CABT-B9981

antibody from Creative Diagnostics
Targeting: CLCN7 CLC-7, CLC7, OPTA2, PPP1R63
Provider product page for CABT-B9981
Western blot
ELISA

Antibody data

Product number
CABT-B9981 - Provider product page
Provider
Creative Diagnostics
Product name
Mouse anti-Human CLCN7 monoclonal antibody, clone 5B4
Antibody type
Monoclonal
Description
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]
Reactivity
Human
Host
Mouse
Conjugate
Unconjugated
Isotype
IgG
Antibody clone number
5B4
Vial size
50 _g
Storage
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
CLCN7 protein structure - CABT-B9981 shown in red.