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product information
|
| background |
|
PsbR protein is found in plant Photosystem II and anticipate to play a role in water oxidation, yet the physiological significance of PsbR has remained obscure. |
| immunogen |
|
KLH-conjugated synthetic peptide chosen from Arabidopsis thaliana PsbR P27202 |
| antibody format |
|
rabbit |
polyclonal |
|
serum, |
lyophilized |
|
| quantity |
|
100 µl, |
for reconstitution add 100 µl, 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 |
|
PSII antibody collection |
| additional information |
|
to be added when available |
application information
|
| recommended dilution |
|
1:15 000 with standard ECL (WB) |
| expected | apparent MW |
|
14 | 10 kDa |
| confirmed reactivity |
|
Arabidopsis thaliana, Nicotiana tabacum, Spinacia oleracea |
| predicted reactivity |
|
dicots including Brassica campestris, Solanum tuberosum, Vitis vinifera, monocots including Oryza sativa, Zea mays |
| not reactive in |
|
Chlamydomonas reinhardtii, Hordeum vulgare, Synechococcus sp. PCC 7942 |
| additional information |
|
not available at the moment |
| selected references |
|
not available yet |
|
application example 2 µg of total protein from (1) Arabidopsis thaliana leaf, (2) Horderum vulgare leaf ), (3) Chlamydomonas reinhardtii total cell , (4) Synechococcus sp. 7942 total cell were all extracted with PEB (AS08 300) and separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 1h to PVDF. Blots were blocked immediately following transfer in 2% ECL Advance blocking reagent (GE Healthcare) in 20 mM Tris, 137 mM sodium chloride pH 7.6 with 0.1% (v/v) Tween-20 (TBS-T) for 1h at room temperature with agitation. Blots were incubated in the primary antibody at a dilution of 1: 50 000 for 1h at room temperature with agitation. 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 TBS-T at room temperature with agitation. Blots were incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Abcam) diluted to 1:50 000 in 2% ECL Advance blocking solution for 1h at room temperature with agitation. The blots were washed as above and developed for 5 min with ECL Advance detection reagent according to the manufacturers instructions. Images of the blots were obtained using a CCD imager (FluorSMax, Bio-Rad) and Quantity One software (Bio-Rad). Exposure time was 1 second. |  |
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