SHOX2 anticorps (AA 37-87)

N° du produit ABIN8124660

L’anticorps anti-SHOX2 Polyclonal Lapin est utilisé pour la détection de SHOX2 dans des échantillons de Humain, Rat et Souris. Il a été validé pour WB, IHC et FACS.

Aperçu rapide pour SHOX2 anticorps (AA 37-87) (ABIN8124660)

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

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SHOX2 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Détail du produit anti-SHOX2 anticorps

Épitope: AA 37-87

Fonction: SHOX2 Antibody

Specificité: This antibody detects endogenous levels of SHOX2 at Human/Mouse/Rat

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogène: Synthesized peptide derived from human SHOX2 AA range: 37-87

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-2000,IHC 1:50-300,FCM 1:100-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C/1 year

Date de péremption: 12 months

Détails sur SHOX2

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

Autre désignation: SHOX2

Sujet:

Background: This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox 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 homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009],

Gene Name: SHOX2 OG12X SHOT

Protein Name: SHOX2

ID gène: 6474

UniProt: O60902

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