FAHD2A Antikörper (AA 121-230) (Cy5)

Produktnummer ABIN896010

Dieses Anti-FAHD2A-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von FAHD2A in WB, IF (cc) und IF (p). Geeignet für Human.

Kurzübersicht für FAHD2A Antikörper (AA 121-230) (Cy5) (ABIN896010)

Target: FAHD2A (Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FAHD2A Antikörper ist konjugiert mit Cy5

Applikation: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Produktdetails anti-FAHD2A Antikörper (Cy5)

Bindungsspezifität: AA 121-230

Homologie: Human,Mouse,Rat,Horse,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FAHD2A

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu FAHD2A

Target: FAHD2A (Fumarylacetoacetate Hydrolase Domain Containing 2A (FAHD2A))

Andere Bezeichnung: FAHD2A

Hintergrund:

Synonyms: CGI 105, FAH2A_HUMAN, FAHD 2A, FAHD2A, Fumarylacetoacetate hydrolase domain containing 1, Fumarylacetoacetate hydrolase domain containing 2A, Fumarylacetoacetate hydrolase domain containing protein 2A, Fumarylacetoacetate hydrolase domain-containing protein 2A.

Background: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is also associated with mutations to chromosome 2.

Gen-ID: 51011