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

Produktnummer ABIN7870295

Dieser Kaninchen Polyklonal Antikörper detektiert spezifisch Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 in WB, ELISA, FACS und IHC (p). Es zeigt Reaktivität gegenüber Proben von Human, Maus und Ratte.

Kurzübersicht für Haloacid Dehalogenase-Like Hydrolase Domain-Containing 5 (HDHD5) (AA 12-423) Antikörper (ABIN7870295)

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

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Unkonjugiert

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

Produktdetails

Bindungsspezifität: AA 12-423

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

Aufreinigung: Antigen affinity chromatography

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

Isotyp: IgG

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Lyophilized

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

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: 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.

Antigendetails

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

Andere Bezeichnung: HDHD5

Hintergrund: 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