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HAX1 antibody (AA 1-279)

The Mouse Monoclonal anti-HAX1 antibody has been validated for WB, ELISA, IF and ICC. It is suitable to detect HAX1 in samples from Human.
Catalog No. ABIN5775949
$411.54
Plus shipping costs $50.00
Shipping to: United States
Delivery in 13 to 16 Business Days

Quick Overview for HAX1 antibody (AA 1-279) (ABIN5775949)

Target

See all HAX1 Antibodies
HAX1 (HCLS1 Associated Protein X-1 (HAX1))

Reactivity

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  • 22
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  • 2
  • 2
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Human

Host

  • 54
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Mouse

Clonality

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  • 7
Monoclonal

Conjugate

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  • 1
  • 1
  • 1
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  • 1
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  • 1
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This HAX1 antibody is un-conjugated

Application

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  • 28
  • 15
  • 13
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  • 4
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  • 1
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Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunocytochemistry (ICC)

Clone

AT3C5
  • Binding Specificity

    • 15
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    • 1
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    AA 1-279

    Purpose

    Human HAX-1 antibody

    Purification

    Purified

    Immunogen

    Recombinant human HAX1 (1-279aa) purified from E. coli

    Isotype

    IgG2b kappa
  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    Phosphate-Buffered Saline ( pH 7.4) with 0.02 % Sodium Azide, 10 % glycerol

    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

    4 °C,-20 °C,-80 °C

    Storage Comment

    Can be stored at +2C to +8C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
  • Target

    HAX1 (HCLS1 Associated Protein X-1 (HAX1))

    Alternative Name

    HAX-1

    Background

    HAX1 is known to associate with hematopoietic cell-specific Lyn substrate 1 (HS1), one of the substrates of receptor-coupled tyrosine kinases activated during clonal expansion and deletion in lymphoid cells. It also interacts with the product of the polycystic kidney disease 2 (PKD2) gene and with the F-actin-binding protein, cortactin. HAX1 is also reported to bind to hairpin structures in vimentin and DNA polymerase beta mRNAs, so may play a role in mRNA stability and transport. It may also function in promoting cell survival. Defects in HAX1 are the cause of autosomal recessive severe congenital neutropenia 3 (SCN3) also called Kostmann disease.

    NCBI Accession

    NP_006109

    Pathways

    Regulation of Actin Filament Polymerization
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