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Rubisco | 557 kDa hexadecamer

AS07 218 | Clonality: Polyclonal  |  Host: Rabbit  |  Reactivity: higher plants, lichens, algae
Rubisco | 557 kDa hexadecamer in the group Antibodies Plant/Algal  / Photosynthesis  / RUBISCO/Carbon metabolism at Agrisera AB (Antibodies for research) (AS07 218)
Rubisco | 557 kDa hexadecamer



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Product name, number (Agrisera, Sweden)

Data sheet Product citations Protocols Add review

Product Information

Immunogen

purified 557 kDa hexadecamer Rubisco protein complex from Spinacia oleracea (SIGMA-ALDRICH R-8000), UniProt: P00875 and Q43832

Host Rabbit
Clonality Polyclonal
Purity Serum
Format Lyophilized
Quantity 50 ĩl
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 the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.
Tested applications Immunolocalization (IL), Western blot (WB)
Recommended dilution 1 : 10 000-1 : 20 000 on 0,5-10 ug total cellular protein/lane and standard (WB), 1 : 500-1:1000 (IL)
Expected | apparent MW

53-55 | 53-55 kDa

Reactivity

Confirmed reactivity Anabaena sp. PCC 7120, Arabidopsis thaliana, Aucuba japonica, Fremyella diplosiphon, Glycine max, Hordeum vulgare, Manihot esculenta Crantz, Oryza sativa, Physcomitrium patens, Pisum sativum, Populus sp., Salsola laricifolia, Solanum tuberosum, Spinacia oleracea, Synechocystis sp. PCC 6803, Synechococcus sp. PCC7942, Zea mays
Predicted reactivity higher plants, algae, Nannochloropsis sp.
Not reactive in Chlamydomonas reinhardtii (immulolocalization)

Application examples

Application examples Application example

0.5 µg of total leaf protein isolated with Agrisera Protein Eextraction Buffer (AS08 300) from Arabidopsis thaliana (1), Spinacia oleracea (2), Zea mays (3), Hordeum vulgare (4), Solanum tuberosum (5), Pisum sativum (6) were separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 45 min (30V) to nitrocellulose.  Filters where blocked 1h with 2% low-fat milk powder in TBS-T (0.1% TWEEN 20) and probed with AS07 218 (1:20 000, 1h) and secondary anti-rabbit (1:20000, 1 h) antibody (HRP conjugated) 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 chemiluminescence using a Fuji LAS-3000 CCD (300s, high sensitivity).

Reactant: Manihot esculenta (Cassava)

Application: Western Blotting

Pudmed ID: 20187967

Journal: Proteome Sci

Figure Number: 5A

Published Date: 2010-02-27

First Author: Li, K., Zhu, W., et al.

Impact Factor: 2.037

Open Publication

Western blotting of Rubisco and ?-tubulan. Rubisco and ?-tubulan in the somatic embryos, plantlets and tuberous roots of cassava cultivar SC8 were detected by Western blotting using antiRubisco-polyclonal antibody from Agrisera (AS07218) and anti-?-tubulin-monoclonal antibody from Sigma-Aldrich (T9026). ARs, adventitious roots.


Reactant: Manihot esculenta (Cassava)

Application: Western Blotting

Pudmed ID: 24727655

Journal: PLoS One

Figure Number: 5A

Published Date: 2014-04-15

First Author: An, F., Fan, J., et al.

Impact Factor: 2.942

Open Publication

Western blotting of Rubisco, APX and PrxQ.The expression of Rubisco, APX and PrxQ in leaves of cassava NZ199 diploid (a) and autotetraploid (b) genotypes were detected by western blotting using antiRubisco-polyclonal antibody (AS07218), anti-APX antibody (AS08368) and anti-PrxQ antibody (AS05093) from Agrisera, respectively.


Reactant: Manihot esculenta (Cassava)

Application: Western Blotting

Pudmed ID: 27881899

Journal: Plant Mol Biol Report

Figure Number: 8A

Published Date: 2016-11-25

First Author: An, F., Li, G., et al.

Impact Factor: 1.526

Open Publication

Western blotting of Rubisco and peroxiredoxin. The expressions of Rubisco (a) and peroxiredoxin (b) in apical expanded leaves of SC8and Col1046 were detected by Western blotting using anti-Rubisco polyclonal antibody (AS07218) and anti-peroxiredoxin antibody (AS05093) from Agrisera, respectively. Mr, protein marker; lines a and b, the expression of Rubisco and peroxiredoxin of SC8 in 5 °C for 0 and 10 days, respectively; lines c and d, the expression of Rubisco and peroxiredoxin of Co11046 in 5 °C for 0 and 10 days, respectively


Reactant: Synechocystis

Application: Western Blotting

Pudmed ID: 31143173

Journal: Front Microbiol

Figure Number: 7A

Published Date: 2019-05-31

First Author: Oh, S. & Montgomery, B. L.

