DOK7 Antikörper (N-Term)

Produktnummer ABIN657491

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.

Klon: RB32528

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody 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: DOK7 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

Haltbarkeit: 6 months

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: 53097

Gen-ID: 285489

NCBI Accession: NP_001158145, NP_001243825, NP_775931

UniProt: Q18PE1

Pathways: Skeletal Muscle Fiber Development