CLCN7 Antikörper (AA 626-805)

Produktnummer ABIN6138670

Produktdetails anti-CLCN7 Antikörper

Target: CLCN7 (Chloride Channel, Voltage-Sensitive 7 (CLCN7))

Bindungsspezifität: AA 626-805

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CLCN7 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: TAREVMSTPV TCLRRREKVG VIVDVLSDTA SNHNGFPVVE HADDTQPARL QGLILRSQLI VLLKHKVFVE RSNLGLVQRR LRLKDFRDAY PRFPPIQSIH VSQDERECTM DLSEFMNPSP YTVPQEASLP RVFKLFRALG LRHLVVVDNR NQVVGLVTRK DLARYRLGKR GLEELSLAQT

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 626-805 of human CLCN7 (NP_001278.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu CLCN7

Target: CLCN7 (Chloride Channel, Voltage-Sensitive 7 (CLCN7))

Andere Bezeichnung: CLCN7 (CLCN7 Produkte)

Synonyme: CLC-7 antikoerper, CLC7 antikoerper, OPTA2 antikoerper, OPTB4 antikoerper, PPP1R63 antikoerper, AA409691 antikoerper, AW538136 antikoerper, ClC-7 antikoerper, D17Wsu51e antikoerper, MGC80627 antikoerper, im:7155923 antikoerper, zgc:153490 antikoerper, CLCN7 antikoerper, chloride voltage-gated channel 7 antikoerper, chloride channel, voltage-sensitive 7 antikoerper, chloride channel, voltage-sensitive 7 L homeolog antikoerper, chloride channel 7 antikoerper, chloride channel protein 7 antikoerper, CLCN7 antikoerper, Clcn7 antikoerper, clcn7.L antikoerper, clcn7 antikoerper, CpipJ_CPIJ008618 antikoerper

Hintergrund: 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.,CLCN7,CLC-7,CLC7,OPTA2,OPTB4,PPP1R63,Cancer,Signal Transduction,Endocrine & Metabolism,CLCN7

Molekulargewicht: 86 kDa/88 kDa

Gen-ID: 1186

UniProt: P51798