Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 (HDHD5) (AA 12-423) antibody

Catalog No. ABIN7870295

This Rabbit Polyclonal antibody specifically detects Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 in WB, ELISA, FACS and IHC (p). It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 (HDHD5) (AA 12-423) antibody (ABIN7870295)

Target: Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 (HDHD5)

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: Un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details

Binding Specificity: AA 12-423

Purpose: HDHD5 Antibody / Haloacid dehalogenase-like hydrolase domain-containing 5

Purification: Antigen affinity chromatography

Immunogen: An E.coli-derived human recombinant protein (amino acids A12-E423) was used as the immunogen for the HDHD5 antibody.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the HDHD5 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: After reconstitution, the HDHD5 Antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Target Details

Target: Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 (HDHD5)

Alternative Name: HDHD5

Background: Haloacid dehalogenase-like hydrolase domain-containing 5 (HDHD5), also called Cat eye syndrome critical region protein 5 (CECR5), is a candidate gene for the Cat Eye Syndrome (CES), a developmental disorder associated with the duplication of a 2 Mb region of 22q11.2. Duplication usually takes in the form of a surpernumerary bisatellited isodicentric chromosome, resulting in four copies of the region (represents an inv dup22(q11)). CES is characterized clinically by the combination of coloboma of the iris and anal atresia with fistula, downslanting palpebral fissures, preauricular tags and/or pits, frequent occurrence of heart and renal malformations, and normal or near-normal mental development. [UniProt]

UniProt: Q9BXW7