HOXA13 anticorps

N° du produit ABIN2460332

Détail du produit anti-HOXA13 anticorps

Antigène: HOXA13 (Homeobox A13 (HOXA13))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HOXA13 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 HOXA13.

Information d'application

Indications d'application: HOXA13 antibody can be used for detection of HOXA13 by ELISA at 1:312500. HOXA13 antibody can be used for detection of HOXA13 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 HOXA13 antibody at -20 °C.

Détails sur HOXA13

Antigène: HOXA13 (Homeobox A13 (HOXA13))

Autre désignation: HOXA13 (HOXA13 Produits)

Synonymes: anticorps HOXA13, anticorps RGD1562483, anticorps HOX1, anticorps HOX1J, anticorps Hd, anticorps Hox-1.10, anticorps homeobox A13, anticorps homeo box A13, anticorps HOXA13, anticorps Hoxa13

Sujet: In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome. In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. Expansion of a polyalanine tract in the encoded protein can cause hand-foot-uterus syndrome, also known as hand-foot-genital syndrome. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Poids moléculaire: 40 kDa

ID gène: 3209

NCBI Accession: NP_000513

UniProt: P31271