KUA1 | MYB transcription factor

Name: KUA1 | MYB transcription factor
SKU: AS15 2989
Price: 302 EUR
Availability: InStock

AS15 2989 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Arabidopsis thaliana

KUA1 | MYB transcription factor in the group Antibodies Plant/Algal / DNA/RNA/Cell Cycle / Transcription regulation at Agrisera AB (Antibodies for research) (AS15 2989)

Product Information

Immunogen

KLH-conjugated peptide derived from Arabidopsis thaliana KUA1 protein sequence, UniProt: Q9LVS0,
TAIR:AT5G47390 .The peptide used to elicit this antibody is also conserved in MYB1R1 of Triticum urartu UniProt:M7YW99 and MYBS3 of Oryza sativa subsp. japonica, UniProt: Q7XC57-2

Host Rabbit

Clonality Polyclonal

Purity Serum

Format Lyophilized

Quantity 50 µl

Reconstitution For reconstitution add 50 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 : 5000 (WB)

Expected | apparent MW 39,6 kDa

Reactivity

Confirmed reactivity Arabidopsis thaliana, Beta vulgaris

Predicted reactivity Capsicum annuum, Cephalotus follicularis, Cicer arietinum, Glycine max, Glycine soja, Gossypium arboretum, Cucumis melo, Medicago truncatula, Nelumbo nucifera, Nicotiana tabacum, Nicotiana sylvestris, Theobroma cacao, Vigna radiata var. radiata
Species of your interest not listed? Contact us

Not reactive in No confirmed exceptions from predicted reactivity are currently known

Application examples

Application example

10-20 µg of total protein from fresh Arabidopsis thaliana leaves was grinded and extracted in 10 mM Tris/HCL pH 7,5; 50 mM NaCl; 0,5 mM EDTA, 1% Triton X-100 supplemented with protease inhibitor cocktail (Sigma, P9599). After 15 minutes of incubation on ice the extracts were centrifuged at 6000g for 5 minutes at 4 degrees. The supernatant was mixed with 2X Laemli buffer and denatured at 96°C for 5 min. After cooling down, the samples were separated on 12 % SDS-PAGE gel and blotted to PVDF in 9 minutes using a Pierce G2 Fast Blotter in transfer buffer. Blots were blocked with 5% blocking solution (containing non-fat milk protein in TBS) for 1h at room temperature (RT) with agitation. Blot was incubated in the primary antibody at a dilution of 1: 5000 overnight in 5% blocking solution. The antibody solution was decanted and the blot was rinsed briefly twice, then washed twice for 10 min with TBS-T and twice for 10 min in 5% blocking solution at RT with agitation. Blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Agrisera AS09 602) diluted to 1:10 000 in 5% blocking solution for 90 minutes at RT with agitation. The blot was washed four times in TBS-T for 10 minutes as described above and developed using chemiluminescent detection reagent. Blots were imaged using a BioRad Chemidoc system using an exposure time of 300 seconds.

Courtesy Dr. Jozefus Schippers, University of Aachen, Germany

Additional information

The antibody was used in tissue printing on German sugar beet and was found in vascular bundles

Background

Background KUA1 (MYB transcription factor) involved in regulation of hypocotyl elongation in response to darkness by enhancing auxin accumulation in a phytochrome-interacting factor (PIF) proteins-dependent manner. Promotes lateral roots formation and place a critical role in in developmentally regulated and dark-induced onset of leaf senescence by repressing the transcription of several genes involved in chloroplast function and responses to light and auxin. Promotes responses to auxin, abscisic acid (ABA), and ethylene. Alternative names: Myb-related protein H, AtMYBH, AtMYBS3, MYBS3-homolg protein, Protein KUODA1.

Product citations

Selected references Pandey et al. (2019). Epigenetic control of UV-B-induced flavonoid accumulation in Artemisia annua L. Planta. 2019 Feb;249(2):497-514. doi: 10.1007/s00425-018-3022-7.

Confirmed reactivity:	Arabidopsis thaliana, Beta vulgaris
predicted reactivity:	Capsicum annuum, Cephalotus follicularis, Cicer arietinum, Glycine max, Glycine soja, Gossypium arboretum, Cucumis melo, Medicago truncatula, Nelumbo nucifera, Nicotiana tabacum, Nicotiana sylvestris, Theobroma cacao, Vigna radiata var. radiata Species of your interest not listed? Contact us
not reactive in:	No confirmed exceptions from predicted reactivity are currently known
Picture (footer):	Application example 10-20 µg of total protein from fresh Arabidopsis thaliana leaves was grinded and extracted in 10 mM Tris/HCL pH 7,5; 50 mM NaCl; 0,5 mM EDTA, 1% Triton X-100 supplemented with protease inhibitor cocktail (Sigma, P9599). After 15 minutes of incubation on ice the extracts were centrifuged at 6000g for 5 minutes at 4 degrees. The supernatant was mixed with 2X Laemli buffer and denatured at 96°C for 5 min. After cooling down, the samples were separated on 12 % SDS-PAGE gel and blotted to PVDF in 9 minutes using a Pierce G2 Fast Blotter in transfer buffer. Blots were blocked with 5% blocking solution (containing non-fat milk protein in TBS) for 1h at room temperature (RT) with agitation. Blot was incubated in the primary antibody at a dilution of 1: 5000 overnight in 5% blocking solution. The antibody solution was decanted and the blot was rinsed briefly twice, then washed twice for 10 min with TBS-T and twice for 10 min in 5% blocking solution at RT with agitation. Blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Agrisera AS09 602) diluted to 1:10 000 in 5% blocking solution for 90 minutes at RT with agitation. The blot was washed four times in TBS-T for 10 minutes as described above and developed using chemiluminescent detection reagent. Blots were imaged using a BioRad Chemidoc system using an exposure time of 300 seconds. Courtesy Dr. Jozefus Schippers, University of Aachen, Germany
calculated \| apparent molecular mass [kDa]:	39,6 kDa
Clonality:	Polyclonal
Format:	Lyophilized
Host:	Rabbit
immunogen:	KLH-conjugated peptide derived from Arabidopsis thaliana KUA1 protein sequence, UniProt: Q9LVS0, TAIR:AT5G47390 .The peptide used to elicit this antibody is also conserved in MYB1R1 of Triticum urartu UniProt:M7YW99 and MYBS3 of Oryza sativa subsp. japonica, UniProt: Q7XC57-2
Purity:	Serum
Quantity:	50 µl
recommended dilution:	1 : 5000 (WB)
Reconstitution:	For reconstitution add 50 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)
additional information (application):	The antibody was used in tissue printing on German sugar beet and was found in vascular bundles
All references:	Pandey et al. (2019). Epigenetic control of UV-B-induced flavonoid accumulation in Artemisia annua L. Planta. 2019 Feb;249(2):497-514. doi: 10.1007/s00425-018-3022-7.
background:	KUA1 (MYB transcription factor) involved in regulation of hypocotyl elongation in response to darkness by enhancing auxin accumulation in a phytochrome-interacting factor (PIF) proteins-dependent manner. Promotes lateral roots formation and place a critical role in in developmentally regulated and dark-induced onset of leaf senescence by repressing the transcription of several genes involved in chloroplast function and responses to light and auxin. Promotes responses to auxin, abscisic acid (ABA), and ethylene. Alternative names: Myb-related protein H, AtMYBH, AtMYBS3, MYBS3-homolg protein, Protein KUODA1.

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