DLX3 antibody

Catalog No. ABIN7266800

Product Details anti-DLX3 Antibody

Target: DLX3 (Distal-Less Homeobox 3 (DLX3))

Reactivity: Human

Host: Rabbit

Clonality: Monoclonal

Conjugate: This DLX3 antibody is un-conjugated

Application: Western Blotting (WB)

Purpose: DLX3 Rabbit mAb

Cross-Reactivity: Human, Mouse

Characteristics: Monoclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant protein of Human DLX3.

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

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: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for DLX3

Target: DLX3 (Distal-Less Homeobox 3 (DLX3))

Alternative Name: DLX3 (DLX3 Products)

Synonyms: AI4 antibody, TDO antibody, AV237891 antibody, Dlx-3 antibody, DLX3 antibody, ai4 antibody, tdo antibody, xdlx3 antibody, MGC69301 antibody, dll2 antibody, dlx3 antibody, dlx-3 antibody, id:ibd3531 antibody, wu:fb83f11 antibody, zgc:91827 antibody, distal-less homeobox 3 antibody, distal-less homeobox 3 L homeolog antibody, distal-less homeobox 3b antibody, DLX3 antibody, Dlx3 antibody, dlx3 antibody, dlx3.L antibody, dlx3b antibody

Background: Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism.,DLX3,AI4,TDO,Epigenetics & Nuclear Signaling,Transcription Factors,DLX3

Molecular Weight: 31kDa

Gene ID: 1747

UniProt: O60479