Zeaxanthin Epoxidase (ZEP) Antikörper

Antigen: Zeaxanthin Epoxidase (ZEP)

Synonyme: ABA DEFICIENT 1, ABA1, ARABIDOPSIS THALIANA ABA DEFICIENT 1, ARABIDOPSIS THALIANA ZEAXANTHIN EPOXIDASE, ATABA1, ATZEP, IBS3, IMPAIRED IN BABA-INDUCED STERILITY 3, K8A10.10, K8A10_10, LOS6, LOW EXPRESSION OF OSMOTIC STRESS-RESPONSIVE GENES 6, NON-PHOTOCHEMICAL QUENCHING 2, NPQ2, ZEAXANTHIN EPOXIDASE, ZEP

Klonalität: Polyklonal

Wirt: Kaninchen

Reaktivität: Arabidopsis thaliana

Applikation: Western Blot (WB)

Produktnummer: ABIN249372

Produktbeschreibung

Immunogen: KLH-conjugated synthetic peptide derived from ZEP sequence of Arabidopsisthaliana Q9FGC7

Format: Lyophilized

Beschreibung: Zeaxanthin Epoxidase (ZEP) catalyses the O2-/NAPDHdependent epoxidation ofzeaxanthin to violaxanthin via antheraxanthin at the stromal side of the thylakoidmembrane of green plants. ZEP also functions in the first step of the biosynthesisof the abiotic stress hormone abscisic acid (ABA).

Spezifität: Predicted reactivity: dicots including: Brassica rapa, Vitis vinifera. Not reactive in: Spinacia oleracea.

Synonyme: ABA DEFICIENT 1, ABA1, ARABIDOPSIS THALIANA ABA DEFICIENT 1, ARABIDOPSIS THALIANA ZEAXANTHIN EPOXIDASE, ATABA1, ATZEP, IBS3, IMPAIRED IN BABA-INDUCED STERILITY 3, K8A10.10, K8A10_10, LOS6, LOW EXPRESSION OF OSMOTIC STRESS-RESPONSIVE GENES 6, NON-PHOTOCHEMICAL QUENCHING 2, NPQ2, ZEAXANTHIN EPOXIDASE, ZEP

Anwendungen

Applikationshinweise: Recommended Dilution 1:1000 € 1:5000 with standard ECL (WB).

Reinheit: Serum

Lagerung: store lyophilized/reconstituted at -20°C, once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior toopening them to avoid any losses that might occur from lyophilized materialadhering to the cap or sides of the tubes.

Forschungsgebiet: Pflanzenphysiologie

Beschränkungen: Nur für Forschungszwecke einsetzbar

Bilder

10 ug of total leaf protein from (1) A.thaliana leafs isolated with PEB (see product AS08 300) and A.thaliana chloroplasts (2) and thylakoids (3) where separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 60 min (30V) to nitrocellulose. Filters where blocked 1h with 2% low-fat milk powder in TBS-T (0.1% TWEEN 20) and probed with AS08 289 (1:1000, 1h) and secondary anti-rabbit (1:20000, 1 h) antibody (HRP conjugated, Abcam) in TBS-T containing 2% low fat milk powder. Antibody incubations where followed by washings in TBS-T (15, +5, +5, +5 min). All steps were performed at RT with agitation. Signal was detected with standard ECL (Invitrogen) using a Fuji LAS-3000 CCD (150s, standard sensitivity).