CLCN7 rabbit polyclonal antibo

gene_symbol：CLCN7
predicted_size：89 kDa
Uniprot ID：P51798
description：CLCN7 rabbit polyclonal antibody
clonality：Polyclonal
product_type(primary antibody, secondy antibody ,tag antibody,Loding Control...)：Primary Antibodies
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.
immunogen：Fusion protein of human CLCN7
recommended_dilution：WB: 500-2000 WB positive control: HepG2, A549, LOVO cell lysates IHC: 100-300 Positive control: Human esophagus cancer Predicted cell location: Cytoplasm
predicted_size：89 kDa
buffer：pH7.4 PBS, 0.05% NaN3, 40% Glycerol
host_species：Rabbit
applications：IHC, WB
reactivities：Human, Mouse, Rat