member of the CXC chemokine family. This chemokine is one of the major mediators of the inflammatory response. This chemokine is secreted by several cell types. It functions as a chemoattractant, and is also a potent angiogenic factor. This gene is believed to play a role in the pathogenesis of bronchiolitis, a common respiratory tract disease caused by viral infection. This gene and other ten members of the CXC