MCCC2 Antikörper

Produktnummer ABIN7116246

Produktdetails anti-MCCC2 Antikörper

Target: MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MCCC2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Aufreinigung: Immunogen affinity purified

Reinheit: ≥95 % as determined by SDS-PAGE

Immunogen: methylcrotonoyl-Coenzyme A carboxylase 2 (beta)

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB: 1:500 - 1:2000, IHC: 1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

Haltbarkeit: 12 months

Details zu MCCC2

Target: MCCC2 (Methylcrotonoyl-CoA Carboxylase 2 (Beta) (MCCC2))

Andere Bezeichnung: MCCC2 (MCCC2 Produkte)

Synonyme: si:dkey-57m14.1 antikoerper, zgc:85685 antikoerper, MCCB antikoerper, 3-METHYLCROTONYL-COA CARBOXYLASE antikoerper, 3-methylcrotonyl-CoA carboxylase antikoerper, F28A23.210 antikoerper, F28A23_210 antikoerper, 4930552N12Rik antikoerper, methylcrotonoyl-CoA carboxylase 2 (beta) antikoerper, methylcrotonoyl-CoA carboxylase 2 antikoerper, methylcrotonoyl-CoA carboxylase 2 S homeolog antikoerper, 3-methylcrotonyl-CoA carboxylase antikoerper, methylcrotonoyl-Coenzyme A carboxylase 2 (beta) antikoerper, mccc2 antikoerper, MCCC2 antikoerper, mccc2.S antikoerper, Mccc2 antikoerper, MCCB antikoerper

Hintergrund: Synonyms:MCCB Background:This gene encodes the small subunit of 3-methylcrotonyl-CoA carboxylase. This enzyme functions as a heterodimer and catalyzes the carboxylation of 3-methylcrotonyl-CoA to form 3-methylglutaconyl-CoA. Mutations in this gene are associated with 3-Methylcrotonylglycinuria, an autosomal recessive disorder of leucine catabolism.

Molekulargewicht: 61 kDa

Gen-ID: 64087

UniProt: Q9HCC0