DOK7 anticorps
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- Antigène Voir toutes DOK7 Anticorps
- DOK7 (Docking Protein 7 (DOK7))
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Reactivité
- Humain
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Hôte
- Souris
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Clonalité
- Monoclonal
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Conjugué
- Cet anticorp DOK7 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)
- Attributs du produit
- Homo sapiens docking protein 7 (DOK7), transcript variant 1
- Purification
- Purified from mouse ascites fluids by affinity chromatography
- Immunogène
- Full length human recombinant protein of human DOK7(NP_775931) produced in HEK293T cell.
- Clone
- 1D11
- Isotype
- IgG2a
- Top Product
- Discover our top product DOK7 Anticorps primaire
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- Indications d'application
- WB 1:2000, IHC 1:150, FLOW 1:100,
- Commentaires
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The concentration of the product may vary between diferrent lots.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5-1.0 mg/mL
- Buffer
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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
- -20 °C
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- 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
- 52.9 kDa
- ID gène
- 285489
- NCBI Accession
- NM_173660
- HGNC
- 285489
- Pathways
- Skeletal Muscle Fiber Development
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