Homeobox D13 antibody (N-Term)

Catalog No. ABIN5516975

This anti-Homeobox D13 antibody is a Rabbit Polyclonal antibody detecting Homeobox D13 in WB. Suitable for Human.

Quick Overview for Homeobox D13 antibody (N-Term) (ABIN5516975)

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

Binding Specificity: N-Term

Sequence: ASGFAYPGTS ERTGSSSSSS SSAVVAARPE APPAKECPAP TPAAAAAAPP

Characteristics: This is a rabbit polyclonal antibody against HXD13. It was validated on Western Blot.

Purification: Affinity purified

Immunogen: The immunogen for Anti-HOXD13 antibody is: synthetic peptide directed towards the N-terminal region of Human HXD13

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

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

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for Homeobox D13

Target: Homeobox D13 (HOXD13)

Alternative Name: HOXD13

Background: 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.

Alias Symbols: BDE, SPD, BDSD, HOX4I

Protein Size: 343

Gene ID: 3239

NCBI Accession: NP_000514

UniProt: P35453

Pathways: Synaptic Membrane