Olfactory receptor 52N4 Polyclonal Antibody, 20ul Nucleic Acid Amplification Certain mutations in KLKB1 cause

Certain mutations in KLKB1 cause prekallikrein deficiency

characterized by a decreased ability to metabolize the enzyme's substrates

this kinase is involved in many cellular processes such as proliferation

Mutations in this gene are associated with chronic obstructive pulmonary disease (COPD)

with homology to gp130

Olfactory receptor 52N4 Polyclonal Antibody, 20ul Nucleic Acid Amplification Certain mutations in KLKB1 causeOlfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G protein coupled receptors (GPCR) arising from single coding exon genes. Olfactory receptors share a 7 transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein mediated