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Anti-HAX1 antibody (ab81973)

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Overview

Product name

Anti-HAX1 antibody
See all HAX1 products (4) ...

Description

Goat polyclonal to HAX1

Specificity

ab81973 is expected to recognize both reported isoforms (NP_006109.2 and NP_001018238.1).

Tested applications

WB, ELISAmore details

Cross reactivity

Reacts with

Human

Immunogen

Synthetic peptide: C-TRHEADSSPRGDPES, corresponding to internal sequence amino acids 241-255 of human HAX1 according to NP_006109.2 (or 193-207 of NP_001018238.1).

C-TRHEADSS PRGDPES

Positive control

Human kidney, liver and testis lysates.

Properties

Form

Liquid

Storage instructions

Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid repeated freeze / thaw cycles.

Storage buffer

Preservative: 0.02% Sodium Azide
Constituents: 0.5% BSA, Tris saline, pH 7.3

Concentration

Concentration information loading...

Purity

Immunogen affinity purified

Purification notes

Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.

Clonality

Polyclonal

Isotype

IgG

  • Western blot - HAX1 antibody (ab81973)Western blot - HAX1 antibody (ab81973) image (enlarge)

Applications

Show applications key

Our Abpromise guarantee covers the use of ab81973 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application notes

Peptide ELISA: antibody detection limit dilution 1:2,000.
WB: Use at a concentration of 1 - 3 µg/ml. Predicted molecular weight: 32 kDa.

Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.

Target

Relevance

HAX1 associates with HS1, binding to its N-terminal region. It is also known to associate with PKD2 (involved in polycystic kidney disease) and with cortactin/EMS1. 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.

Cellular localization

Endoplasmic reticulum, Mitochondrial and Nuclear membrane. Note: Predominantly mitochondrial, but also to a lesser extent in endoplasmic reticulum and nuclear envelope.

Alternative names

  • FLJ17042 antibody
  • FLJ18492 antibody
  • FLJ93803 antibody
  • HAX 1 antibody
  • Hax1a antibody
  • HCLS1 and PKD2 associated protein antibody
  • HCLS1 associated protein antibody
  • HCLS1 associated protein X 1 antibody
  • HCLSBP1 antibody
  • HS 1 associated protein X 1 antibody
  • HS 1 binding protein antibody
  • HS1 associating protein X 1 antibody
  • HS1 binding protein 1 antibody
  • HS1 binding protein antibody
  • HS1BP1 antibody
  • OTTHUMP00000034190 antibody
  • SCN3 antibody
see all

Anti-HAX1 antibody images:

  Western blot - HAX1 antibody (ab81973)

Western blot - HAX1 antibody (ab81973)

Anti-HAX1 antibody (ab81973) at 1 µg/ml + human testis lysate in RIPA buffer at 35 µg
developed using the ECL technique

Predicted band size : 32 kDa
Observed band size : 32 kDa


Exposure time : 1 hour

References for Anti-HAX1 antibody (ab81973)

ab81973 has not yet been referenced specifically in any publications.

Publishing research using ab81973? Please let us know so that we can cite the reference in this datasheet

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"