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PHOT2 | Phototropin-2

AS10 721 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Arabidopsis thaliana

PHOT2 | Phototropin-2 in the group Antibodies Plant/Algal  / Plant Developmental Biology / Photomorphogenesis at Agrisera AB (Antibodies for research) (AS10 721)
PHOT2 | Phototropin-2



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Data sheet Product citations Protocols Add review

Product Information

Immunogen

KLH-conjugated synthetic peptide derived from known Arabidopsis thaliana PHOT2 P93025, At5g58140

Host Rabbit
Clonality Polyclonal
Purity Serum
Format Lyophilized
Quantity 50 µl
Reconstitution 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 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 : 10 000 (WB)
Expected | apparent MW

102 | 110 kDa

Reactivity

Confirmed reactivity Arabidopsis thaliana
Predicted reactivity Arabidopsis thaliana
Not reactive in

Oryza sativa

Application examples

Application examples

application example

80 µg of total protein from Arabidopsis thaliana wt Columbia (right lane) and Arabidopsis thaliana phot1phot2 double mutant (left lane) were separated on 9% SDS-PAGE and blotted 2h to PVDF. Blots were blocked immediately following transfer in PBS-T 5% milk for 1h at room temperature with agitation. Blots were incubated in the primary antibody at a dilution of 1: 10 000 overnight at 4oC with agitation. The antibody solution was decanted and the blot was rinsed briefly, then washed 3 times for 5 min in PBS-T at room temperature with agitation. Blots were incubated in secondary antibody (goat anti- rabbit IgG horse radish peroxidase conjugated, from Agrisera AS09 602) diluted to 1:10 000 for 1h at room temperature with agitation. The blots were washed as above and developed with WestPico detection reagent (PIERCE) according to the manufacturers instructions. Exposure time was 300 seconds.

 


western blot using anti-AtPHOT2 antibodies

Reactant: Arabidopsis thaliana (Thale cress)

Application: Western Blotting

Pudmed ID: 27406783

Journal: J Exp Bot

Figure Number: 6D

Published Date: 2016-09-01

First Author: Sztatelman, O., ?abuz, J., et al.

Impact Factor: 6.088

Open Publication

Profiles of phototropin1 (A) and phototropin2 (B) expression in darkened and light-exposed (120 µmol m?2 s?1 and 3h) Arabidopsis wild-type and mutant (phot1, phot2, and rcn1) leaves at the mRNA level. Each point represents the average obtained from at least nine leaves of different plants. Error bars show the SE. Asterisks indicate statistically significant differences between samples *P=0.01–0.05. (C and D) A representative western blot showing the expression of PHOT1 (C) and PHOT2 (D) in wild-type and mutant plants. Proteins stained with CBB are shown as the well loading reference.


Reactant: Arabidopsis thaliana (Thale cress)

Application: Western Blotting

Pudmed ID: 27406783

Journal: J Exp Bot

Figure Number: 7A

Published Date: 2016-09-01

First Author: Sztatelman, O., ?abuz, J., et al.

Impact Factor: 6.088

Open Publication

Representative dephosphorylation profiles of phototropin1 after blue light exposure (120 µmol m?2 s?1 and 1h) in Arabidopsis wild-type and mutant (phot2 and rcn1) leaves. Dark, a dark-adapted control; 0, a sample collected just after illumination. The duration of the incubation in the darkness after the end of the illumination is indicated in minutes. Phosphorylation leads to the shift of the phototropin band towards higher mass. Samples treated with alkaline phosphatase are shown on the right. Anti-actin blots are presented as the loading reference. The results represent two out of 4–5 independent biological replicates.


Reactant: Arabidopsis thaliana (Thale cress)

Application: Western Blotting

Pudmed ID: 27406783

Journal: J Exp Bot

Figure Number: 8A

Published Date: 2016-09-01

First Author: Sztatelman, O., ?abuz, J., et al.

Impact Factor: 6.088

Open Publication

Representative dephosphorylation profiles of phototropin2 after blue light exposure (120 µmol m?2 s?1 and 1h) in Arabidopsis wild-type and mutant (phot1 and rcn1) leaves. For further description, see the legend of Fig. 7. The results represent one of 3–4 independent biological replicates.

Additional information

Additional information This product can be sold containing ProClin if requested

Related products

Background

Background

PHOT2 | phototropin-2 is a membrane-bound serine/threonine kinase that functions as blue light photoreceptor in redundancy with PHOT1. Involved in processed like stomatal opening, chloroplast movement and phototropism. Alternative names: NPL1, K21L19.6, AtKin7, Defective in chloroplast avoidance protein 1
Non-phototropic hypocotyl 1-like protein 1, NPH1-like protein 1.

