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A6886

CLCN7 Rabbit polyclonal antibody

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£152.00

SKU:
A6886
Zusätzliche Namen:
CLC-7|CLC7|CLCN7|HOD|OPTA2|OPTB4|PPP1R63
Anwendung:
ELISA, WB
Molekulargewicht:
110kDa
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Abclonal
Host:
Rabbit
Reaktivitäten:
Human, Mouse, Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulierung:
Unmodified
Sequenz:
TAREVMSTPVTCLRRREKVGVIVDVLSDTASNHNGFPVVEHADDTQPARLQGLILRSQLIVLLKHKVFVERSNLGLVQRRLRLKDFRDAYPRFPPIQSIHVSQDERECTMDLSEFMNPSPYTVPQEASLPRVFKLFRALGLRHLVVVDNRNQVVGLVTRKDLARYRLGKRGLEELSLAQT
Uniprot:
P51798
Synonyme:
chloride channel 7 alpha subunit;chloride channel protein 7;chloride channel, voltage-sensitive 7;CLC-7;CLC7;H(+)/Cl(-) exchange transporter 7;HOD;OPTA2;OPTB4;PPP1R63;protein phosphatase 1, regulatory subunit 63
Weitere Details:
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.
Versandbedingungen:
Blue Ice