DLX3 antibody (AA 71-120)

Catalog No. ABIN1533520

The Rabbit Polyclonal anti-DLX3 antibody is suitable to detect DLX3 in samples from Human and Mouse. It has been validated for WB, IHC, ELISA and IF.

Quick Overview for DLX3 antibody (AA 71-120) (ABIN1533520)

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

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DLX3 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Product Details anti-DLX3 Antibody

Binding Specificity: AA 71-120

Purpose: Dlx-3 Antibody

Specificity: Dlx-3 Polyclonal Antibody detects endogenous levels of Dlx-3 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Purity: > 95 %

Immunogen: The antiserum was produced against synthesized peptide derived from human DLX3. AA range:71-120

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for DLX3

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

Alternative Name: DLX3

Background:

Synonyms: DLX3, Homeobox protein DLX-3

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. [provided by RefSeq, Jul 2008],

Gene Name: DLX3

Protein Name: Homeobox protein DLX-3

Molecular Weight: 31 kDa

Gene ID: 1747

OMIM: 600525

UniProt: O60479