Dystrobrevin alpha Antibody (1A2)

Images

 
Western Blot: Dystrobrevin alpha Antibody (1A2) [NBP2-03439] - HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY Dystrobrevin alpha (Right lane) cDNA for 48 hrs and lysed. Equivalent ...read more
Flow Cytometry: Dystrobrevin alpha Antibody (1A2) [NBP2-03439] - HEK293T cells transfected with either overexpression plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-Dystrobrevin alpha ...read more
Immunofluorescence: Dystrobrevin alpha Antibody (1A2) [NBP2-03439] - Staining of COS7 cells transiently transfected by pCMV6-ENTRY Dystrobrevin alpha.

Product Details

Summary
Product Discontinued
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Order Details


    • Catalog Number
      NBP2-03439
    • Availability
      Product Discontinued

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Dystrobrevin alpha Antibody (1A2) Summary

Immunogen
Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.
Isotype
IgG2a
Clonality
Monoclonal
Host
Mouse
Gene
DTNA
Purity
Immunogen affinity purified
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Applications/Dilutions

Dilutions
  • Western Blot 1:2000
  • Flow Cytometry 1:100
  • Immunocytochemistry/Immunofluorescence 1:100

Reactivity Notes

Human

Packaging, Storage & Formulations

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

Alternate Names for Dystrobrevin alpha Antibody (1A2)

  • Alpha-dystrobrevin
  • D18S892EDTN
  • DRP3FLJ96209
  • DTN-1
  • DTN-2
  • DTN-3
  • DTN-A
  • dystrobrevin alpha
  • dystrobrevin, alpha
  • Dystrophin-related protein 3
  • LVNC1

Background

The protein encoded by this gene belongs to the dystrobrevin subfamily of the dystrophin family. This protein is a component of the dystrophin-associated protein complex (DPC), which consists of dystrophin and several integral and peripheral membrane proteins, including dystroglycans, sarcoglycans, syntrophins and alpha- and beta-dystrobrevin. The DPC localizes to the sarcolemma and its disruption is associated with various forms of muscular dystrophy. Mutations in this gene are associated with left ventricular noncompaction with congenital heart defects. Multiple alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq].

Limitations

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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Bioinformatics

Gene Symbol DTNA
Entrez