SHOX2 anticorps

N° du produit ABIN2460684

Cet anticorps anti-SHOX2 est un anticorps Lapin Polyclonal détectant SHOX2 dans WB et ELISA. Adapté pour Humain, Rat, Souris, Chien et Poisson zèbre (Danio rerio).

Aperçu rapide pour SHOX2 anticorps (ABIN2460684)

Antigène: SHOX2 (Short Stature Homeobox 2 (SHOX2))

Reactivité: Humain, Rat, Souris, Chien, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SHOX2 est non-conjugé

Application: Western Blotting (WB), ELISA

Détail du produit anti-SHOX2 anticorps

Purification: Antibody is purified by protein A chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SHOX2.

Information d'application

Indications d'application: SHOX2 antibody can be used for detection of SHOX2 by ELISA at 1:62500. SHOX2 antibody can be used for detection of SHOX2 by western blot at 2.5 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 100 ?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 SHOX2 antibody at -20 °C.

Détails sur SHOX2

Antigène: SHOX2 (Short Stature Homeobox 2 (SHOX2))

Autre désignation: SHOX2

Sujet: SHOX2 is a member of the homeo box family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeo box genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeo box genes. SHOX is a pseudoautosomal homeo box gene that is thought to be responsible for idiopathic short stature and implicated to play a role in the short stature phenotype of Turner syndrome patients.

Poids moléculaire: 35 kDa

ID gène: 6474

NCBI Accession: NP_006875

UniProt: O60902

Pathways: Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development