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STT7 | Serine/threonine-protein kinase STT7 (chloroplastic)

AS15 3080 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Chlamydomonas reinhardtii
STT7 | Serine/threonine-protein kinase STT7 (chloroplastic)  in the group Antibodies Plant/Algal  / Photosynthesis  / Kinases at Agrisera AB (Antibodies for research) (AS15 3080)
STT7 | Serine/threonine-protein kinase STT7 (chloroplastic)



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Product Information

Immunogen Recombinant STT7 of Chlamydomonas reinhardtii, overexpressed in E.coli, UniProt: Q84V18
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 Western blot (WB)
Recommended dilution 1 : 1000-1 : 2 500 (WB)
Expected | apparent MW 80,7 | 80 kDa

Reactivity

Confirmed reactivity Chlamydomonas reinhardtii
Predicted reactivity Chlamydomonas reinhardtii
Not reactive in No confirmed exceptions from predicted reactivity are currently known

Application examples

Application examples Application example

Western blot using anti-STT7 antibodies

Total cells of Chlamydomonas reinhardtii were kept under state I (no expression of LHCII kinase, line 1) and state II (expression of LHCII kinase, line 2). 2 µg of chlorophyll content were solubilised in buffer containing 120 mM Tris (6.8) 4% SDS, 20% glycerol and 1 mM DTT and denatured with at 100°C for 1 min (Takahashi et al., 2013) were separated on 12 % SDS-PAGE and blotted 20 min to nitrocellulose using semi-dry transfer. Blot was blocked with 4% milk RT/2h with agitation. Blot was incubated in the primary antibody at a dilution of 1: 3000 for TBS-T ON/4°C 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 RT with agitation. Blot was incubated in Agrisera matching secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, AS09 602) diluted to 1:25 000 in for 1h/RT with agitation. The blot was washed as above and developed for 30 sec with ECL. Exposure time was 30 to 60 seconds. The molecular weight of the identified band is approx. 80 KD.

Courtesy Dr. Sai Kiran, University of Hyderbad, India

Additional information

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Background

Background Serine/threonine-protein kinase stt7, chloroplastic is required for state transition by phosphorylating light-harvesting complex II outer antennae (LCHII).

Product citations

Selected references Cazzaniga et al. (2019). Photosystem II antenna complexes CP26 and CP29 are essential for non�photochemical quenching in Chlamydomonas reinhardtii. doi: 10.1111/pce.13680.
Upadhyaya and Jagadeeshwar Rao (2019). Reciprocal regulation of photosynthesis and mitochondrial respiration by TOR kinase in Chlamydomonas reinhardtii. Plant Direct Volume 3, Issue 11.
Lameille et al. (2009). Analysis of the chloroplast protein kinase Stt7 during state transitions. PLoS Biol. 2009 Mar 3;7(3):e45. doi: 10.1371/journal.pbio.1000045.
All references: Cazzaniga et al. (2019). Photosystem II antenna complexes CP26 and CP29 are essential for non�photochemical quenching in Chlamydomonas reinhardtii. doi: 10.1111/pce.13680.
Upadhyaya and Jagadeeshwar Rao (2019). Reciprocal regulation of photosynthesis and mitochondrial respiration by TOR kinase in Chlamydomonas reinhardtii. Plant Direct Volume 3, Issue 11.
Lameille et al. (2009). Analysis of the chloroplast protein kinase Stt7 during state transitions. PLoS Biol. 2009 Mar 3;7(3):e45. doi: 10.1371/journal.pbio.1000045.
Picture (footer): Application example

Western blot using anti-STT7 antibodies

Total cells of Chlamydomonas reinhardtii were kept under state I (no expression of LHCII kinase, line 1) and state II (expression of LHCII kinase, line 2). 2 µg of chlorophyll content were solubilised in buffer containing 120 mM Tris (6.8) 4% SDS, 20% glycerol and 1 mM DTT and denatured with at 100°C for 1 min (Takahashi et al., 2013) were separated on 12 % SDS-PAGE and blotted 20 min to nitrocellulose using semi-dry transfer. Blot was blocked with 4% milk RT/2h with agitation. Blot was incubated in the primary antibody at a dilution of 1: 3000 for TBS-T ON/4°C 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 RT with agitation. Blot was incubated in Agrisera matching secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, AS09 602) diluted to 1:25 000 in for 1h/RT with agitation. The blot was washed as above and developed for 30 sec with ECL. Exposure time was 30 to 60 seconds. The molecular weight of the identified band is approx. 80 KD.

Courtesy Dr. Sai Kiran, University of Hyderbad, India
background: Serine/threonine-protein kinase stt7, chloroplastic is required for state transition by phosphorylating light-harvesting complex II outer antennae (LCHII).
Confirmed reactivity: Chlamydomonas reinhardtii
predicted reactivity: Chlamydomonas reinhardtii
not reactive in: No confirmed exceptions from predicted reactivity are currently known
calculated | apparent molecular mass [kDa]: 80,7 | 80 kDa
Clonality: Polyclonal
Format: Lyophilized
Host: Rabbit
immunogen: Recombinant STT7 of Chlamydomonas reinhardtii, overexpressed in E.coli, UniProt: Q84V18
Purity: Serum
Quantity: 50 ĩl
recommended dilution: 1 : 1000-1 : 2 500 (WB)
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: Western blot (WB)

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