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DTNA antibody

This Mouse Monoclonal antibody specifically detects DTNA in WB, IF and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN2719779

Quick Overview for DTNA antibody (ABIN2719779)

Target

See all DTNA Antibodies
DTNA (Dystrobrevin alpha (DTNA))

Reactivity

  • 17
  • 13
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 16
  • 7
Mouse

Clonality

  • 19
  • 4
Monoclonal

Conjugate

  • 18
  • 1
  • 1
  • 1
  • 1
  • 1
This DTNA antibody is un-conjugated

Application

  • 22
  • 14
  • 9
  • 8
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone

1A2
  • Characteristics

    Homo sapiens dystrobrevin, alpha (DTNA), transcript variant 5

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human DTNA (NP_116761) produced in HEK293T cell.

    Isotype

    IgG2a
  • Application Notes

    WB 1:2000, IF 1:100, FLOW 1:100

    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C
  • Target

    DTNA (Dystrobrevin alpha (DTNA))

    Alternative Name

    DTNA

    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.

    Molecular Weight

    58.7 kDa

    Gene ID

    1837

    NCBI Accession

    NM_032979

    HGNC

    1837
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