CLCN1 Antikörper

Produktnummer ABIN6570089

Produktdetails anti-CLCN1 Antikörper

Target: CLCN1 (Chloride Channel 1, Skeletal Muscle (CLCN1))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser CLCN1 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: Affinity purification

Immunogen: Recombinant protein of human CLCN1

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1 mg/mL

Buffer: 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 CLCN1

Target: CLCN1 (Chloride Channel 1, Skeletal Muscle (CLCN1))

Andere Bezeichnung: CLCN1 (CLCN1 Produkte)

Synonyme: CLCN1 antikoerper, si:dkey-14o18.5 antikoerper, Clc-1 antikoerper, Clc1 antikoerper, SMCC1 antikoerper, adr antikoerper, mto antikoerper, myotonia antikoerper, nmf355 antikoerper, SMCC antikoerper, CLC1 antikoerper, chloride voltage-gated channel 1 antikoerper, chloride channel, voltage-sensitive 1a antikoerper, chloride channel protein 1 antikoerper, chloride channel, voltage-sensitive 1 antikoerper, CLCN1 antikoerper, clcn1a antikoerper, LOC100550479 antikoerper, LOC703944 antikoerper, Clcn1 antikoerper

Hintergrund:

Synonyms: Chloride channel protein 1,Chloride channel protein,Chloride channel protein skeletal muscle,CIC 1,CIC1,ClC-1,CLC1,Clcn1,CLCN1,MGC138361,MGC142055,skeletal muscle

Background: The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. The protein encoded by this gene regulates the electric excitability of the skeletal muscle membrane. Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). Alternative splicing results in multiple transcript variants.

Molekulargewicht:

Observed_MW: 115kDa

Calculated_MW: 108kDa

Gen-ID: 1180

UniProt: P35523