Impact Factor: 5.259

Open Publication

Accumulation of OCP protein in WT and phycobilisome-deficient strains. Immunoblot analysis was performed using anti-OCP antibody (top panels) or anti-RbcL antibody (bottom panels), with representative blots shown. Total soluble proteins were extracted from wild-type (WT), ?cpcF and ?cpcG1 strains (two independent mutant strains for each ?cpcF and ?cpcG1 included) grown under (A) 10 ?mol m–2 s–1 for 5 or 7 days or (B) 80 ?mol m–2 s–1 for 5 days of white light in BG-11/HEPES medium. 2.5 ?g of proteins were resolved on 10% (w/v) polyacrylamide gels by SDS-PAGE electrophoresis prior to immunoblotting. Arrowheads indicated OCP or RbcL proteins.


Reactant: Synechocystis

Application: Western Blotting

Pudmed ID: 31143173

Journal: Front Microbiol

Figure Number: 7B

Published Date: 2019-05-31

First Author: Oh, S. & Montgomery, B. L.

Impact Factor: 5.259

Open Publication

Accumulation of OCP protein in WT and phycobilisome-deficient strains. Immunoblot analysis was performed using anti-OCP antibody (top panels) or anti-RbcL antibody (bottom panels), with representative blots shown. Total soluble proteins were extracted from wild-type (WT), ?cpcF and ?cpcG1 strains (two independent mutant strains for each ?cpcF and ?cpcG1 included) grown under (A) 10 ?mol m–2 s–1 for 5 or 7 days or (B) 80 ?mol m–2 s–1 for 5 days of white light in BG-11/HEPES medium. 2.5 ?g of proteins were resolved on 10% (w/v) polyacrylamide gels by SDS-PAGE electrophoresis prior to immunoblotting. Arrowheads indicated OCP or RbcL proteins.

Additional information

RbcS subunit is not detected by this antibody

This product can be sold containing proclin if requested

Related products

Background

Background

Rubisco (Ribulose-1,5-bisphosphate carboxylase/oxygenase) catalyzes the rate-limiting step of CO2 fixation in photosynthetic organisms. It is demonstrably homologous from purple bacteria to flowering plants and consists of two protein subunits, each present in 8 copies. In plants and green algae, the large subunit (~55 kDa) is coded by the chloroplast rbcL gene, and the small subunit (15 kDa) is coded by a family of nuclear rbcS genes.

Product citations

Selected references Mihara et al. (2019). Thioredoxin targets are regulated in heterocysts of cyanobacterium Anabaena sp. PCC 7120 in a light-independent manner. J Exp Bot. 2019 Dec 21. pii: erz561. doi: 10.1093/jxb/erz561.
Sedaghatmehr et al. (2019). A regulatory role of autophagy for resetting the memory of heat stress in plants. Plant Cell Environ. 2019 Mar;42(3):1054-1064. doi: 10.1111/pce.13426.
Rohnke et al. (2018). RcaE-Dependent Regulation of Carboxysome Structural Proteins Has a Central Role in Environmental Determination of Carboxysome Morphology and Abundance in Fremyella diplosiphon. Mol Biol and Physiol. Vol. 3, Issue 1. DOI: 10.1128/mSphere.00617-17
Zhang et al. (2017). Composition of photosynthetic pigments and photosynthetic characteristics in green and yellow sectors of the variegated Aucuba japonica ‘Variegata’ leaves. Flora, Vol 240, March 2018, Pages 25–33.
Wang et al. (2017). Re-creation of a Key Step in the Evolutionary Switch from C3 to C4 Leaf Anatomy. Curr Biol. 2017 Nov 6;27(21):3278-3287.e6. doi: 10.1016/j.cub.2017.09.040.
Wen and Zhang (2014). Salsola laricifolia, another C 3 –C 4 intermediate species in tribe Salsoleae s.l. (Chenopodiaceae). Photosynth Res. 2014 Sep 17. (immunolocalization)
Feifei et al. (2014). Comparison of Leaf Proteomes of Cassava (Manihot esculenta Crantz) Cultivar NZ199 Diploid and Autotetraploid Genotypes. PLoS One. 2014 Apr 11;9(4):e85991. doi: 10.1371/journal.pone.0085991. eCollection 2014.
immunogen:

purified 557 kDa hexadecamer Rubisco protein complex from Spinacia oleracea (SIGMA-ALDRICH R-8000), UniProt: P00875 and Q43832

