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HAX1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

This Recombinant HAX1 protein is produced in HEK-293 Cells.
Catalog No. ABIN2722446

Quick Overview for HAX1 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag) (ABIN2722446)

Target

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

Protein Type

Recombinant

Origin

  • 5
  • 1
Human

Source

  • 4
  • 1
  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 80 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant 1

    Purification tag / Conjugate

    This HAX1 protein is labelled with Myc-DYKDDDDK Tag.

    Characteristics

    • Recombinant human HAX1 (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

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

    Alternative Name

    Hax1

    Background

    The protein encoded by this gene is known to associate with hematopoietic cell-specific Lyn substrate 1, a substrate of Src family tyrosine kinases. It also interacts with the product of the polycystic kidney disease 2 gene, mutations in which are associated with autosomal-dominant polycystic kidney disease, and with the F-actin-binding protein, cortactin. It was earlier thought that this gene product is mainly localized in the mitochondria, however, recent studies indicate it to be localized in the cell body. Mutations in this gene result in autosomal recessive severe congenital neutropenia, also known as Kostmann disease. Two transcript variants encoding different isoforms have been found for this gene.

    Molecular Weight

    31.4 kDa

    NCBI Accession

    NP_006109

    Pathways

    Regulation of Actin Filament Polymerization
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