Homeobox D13 antibody

Catalog No. ABIN7466505

This Rabbit Polyclonal antibody specifically detects Homeobox D13 in WB. It exhibits reactivity toward Human.

Quick Overview for Homeobox D13 antibody (ABIN7466505)

Target: Homeobox D13 (HOXD13)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Homeobox D13 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-Homeobox D13 Antibody

Cross-Reactivity: Human

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human HOXD13. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: Jurkat , Raji , NCI-H929

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300

Preservative: ProClin

Precaution of Use: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for Homeobox D13

Target: Homeobox D13 (HOXD13)

Alternative Name: homeobox D13

Background: Homeobox D13 , BDE , BDSD , HOX4I , SPD , SPD1,This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq]

Molecular Weight: 36 kDa

Gene ID: 3239

UniProt: P35453

Pathways: Synaptic Membrane