Product citations

Selected references Labuz et al. (2021) Phototropin interactions with SUMO proteins. Plant Cell Physiol. 2021 Feb 17:pcab027. doi: 10.1093/pcp/pcab027. Epub ahead of print. PMID: 33594440.
Krzeszowiec et al. (2020). Chloroplasts in C3 grasses move in response to blue-light. Plant Cell Rep . 2020 Oct;39(10):1331-1343.doi: 10.1007/s00299-020-02567-3. Epub 2020 Jul 13.
Labuz et al. (2015). The impact of temperature on blue light induced chloroplast movements in Arabidopsis thaliana. Plant Science, doi:10.1016/j.plantsci.2015.07.013.
Aggarwal et al. (2014). Blue-light-activated phototropin2 trafficking from the cytoplasm to Golgi/post-Golgi vesicles. J Exp Bot. 2014 May 12.
immunogen:

KLH-conjugated synthetic peptide derived from known Arabidopsis thaliana PHOT2 P93025, At5g58140

Reconstitution: For reconstitution add 100 µl of sterile water
Host: Rabbit
Clonality: Polyclonal
Purity: Serum
Format: Lyophilized
Quantity: 50 µl
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 : 10 000 (WB)
calculated | apparent molecular mass [kDa]:

102 | 110 kDa

Confirmed reactivity: Arabidopsis thaliana
predicted reactivity: Arabidopsis thaliana
not reactive in:

Oryza sativa

Picture (footer):

application example

80 µg of total protein from Arabidopsis thaliana wt Columbia (right lane) and Arabidopsis thaliana phot1phot2 double mutant (left lane) were separated on 9% SDS-PAGE and blotted 2h to PVDF. Blots were blocked immediately following transfer in PBS-T 5% milk for 1h at room temperature with agitation. Blots were incubated in the primary antibody at a dilution of 1: 10 000 overnight at 4oC with agitation. The antibody solution was decanted and the blot was rinsed briefly, then washed 3 times for 5 min in PBS-T at room temperature with agitation. Blots were incubated in secondary antibody (goat anti- rabbit IgG horse radish peroxidase conjugated, from Agrisera AS09 602) diluted to 1:10 000 for 1h at room temperature with agitation. The blots were washed as above and developed with WestPico detection reagent (PIERCE) according to the manufacturers instructions. Exposure time was 300 seconds.

 


western blot using anti-AtPHOT2 antibodies
More images:

Reactant: Arabidopsis thaliana (Thale cress)

Application: Western Blotting

Pudmed ID: 27406783

Journal: J Exp Bot

Figure Number: 6D

Published Date: 2016-09-01

First Author: Sztatelman, O., ?abuz, J., et al.

Impact Factor: 6.088

Open Publication

Profiles of phototropin1 (A) and phototropin2 (B) expression in darkened and light-exposed (120 µmol m?2 s?1 and 3h) Arabidopsis wild-type and mutant (phot1, phot2, and rcn1) leaves at the mRNA level. Each point represents the average obtained from at least nine leaves of different plants. Error bars show the SE. Asterisks indicate statistically significant differences between samples *P=0.01–0.05. (C and D) A representative western blot showing the expression of PHOT1 (C) and PHOT2 (D) in wild-type and mutant plants. Proteins stained with CBB are shown as the well loading reference.


Reactant: Arabidopsis thaliana (Thale cress)

Application: Western Blotting

Pudmed ID: 27406783

Journal: J Exp Bot

Figure Number: 7A

Published Date: 2016-09-01

First Author: Sztatelman, O., ?abuz, J., et al.

Impact Factor: 6.088

Open Publication

Representative dephosphorylation profiles of phototropin1 after blue light exposure (120 µmol m?2 s?1 and 1h) in Arabidopsis wild-type and mutant (phot2 and rcn1) leaves. Dark, a dark-adapted control; 0, a sample collected just after illumination. The duration of the incubation in the darkness after the end of the illumination is indicated in minutes. Phosphorylation leads to the shift of the phototropin band towards higher mass. Samples treated with alkaline phosphatase are shown on the right. Anti-actin blots are presented as the loading reference. The results represent two out of 4–5 independent biological replicates.


Reactant: Arabidopsis thaliana (Thale cress)

Application: Western Blotting

Pudmed ID: 27406783

Journal: J Exp Bot

Figure Number: 8A

Published Date: 2016-09-01

First Author: Sztatelman, O., ?abuz, J., et al.

Impact Factor: 6.088

Open Publication

Representative dephosphorylation profiles of phototropin2 after blue light exposure (120 µmol m?2 s?1 and 1h) in Arabidopsis wild-type and mutant (phot1 and rcn1) leaves. For further description, see the legend of Fig. 7. The results represent one of 3–4 independent biological replicates.

additional information: This product can be sold containing ProClin if requested
background:

PHOT2 | phototropin-2 is a membrane-bound serine/threonine kinase that functions as blue light photoreceptor in redundancy with PHOT1. Involved in processed like stomatal opening, chloroplast movement and phototropism. Alternative names: NPL1, K21L19.6, AtKin7, Defective in chloroplast avoidance protein 1
Non-phototropic hypocotyl 1-like protein 1, NPH1-like protein 1.

All references: Labuz et al. (2021) Phototropin interactions with SUMO proteins. Plant Cell Physiol. 2021 Feb 17:pcab027. doi: 10.1093/pcp/pcab027. Epub ahead of print. PMID: 33594440.
Krzeszowiec et al. (2020). Chloroplasts in C3 grasses move in response to blue-light. Plant Cell Rep . 2020 Oct;39(10):1331-1343.doi: 10.1007/s00299-020-02567-3. Epub 2020 Jul 13.
Labuz et al. (2015). The impact of temperature on blue light induced chloroplast movements in Arabidopsis thaliana. Plant Science, doi:10.1016/j.plantsci.2015.07.013.
Aggarwal et al. (2014). Blue-light-activated phototropin2 trafficking from the cytoplasm to Golgi/post-Golgi vesicles. J Exp Bot. 2014 May 12.

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