SHOX anticorps

N° du produit ABIN2458012

Détail du produit anti-SHOX anticorps

Antigène: SHOX (Short Stature Homeobox (SHOX))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SHOX est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SHOX.

Information d'application

Indications d'application: 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

Stockage

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.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

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

Détails sur SHOX

Antigène: SHOX (Short Stature Homeobox (SHOX))

Autre désignation: SHOX (SHOX Produits)

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

Sujet: 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.

Poids moléculaire: 32 kDa

ID gène: 6473

NCBI Accession: NP_000442

UniProt: O15266