Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

HAX1 antibody

This Rabbit Polyclonal antibody specifically detects HAX1 in WB and ELISA. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7114867

Quick Overview for HAX1 antibody (ABIN7114867)

Target

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

Reactivity

  • 61
  • 20
  • 17
  • 4
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 52
  • 8
  • 1
Rabbit

Clonality

  • 54
  • 7
Polyclonal

Conjugate

  • 32
  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This HAX1 antibody is un-conjugated

Application

  • 51
  • 28
  • 15
  • 13
  • 13
  • 7
  • 6
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    HCLS1 associated protein X-1

    Isotype

    IgG
  • Application Notes

    WB: 1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    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

    Storage Comment

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    HAX1

    Background

    Synonyms:FLJ17042, FLJ18492, FLJ93803, HAX 1, HAX1, HCLS1 associated protein X 1, HCLSBP1, HS1 associating protein X 1, HS1 binding protein 1, HS1BP1, HSP1BP 1, SCN3 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 kDa, 36 kDa

    UniProt

    O00165

    Pathways

    Regulation of Actin Filament Polymerization
You are here:
Chat with us!