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application information | ||
recommended dilution | 1:10 000 with standard ECL (WB), 2 µg (IP), 1: 500 (IL) | |
expected | apparent MW | 28 kDa | |
confirmed reactivity | Arabidopsis thaliana (immunohistochemistry only) D. salina, A. toxicaria, Horderum vulgare, Pisum sativum, Silene vulgaris, S. lycopersicum, , Solanum tuberosum, P. silvestris, Zea mays | |
predicted reactivity | dicots including: Brassica. juncea, Fragaria ananassa, Gossypium hirsutum, Nicotiana tabacum,, Solanum tuberosum, Vitis vinifera, monocots including: Oryza sativa, trees: Pinus pinaster | |
not reactive in | no confirmed exceptions from predicted reactivity known in the moment | |
additional information | ||
selected references | Tsaniklidis et al. (2013). L-Ascorbic acid metabolism in parthenocarpic and seeded cherry tomatoes. Plant Growth Regul,DOI 10.1007/s10725-013-9845-0. (Solanum lycopersicum, immunolocalization) Correa-Aragunde et al. (2013). Auxin induces redox regulation of ascorbate peroxidase 1 activity by S-nitrosylation/denitrosylation balance resulting in changes of root growth pattern in Arabidopsis. J Exp Bot, Aug;64(11):3339-49. Wu et al. (2013). Comparative proteomic analysis of the plant-virus interaction in resistant and susceptible ecotypes of maize infected with sugarcane mosaic virus. J. Proteomics, June 14th. Sobrino-Plata et al. (2013). Specific stress responses to cadmium, arsenic and mercury appear in the |
application example (A) , (B)- control antibody, anti-PIN1, (C,D) immunolocalization using anti-cAPX antibodies. Courtesy of Dr. Taras Pasternak
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