DOK7 Antibody (5G8)


Western Blot: DOK7 Antibody (5G8) [NBP2-02079] Analysis of extracts (35ug) from 9 different cell lines by usin g anti-DOK7 monoclonal antibody (HepG2: human; HeLa: human; SVT2: mouse; A549: human; COS7: monkey; Jurkat: more
Immunocytochemistry/ Immunofluorescence: DOK7 Antibody (5G8) [NBP2-02079] - Staining of COS7 cells transiently transfected by pCMV6-ENTRY DOK7.
Immunohistochemistry-Paraffin: DOK7 Antibody (5G8) [NBP2-02079] - Staining of paraffin-embedded Adenocarcinoma of Human ovary tissue using anti-DOK7 mouse monoclonal antibody.
Flow Cytometry: DOK7 Antibody (5G8) [NBP2-02079] - HEK293T cells transfected with either overexpression plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-DOK7 antibody, and then analyzed by more
Western Blot: DOK7 Antibody (5G8) [NBP2-02079] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY DOK7 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 more

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DOK7 Antibody (5G8) Summary

Full length human recombinant protein of human DOK7(NP_775931) produced in HEK293T cell.
Immunogen affinity purified
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  • Western Blot 1:500-2000
  • Flow Cytometry 1:100
  • Immunocytochemistry/Immunofluorescence 1:100
  • Immunohistochemistry 1:10-1:500
  • Immunohistochemistry-Paraffin 1:150

Reactivity Notes


Packaging, Storage & Formulations

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
PBS (pH 7.3), 1.0% BSA and 50% Glycerol
0.02% Sodium Azide
Immunogen affinity purified

Alternate Names for DOK7 Antibody (5G8)

  • C4orf25
  • C4orf25chromosome 4 open reading frame 25
  • CMS1B
  • docking protein 7
  • DOK7
  • Dok-7
  • Downstream of tyrosine kinase 7
  • FLJ33718
  • FLJ39137
  • FLJ90556
  • protein Dok-7


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. [provided by RefSeq].


This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Gene Symbol DOK7