Homeobox D13 antibody (Middle Region)

Catalog No. ABIN952786

Product Details anti-Homeobox D13 Antibody

Target: Homeobox D13 (HOXD13)

Binding Specificity: AA 201-230, Middle Region

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Homeobox D13 antibody is un-conjugated

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Specificity: This antibody recognizes Human and Mouse HOXD13 / HOX4I (C-term).

Purification: Protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 201-230 amino acids from the Central region of human HOXD13 / HOX4I

Isotype: Ig Fraction

Application Details

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

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS containing 0.09 % (W/V) Sodium Azide as preservative

Preservative: Sodium azide

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

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

Storage Comment: Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.

Target Details for Homeobox D13

Target: Homeobox D13 (HOXD13)

Alternative Name: HOXD13 / HOX4I (HOXD13 Products)

Synonyms: XHoxd13 antibody, BDE antibody, BDSD antibody, HOX4I antibody, SPD antibody, Hox-4.8 antibody, spdh antibody, hoxd-13 antibody, hoxd13 antibody, zgc:110511 antibody, homeobox D13 antibody, homeobox D13 S homeolog antibody, homeobox D13a antibody, homeo box D13 antibody, HOXD13 antibody, hoxd13.S antibody, Hoxd13 antibody, hoxd13a antibody

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.Synonyms: Homeobox protein Hox-D13, Hox-4I

Molecular Weight: 36101 Da

Gene ID: 3239

NCBI Accession: NP_000514

Pathways: Synaptic Membrane