HOXD1 antibody

Catalog No. ABIN2457968

The Rabbit Polyclonal anti-HOXD1 antibody has been validated for WB and ELISA. It is suitable to detect HOXD1 in samples from Human, Mouse and Rat.

Quick Overview for HOXD1 antibody (ABIN2457968)

Target: HOXD1 (Homeobox D1 (HOXD1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HOXD1 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-HOXD1 Antibody

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human HOXD1.

Application Details

Application Notes: HOXD1 antibody can be used for detection of HOXD1 by ELISA at 1:312500. HOXD1 antibody can be used for detection of HOXD1 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 HOXD1 antibody at -20 °C.

Target Details for HOXD1

Target: HOXD1 (Homeobox D1 (HOXD1))

Alternative Name: HOXD1

Background: HOXD1 is a protein with a homeobox DNA-binding domain, and it belongs to the Antp homeobox family. This nuclear protein functions as a sequence-specific transcription factor that is involved in differentiation and limb development. Mutations in this gene have been associated with severe developmental defects on the anterior-posterior (a-p) limb axis.This gene is a member of the Antp homeobox family and encodes a protein with a homeobox DNA-binding domain. This nuclear protein functions as a sequence-specific transcription factor that is involved in differentiation and limb development. Mutations in this gene have been associated with severe developmental defects on the anterior-posterior (a-p) limb axis. 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: 34 kDa

Gene ID: 3231

NCBI Accession: NP_078777

UniProt: Q9GZZ0