CLCN7 Polyclonal Antibody | G-AB-11356

CLCN7 Polyclonal Antibody | G-AB-11356 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Metabolism, Signal Transduction

Synonyms: CLCN7, CLC-7, CLC7, OPTA2, OPTB4, PPP1R63

Reactivity: Human, Mouse, Rat

Host: Rabbit

Isotype: IgG

Gene ID: 1186

Accession #:

Clonality:

Immunogen: Recombinant fusion protein of human CLCN7 (NP_001278.1) .

Clone #:

Conjugation: Unconjugated

Swissprot: P51798

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 1 mg/mL

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Purification method: Affinity purification

Application: IHC

Dilution: IHC 1:50-1:200

Storage: Store at -20°C. Avoid freeze / thaw cycles.

CLCN7 Polyclonal Antibody DataSheet