DOK7 Antikörper (N-Term)

Produktnummer ABIN5533390

Produktdetails anti-DOK7 Antikörper

Target: DOK7 (Docking Protein 7 (DOK7))

Bindungsspezifität: AA 26-55, N-Term

Reaktivität: Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser DOK7 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This DOK7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 26-55 amino acids from the N-terminal region of human DOK7.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: For WB starting dilution is: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Details zu DOK7

Target: DOK7 (Docking Protein 7 (DOK7))

Andere Bezeichnung: DOK7 (DOK7 Produkte)

Synonyme: si:dkey-180b4.3 antikoerper, si:ch211-164d19.2 antikoerper, C4orf25 antikoerper, CMS1B antikoerper, A930013K19Rik antikoerper, AW049091 antikoerper, Dok-7 antikoerper, EF-12 antikoerper, Oit5 antikoerper, RGD1566416 antikoerper, dok-7 antikoerper, docking protein 7 antikoerper, DOK7 antikoerper, dok7 antikoerper, Dok7 antikoerper

Hintergrund: The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants.

Molekulargewicht: 53 kDa

Gen-ID: 285489

UniProt: Q18PE1

Pathways: Skeletal Muscle Fiber Development