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SHOX antibody

This Rabbit Polyclonal antibody specifically detects SHOX in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN2458012

Quick Overview for SHOX antibody (ABIN2458012)

Target

See all SHOX Antibodies
SHOX (Short Stature Homeobox (SHOX))

Reactivity

  • 17
  • 4
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 15
  • 2
Rabbit

Clonality

  • 17
Polyclonal

Conjugate

  • 12
  • 1
  • 1
  • 1
  • 1
  • 1
This SHOX antibody is un-conjugated

Application

Western Blotting (WB), ELISA
  • Purification

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SHOX.
  • Application Notes

    SHOX antibody can be used for detection of SHOX by ELISA at 1:312500. SHOX antibody can be used for detection of SHOX by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Concentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handling Advice

    As with any antibody avoid repeat freeze-thaw cycles.

    Storage

    4 °C/-20 °C

    Storage Comment

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store SHOX antibody at -20 °C.
  • Target

    SHOX (Short Stature Homeobox (SHOX))

    Alternative Name

    SHOX

    Background

    This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies.This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

    Molecular Weight

    32 kDa

    Gene ID

    6473

    NCBI Accession

    NP_000442

    UniProt

    O15266
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