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

N° du produit ABIN7870295

Cet anticorps Lapin Polyclonal détecte spécifiquement Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 dans WB, ELISA, FACS et IHC (p). Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 (HDHD5) (AA 12-423) anticorps (ABIN7870295)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Inconjugué

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

Détail du produit

Épitope: AA 12-423

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

Purification: Antigen affinity chromatography

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

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the HDHD5 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

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

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détail du antigène

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

Autre désignation: HDHD5

Sujet: 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