Reconstitution: For reconstitution add 50 ĩl of sterile water
Host: Rabbit
Clonality: Polyclonal
Purity: Serum
Format: Lyophilized
Quantity: 50 ĩl
storage: Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.
tested applications: Immunolocalization (IL), Western blot (WB)
recommended dilution: 1 : 10 000-1 : 20 000 on 0,5-10 ug total cellular protein/lane and standard (WB), 1 : 500-1:1000 (IL)
calculated | apparent molecular mass [kDa]:

53-55 | 53-55 kDa

Confirmed reactivity: Anabaena sp. PCC 7120, Arabidopsis thaliana, Aucuba japonica, Fremyella diplosiphon, Glycine max, Hordeum vulgare, Manihot esculenta Crantz, Oryza sativa, Physcomitrium patens, Pisum sativum, Populus sp., Salsola laricifolia, Solanum tuberosum, Spinacia oleracea, Synechocystis sp. PCC 6803, Synechococcus sp. PCC7942, Zea mays
predicted reactivity: higher plants, algae, Nannochloropsis sp.
not reactive in: Chlamydomonas reinhardtii (immulolocalization)
Picture (footer): Application example

0.5 µg of total leaf protein isolated with Agrisera Protein Eextraction Buffer (AS08 300) from Arabidopsis thaliana (1), Spinacia oleracea (2), Zea mays (3), Hordeum vulgare (4), Solanum tuberosum (5), Pisum sativum (6) were separated on 4-12% NuPage (Invitrogen) LDS-PAGE and blotted 45 min (30V) to nitrocellulose.  Filters where blocked 1h with 2% low-fat milk powder in TBS-T (0.1% TWEEN 20) and probed with AS07 218 (1:20 000, 1h) and secondary anti-rabbit (1:20000, 1 h) antibody (HRP conjugated) 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 chemiluminescence using a Fuji LAS-3000 CCD (300s, high sensitivity).

More images:

Reactant: Manihot esculenta (Cassava)

Application: Western Blotting

Pudmed ID: 20187967

Journal: Proteome Sci

Figure Number: 5A

Published Date: 2010-02-27

First Author: Li, K., Zhu, W., et al.

Impact Factor: 2.037

Open Publication

Western blotting of Rubisco and ?-tubulan. Rubisco and ?-tubulan in the somatic embryos, plantlets and tuberous roots of cassava cultivar SC8 were detected by Western blotting using antiRubisco-polyclonal antibody from Agrisera (AS07218) and anti-?-tubulin-monoclonal antibody from Sigma-Aldrich (T9026). ARs, adventitious roots.


Reactant: Manihot esculenta (Cassava)

Application: Western Blotting

Pudmed ID: 24727655

Journal: PLoS One

Figure Number: 5A

Published Date: 2014-04-15

First Author: An, F., Fan, J., et al.

Impact Factor: 2.942

Open Publication

Western blotting of Rubisco, APX and PrxQ.The expression of Rubisco, APX and PrxQ in leaves of cassava NZ199 diploid (a) and autotetraploid (b) genotypes were detected by western blotting using antiRubisco-polyclonal antibody (AS07218), anti-APX antibody (AS08368) and anti-PrxQ antibody (AS05093) from Agrisera, respectively.


Reactant: Manihot esculenta (Cassava)

Application: Western Blotting

Pudmed ID: 27881899

Journal: Plant Mol Biol Report

Figure Number: 8A

Published Date: 2016-11-25

First Author: An, F., Li, G., et al.

Impact Factor: 1.526

Open Publication

Western blotting of Rubisco and peroxiredoxin. The expressions of Rubisco (a) and peroxiredoxin (b) in apical expanded leaves of SC8and Col1046 were detected by Western blotting using anti-Rubisco polyclonal antibody (AS07218) and anti-peroxiredoxin antibody (AS05093) from Agrisera, respectively. Mr, protein marker; lines a and b, the expression of Rubisco and peroxiredoxin of SC8 in 5 °C for 0 and 10 days, respectively; lines c and d, the expression of Rubisco and peroxiredoxin of Co11046 in 5 °C for 0 and 10 days, respectively


Reactant: Synechocystis

Application: Western Blotting

Pudmed ID: 31143173

Journal: Front Microbiol

Figure Number: 7A

Published Date: 2019-05-31

First Author: Oh, S. & Montgomery, B. L.

