Homeobox D13 antibody (AA 202-230)

Catalog No. ABIN655171

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

Quick Overview for Homeobox D13 antibody (AA 202-230) (ABIN655171)

Target: Homeobox D13 (HOXD13)

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Homeobox D13 antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB19191

Product Details anti-Homeobox D13 Antibody

Binding Specificity: AA 202-230

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This HOXD13 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 202-230 amino acids from the Central region of human HOXD13.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Storage Comment: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Expiry Date: 6 months

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.

Molecular Weight: 36101

Gene ID: 3239

NCBI Accession: NP_000514

UniProt: P35453

Pathways: Synaptic Membrane