HOXA13 antibody

Catalog No. ABIN2460332

Product Details anti-HOXA13 Antibody

Target: HOXA13 (Homeobox A13 (HOXA13))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HOXA13 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 HOXA13.

Application Details

Application Notes: 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

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 HOXA13 antibody at -20 °C.

Target Details for HOXA13

Target: HOXA13 (Homeobox A13 (HOXA13))

Alternative Name: HOXA13 (HOXA13 Products)

Synonyms: HOXA13 antibody, RGD1562483 antibody, HOX1 antibody, HOX1J antibody, Hd antibody, Hox-1.10 antibody, homeobox A13 antibody, homeo box A13 antibody, HOXA13 antibody, Hoxa13 antibody

Background: 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.

Molecular Weight: 40 kDa

Gene ID: 3209

NCBI Accession: NP_000513

UniProt: P31271