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rabbit antibodies against psbe and psbf  (Agrisera)

 
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    Agrisera rabbit antibodies against psbe and psbf
    NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera <t>against</t> <t>PsbE</t> ( A ), <t>PsbF</t> ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.
    Rabbit Antibodies Against Psbe And Psbf, supplied by Agrisera, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit antibodies against psbe and psbf/product/Agrisera
    Average 90 stars, based on 1 article reviews
    rabbit antibodies against psbe and psbf - by Bioz Stars, 2026-04
    90/100 stars

    Images

    1) Product Images from "The N-terminal sequence of the extrinsic PsbP protein modulates the redox potential of Cyt b 559 in photosystem II"

    Article Title: The N-terminal sequence of the extrinsic PsbP protein modulates the redox potential of Cyt b 559 in photosystem II

    Journal: Scientific Reports

    doi: 10.1038/srep21490

    NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera against PsbE ( A ), PsbF ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.
    Figure Legend Snippet: NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera against PsbE ( A ), PsbF ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.

    Techniques Used:



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    rabbit antibodies against psbe and psbf  (Agrisera)
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    Agrisera rabbit antibodies against psbe and psbf
    NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera <t>against</t> <t>PsbE</t> ( A ), <t>PsbF</t> ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.
    Rabbit Antibodies Against Psbe And Psbf, supplied by Agrisera, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit antibodies against psbe and psbf/product/Agrisera
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    rabbit antibodies against psbe and psbf - by Bioz Stars, 2026-04
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    rabbit antibody against psbe  (Agrisera)
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    NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera <t>against</t> <t>PsbE</t> ( A ), <t>PsbF</t> ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.
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    rabbit antibodies against psbr, psbe, cp26  (Agrisera)
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    NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera <t>against</t> <t>PsbE</t> ( A ), <t>PsbF</t> ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.
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    rabbit antibodies against d2, psbr psbe  (Agrisera)
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    Cross-linking of PsbP with PSII membranes using EDC and sulfo-NHS. NaCl-washed PSII membranes were incubated with 6.25 mm EDC and 5 mm sulfo-NHS in either (A) the presence or (B) the absence of WT PsbP. Cross-linked proteins corresponding to 2 μg of Chl were loaded onto each lane. The proteins were immunodetected with antisera against CP47, CP43, <t>PsbO,</t> <t>D2,</t> D1, PsbP, PsbR, and <t>PsbE,</t> as shown on each lane. Protein size markers are shown on the left. C, NaCl-washed PSII was treated with 6.25 mm EDC and 5 mm sulfo-NHS to activate the carboxyl groups on the PSII. After activation, the PSII was washed and incubated either in the presence (+PsbP) or in the absence (−PsbP) of PsbP. As a positive control, the sample used in A was analyzed simultaneously.
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    rabbit antibodies against d2, psbr and psbe  (Agrisera)
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    Cross-linking of PsbP with PSII membranes using EDC and sulfo-NHS. NaCl-washed PSII membranes were incubated with 6.25 mm EDC and 5 mm sulfo-NHS in either (A) the presence or (B) the absence of WT PsbP. Cross-linked proteins corresponding to 2 μg of Chl were loaded onto each lane. The proteins were immunodetected with antisera against CP47, CP43, <t>PsbO,</t> <t>D2,</t> D1, PsbP, PsbR, and <t>PsbE,</t> as shown on each lane. Protein size markers are shown on the left. C, NaCl-washed PSII was treated with 6.25 mm EDC and 5 mm sulfo-NHS to activate the carboxyl groups on the PSII. After activation, the PSII was washed and incubated either in the presence (+PsbP) or in the absence (−PsbP) of PsbP. As a positive control, the sample used in A was analyzed simultaneously.
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    Image Search Results


    NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera against PsbE ( A ), PsbF ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.

    Journal: Scientific Reports

    Article Title: The N-terminal sequence of the extrinsic PsbP protein modulates the redox potential of Cyt b 559 in photosystem II

    doi: 10.1038/srep21490

    Figure Lengend Snippet: NaCl-washed PSII membranes were cross-linked with pN15 at a molar pN15:PSII ratio of 50:1 to 200:1. For each sample, an amount of protein corresponding to 3 μg Chl was loaded onto each lane and detected with antisera against PsbE ( A ), PsbF ( B ), PsbO ( C ), and D1 ( D ). The arrow at ~11 kDa indicates the peptide of pN15 cross-linked to PsbE. The dashed arrow at ~13 kDa indicates the putative peptide of PsbE cross-linked to PsbF. The original positions of PsbE (9 kDa), PsbF (4 kDa), PsbO (33 kDa), and D1 (32 kDa) subunits are also indicated.

    Article Snippet: Rabbit antibodies against PsbE and PsbF were purchased from Agrisera AB, Sweden.

    Techniques:

    Cross-linking of PsbP with PSII membranes using EDC and sulfo-NHS. NaCl-washed PSII membranes were incubated with 6.25 mm EDC and 5 mm sulfo-NHS in either (A) the presence or (B) the absence of WT PsbP. Cross-linked proteins corresponding to 2 μg of Chl were loaded onto each lane. The proteins were immunodetected with antisera against CP47, CP43, PsbO, D2, D1, PsbP, PsbR, and PsbE, as shown on each lane. Protein size markers are shown on the left. C, NaCl-washed PSII was treated with 6.25 mm EDC and 5 mm sulfo-NHS to activate the carboxyl groups on the PSII. After activation, the PSII was washed and incubated either in the presence (+PsbP) or in the absence (−PsbP) of PsbP. As a positive control, the sample used in A was analyzed simultaneously.

    Journal: The Journal of Biological Chemistry

    Article Title: The Conserved His-144 in the PsbP Protein Is Important for the Interaction between the PsbP N-terminus and the Cyt b 559 Subunit of Photosystem II *

    doi: 10.1074/jbc.M112.385286

    Figure Lengend Snippet: Cross-linking of PsbP with PSII membranes using EDC and sulfo-NHS. NaCl-washed PSII membranes were incubated with 6.25 mm EDC and 5 mm sulfo-NHS in either (A) the presence or (B) the absence of WT PsbP. Cross-linked proteins corresponding to 2 μg of Chl were loaded onto each lane. The proteins were immunodetected with antisera against CP47, CP43, PsbO, D2, D1, PsbP, PsbR, and PsbE, as shown on each lane. Protein size markers are shown on the left. C, NaCl-washed PSII was treated with 6.25 mm EDC and 5 mm sulfo-NHS to activate the carboxyl groups on the PSII. After activation, the PSII was washed and incubated either in the presence (+PsbP) or in the absence (−PsbP) of PsbP. As a positive control, the sample used in A was analyzed simultaneously.

    Article Snippet: Rabbit antibodies against D2, PsbR and PsbE were purchased from Agrisera.

    Techniques: Incubation, Activation Assay, Positive Control