14-3-3 GRF | General regulatory element
AS12 2119 | Clonality: Polyclonal | Host: Rabbit | Reactivity: A. platanoides, A. thaliana, L. longiflorum. M. crystallinum, N. tabacum, O. sativa, P. vulgaris, algae N. oloabundans
|Recommended dilution||1: 2000 (WB)|
|Expected | apparent MW||
20-28 kDa (depending upon an isoform)
|Confirmed reactivity||Aesculus hippocastanum, Arabidopsis halleri, Arabidopsis thaliana, Lilium longiflorum, Mesembryanthemum crystallinum, Neochloris oloabundans (algae), Oryza sativa, Phaseolus vulgaris, Vicia faba
Brassica sp., Chlamydomonas reinhardtii, Gossypium hirsutum, Nicotiana tabacum, Physcomitrella patens, Pisum sativum, Solanum tuberosum, Triticum aestivum, Zea mays
|Not reactive in||
This antibody does not bind to 14-3-3-like protein D of Nicotiana tabacum.
This product can be sold containing proclin if requested.
|Selected references||Obroucheva (2017). Participation of Plasma Membrane H+-ATPase in Seed Germination. Internat. J. of Cell Science & Molecular Biol. Vol. 2 Issue 3. DOI : 10.19080/IJCSMB.2017.02.555589.
Barkla et al. (2016). Single-cell-type quantitative proteomic and ionomic analysis of epidermal bladder cells from the halophyte model plant Mesembryanthemum crystallinum to identify salt-responsive proteins. BMC Plant Biol. 2016 May 10;16(1):110. doi: 10.1186/s12870-016-0797-1.
Left panel: 150 ng of recombinant Arabidopsis thaliana, Physcomitrella patens and Chlamydomonas reinhardtii GRFs (see more details below) were separated on 12 % SDS-PAGE and blotted 1h to PVDF by semi dry blotting (0.8 mA/cm2 for 60 min). Blots were blocked with 2% skimmed milk powder dissolved in TBST (0.1 % Tween 20) for 1h at room temperature (RT) with agitation. Blot was incubated in the primary antibody at a dilution of 1: 1 000 in blocking solution and incubated for 1h at RT 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 secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated, from Agrisera AS09 602) diluted to 1:20 000 in for 1h at RT with agitation. The blot was washed as above and developed for 5 min with ECL Prime western blotting detection reagent according to the manufacturer's instructions (GE Healthcare, #RPN2232). Exposure time was 10 minutes.
Right panel: 50 µg of a total cell extract of Arabidopsis thaliana wilde type. Conditions as above, exposure time 30 seconds.
GRF protein designations: At 14-3-3 lambda (GRF6), At 14-3-3 chi (GRF1), At14-3-3 psi (GRF3), At14-3-3 omega (GRF2), At14-3-3 upsilon (GRF5), At14-3-3 omicron (GRF11), At14-3-3 kappa (GRF8), Pp 14-3-3 Pp1s 73_133V6 (closest homolog to At GRF6), Cr 14-3-3 Cre 12.g559250 (closest homolog to AtGRF6). Note that all recombinant GRFs were detected by this antibody, At14-3-3 kappa (GRF8) to a lesser extent.
Courtesy of Dr. Bernhard Wurzinger, University of Vienna, Austria
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