DOK7 anticorps (N-Term)

N° du produit ABIN657491

Détail du produit anti-DOK7 anticorps

Antigène: DOK7 (Docking Protein 7 (DOK7))

Épitope: AA 26-55, N-Term

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DOK7 est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: 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.

Clone: RB32528

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

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

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Date de péremption: 6 months

Détails sur DOK7

Antigène: DOK7 (Docking Protein 7 (DOK7))

Autre désignation: DOK7 (DOK7 Produits)

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

Sujet: 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.

Poids moléculaire: 53097

ID gène: 285489

NCBI Accession: NP_001158145, NP_001243825, NP_775931

UniProt: Q18PE1

Pathways: Skeletal Muscle Fiber Development