兔抗CLCN7多克隆抗体

Background:

The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood.

Applications:

ELISA, WB

Name of antibody:

CLCN7

Immunogen:

Fusion protein of human CLCN7

Full name:

chloride voltage-gated channel 7

Synonyms:

CLC7; CLC-7; OPTA2; OPTB4; PPP1R63

SwissProt:

P51798

ELISA Recommended dilution:

5000-10000

WB Predicted band size:

89 kDa

WB Positive control:

LoVo and A549 cell, Mouse liver tissue and Rat liver tissue lysates

WB Recommended dilution:

200-1000