ABHD5 Antikörper

Produktnummer ABIN7265357

Produktdetails anti-ABHD5 Antikörper

Target: ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser ABHD5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Verwendungszweck: ABHD5 Rabbit mAb

Kreuzreaktivität: Human, Ratte

Produktmerkmale: Monoclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: A synthesized peptide derived from human ABHD5

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,0.05 % BSA,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: Store at -20°C. Avoid freeze / thaw cycles.

Details zu ABHD5

Target: ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))

Andere Bezeichnung: ABHD5 (ABHD5 Produkte)

Synonyme: ABHD5 antikoerper, cds antikoerper, cgi58 antikoerper, iecn2 antikoerper, ncie2 antikoerper, abhd5 antikoerper, CDS antikoerper, CGI58 antikoerper, IECN2 antikoerper, NCIE2 antikoerper, 1300003D03Rik antikoerper, 2010002J10Rik antikoerper, CGI-58 antikoerper, IECN5 antikoerper, abhydrolase domain containing 5 antikoerper, abhydrolase domain containing 5a antikoerper, abhydrolase domain containing 5 L homeolog antikoerper, ABHD5 antikoerper, abhd5 antikoerper, abhd5a antikoerper, Abhd5 antikoerper, abhd5.L antikoerper

Hintergrund: The protein encoded by this gene belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in this gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation. [provided by RefSeq, Jul 2008],CDS, CGI58, IECN2, NCIE2,Cancer,Cardiovascular,Endocrine & Metabolism,Endocrine and metabolic diseases,Endocrine and metabolic diseases_Obesity,Lipid Metabolism,Lipids,Lipids_Adipose Related,Lipids_Fatty Acids,Signal Transduction,ABHD5

Molekulargewicht: 45kDa

Gen-ID: 51099

UniProt: Q8WTS1

Pathways: Lipid Metabolism