CLCN7 antibody

GeneTex

CLCN7 antibody

9

WB: 1:500 - 1:1000. ICC/IF: 1:100 - 1:500. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.

ImmunoFluorescence, Western Blot, ImmunoCytoChemistry

Research Use Only

Polyclonal

Unconjugated

CLCN7

chloride voltage-gated channel 7

chloride channel 7 alpha subunit; chloride channel protein 7; chloride channel, voltage-sensitive 7; CLC7; CLC-7; H(+)/Cl(-) exchange transporter 7; HOD; OPTA2; OPTB4; PPP1R63; protein phosphatase 1, regulatory subunit 63

Rabbit

IgG

H(+)/Cl(-) exchange transporter 7

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. [provided by RefSeq, Jul 2008]

Human, Mouse, Rat

-20°C or -80°C,2°C to 8°C

12352203