Impact Factor: 5.259

Open Publication

Accumulation of OCP protein in WT and phycobilisome-deficient strains. Immunoblot analysis was performed using anti-OCP antibody (top panels) or anti-RbcL antibody (bottom panels), with representative blots shown. Total soluble proteins were extracted from wild-type (WT), ?cpcF and ?cpcG1 strains (two independent mutant strains for each ?cpcF and ?cpcG1 included) grown under (A) 10 ?mol m–2 s–1 for 5 or 7 days or (B) 80 ?mol m–2 s–1 for 5 days of white light in BG-11/HEPES medium. 2.5 ?g of proteins were resolved on 10% (w/v) polyacrylamide gels by SDS-PAGE electrophoresis prior to immunoblotting. Arrowheads indicated OCP or RbcL proteins.


Reactant: Synechocystis

Application: Western Blotting

Pudmed ID: 31143173

Journal: Front Microbiol

Figure Number: 7B

Published Date: 2019-05-31

First Author: Oh, S. & Montgomery, B. L.

Impact Factor: 5.259

Open Publication

Accumulation of OCP protein in WT and phycobilisome-deficient strains. Immunoblot analysis was performed using anti-OCP antibody (top panels) or anti-RbcL antibody (bottom panels), with representative blots shown. Total soluble proteins were extracted from wild-type (WT), ?cpcF and ?cpcG1 strains (two independent mutant strains for each ?cpcF and ?cpcG1 included) grown under (A) 10 ?mol m–2 s–1 for 5 or 7 days or (B) 80 ?mol m–2 s–1 for 5 days of white light in BG-11/HEPES medium. 2.5 ?g of proteins were resolved on 10% (w/v) polyacrylamide gels by SDS-PAGE electrophoresis prior to immunoblotting. Arrowheads indicated OCP or RbcL proteins.

additional information (application):

RbcS subunit is not detected by this antibody

This product can be sold containing proclin if requested

background:

Rubisco (Ribulose-1,5-bisphosphate carboxylase/oxygenase) catalyzes the rate-limiting step of CO2 fixation in photosynthetic organisms. It is demonstrably homologous from purple bacteria to flowering plants and consists of two protein subunits, each present in 8 copies. In plants and green algae, the large subunit (~55 kDa) is coded by the chloroplast rbcL gene, and the small subunit (15 kDa) is coded by a family of nuclear rbcS genes.

All references: Mihara et al. (2019). Thioredoxin targets are regulated in heterocysts of cyanobacterium Anabaena sp. PCC 7120 in a light-independent manner. J Exp Bot. 2019 Dec 21. pii: erz561. doi: 10.1093/jxb/erz561.
Sedaghatmehr et al. (2019). A regulatory role of autophagy for resetting the memory of heat stress in plants. Plant Cell Environ. 2019 Mar;42(3):1054-1064. doi: 10.1111/pce.13426.
Rohnke et al. (2018). RcaE-Dependent Regulation of Carboxysome Structural Proteins Has a Central Role in Environmental Determination of Carboxysome Morphology and Abundance in Fremyella diplosiphon. Mol Biol and Physiol. Vol. 3, Issue 1. DOI: 10.1128/mSphere.00617-17
Zhang et al. (2017). Composition of photosynthetic pigments and photosynthetic characteristics in green and yellow sectors of the variegated Aucuba japonica ‘Variegata’ leaves. Flora, Vol 240, March 2018, Pages 25–33.
Wang et al. (2017). Re-creation of a Key Step in the Evolutionary Switch from C3 to C4 Leaf Anatomy. Curr Biol. 2017 Nov 6;27(21):3278-3287.e6. doi: 10.1016/j.cub.2017.09.040.
Wen and Zhang (2014). Salsola laricifolia, another C 3 –C 4 intermediate species in tribe Salsoleae s.l. (Chenopodiaceae). Photosynth Res. 2014 Sep 17. (immunolocalization)
Feifei et al. (2014). Comparison of Leaf Proteomes of Cassava (Manihot esculenta Crantz) Cultivar NZ199 Diploid and Autotetraploid Genotypes. PLoS One. 2014 Apr 11;9(4):e85991. doi: 10.1371/journal.pone.0085991. eCollection 2014.

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