PSA3 | Photosystem I Assembly 3

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AS15 2872  | Clonality: Polyclonal  |  Host: Rabbit  |  Reactivity: Zea mays


29 st
Item No:
AS15 2872

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product information
Background PSA3 (Photosystem I Assembly 3) is involved in promotion of photosystem I biogenesis in angiosperms. It is a nucleus-encoded protein.
Immunogen Recombinant PSA3, amino acids 110 to 269 derived from Zea mays  Zm00001d013295
Host Rabbit
Clonality Polyclonal
Purity Affinity purified serum in PBS, pH 7.4
Format Lyophilized

50 µg

Reconstitution For reconstitution add 50 ĩl, of sterile water.
Storage Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles.Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.
Tested applications Western blot (WB)
Related products Collection of antibodies to PSI

Plant and algal protein extraction buffer

Secondary antibodies

Additional information
application information
Recommended dilution 1 : 2000 (WB)
Expected | apparent MW 26 kDa
Confirmed reactivity Zea mays
Predicted reactivity
Not reactive in No confirmed exceptions from predicted reactivity are currently known.
Additional information
Selected references Shen J, Williams-Carrier R, and Barkan A. (2017) PSA3, a protein on the stromal face of the thylakoid membrane, promotes photosystem I accumulation in cooperation with the assembly factor PYG7. Plant Physiol. 2017 Jul;174(3):1850-1862. doi: 10.1104/pp.17.00524.

Application example

western blot using anti-PSA3 antibodies

5 µg of total protein from Zea mays leaf seedling tissue was extracted with protein extraction buffer (100 mM Tris pH7.5, 10% glycerol, 1 mM EDTA, 1mM EGTA, 2mM pMSF, 0.002 mg leupeptin, 0.002 mg pepstatin A, 2.5 mM DTT) and denatured in 1XPSB (33 mM Tris pH 6.8, 50 mM 2-Mercaptoethanol, 2% SDS, 10% glycerol, 0.1% bromophenol blue) at 70°C for 5 min, separated on 4-15% Tris-Glycine SDS-PAGE and blotted overnight to nitrocellulose using tank transfer. Blots were blocked with 4% milk in 1XTBST for 1h at room temperature (RT) with agitation. The blot was incubated in the primary antibody at a dilution of 1:2000 for 1h at RT with agitation in TBST. The antibody solution was decanted and the blot was rinsed briefly twice, then washed once for 15 min and 3 times for 5 min in TBST at RT with agitation. The blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated) diluted to 1:10 000 for 1h at RT with agitation. The blot was washed as above and developed for 2 min with chemiluminescent detection reagent.

Courtesy Dr. Alice Barkan, University of Oregon, USA

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