AGPS Antikörper (AA 379-658)

Produktnummer ABIN6136644

Dieses Anti-AGPS-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von AGPS in WB. Geeignet für Human.

Kurzübersicht für AGPS Antikörper (AA 379-658) (ABIN6136644)

Target: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser AGPS Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-AGPS Antikörper

Bindungsspezifität: AA 379-658

Sequenz: IKIRPVPEYQ KYGSVAFPNF EQGVACLREI AKQRCAPASI RLMDNKQFQF GHALKPQVSS IFTSFLDGLK KFYITKFKGF DPNQLSVATL LFEGDREKVL QHEKQVYDIA AKFGGLAAGE DNGQRGYLLT YVIAYIRDLA LEYYVLGESF ETSAPWDRVV DLCRNVKERI TRECKEKGVQ FAPFSTCRVT QTYDAGACIY FYFAFNYRGI SDPLTVFEQT EAAAREEILA NGGSLSHHHG VGKLRKQWLK ESISDVGFGM LKSVKEYVDP NNIFGNRNLL

Kreuzreaktivität: Human, Maus

Produktmerkmale: Polyclonal Antibodies

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 379-658 of human AGPS (NP_003650.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:1000 - 1:2000

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,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 AGPS

Target: AGPS (Alkylglycerone Phosphate Synthase (AGPS))

Andere Bezeichnung: AGPS

Hintergrund: This gene is a member of the FAD-binding oxidoreductase/transferase type 4 family. It encodes a protein that catalyzes the second step of ether lipid biosynthesis in which acyl-dihydroxyacetonephosphate (DHAP) is converted to alkyl-DHAP by the addition of a long chain alcohol and the removal of a long-chain acid anion. The protein is localized to the inner aspect of the peroxisomal membrane and requires FAD as a cofactor. Mutations in this gene have been associated with rhizomelic chondrodysplasia punctata, type 3 and Zellweger syndrome.,AGPS,ADAP-S,ADAS,ADHAPS,ADPS,ALDHPSY,RCDP3,Neuroscience,AGPS

Molekulargewicht: 72 kDa

Gen-ID: 8540

UniProt: O00116

Pathways: SARS-CoV-2 Protein Interaktom