SHOX antibody

Catalog No. ABIN2458012

Product Details anti-SHOX Antibody

Target: SHOX (Short Stature Homeobox (SHOX))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: 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 Details

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

Handling

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 Details for SHOX

Target: SHOX (Short Stature Homeobox (SHOX))

Alternative Name: SHOX (SHOX Products)

Synonyms: si:ch211-134k13.1 antibody, zgc:123182 antibody, GCFX antibody, PHOG antibody, SHOXY antibody, SS antibody, short stature homeobox antibody, shox antibody, SHOX antibody

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