Titlebook: ROS Signaling in Plants ; Methods and Protocol Francisco J. Corpas,José M. Palma Book 2024 The Editor(s) (if applicable) and The Author(s),

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書目名稱ROS Signaling in Plants 影響因子(影響力)




書目名稱ROS Signaling in Plants 影響因子(影響力)學(xué)科排名




書目名稱ROS Signaling in Plants 網(wǎng)絡(luò)公開度




書目名稱ROS Signaling in Plants 網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱ROS Signaling in Plants 被引頻次




書目名稱ROS Signaling in Plants 被引頻次學(xué)科排名




書目名稱ROS Signaling in Plants 年度引用




書目名稱ROS Signaling in Plants 年度引用學(xué)科排名




書目名稱ROS Signaling in Plants 讀者反饋




書目名稱ROS Signaling in Plants 讀者反饋學(xué)科排名

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Francisco J. Corpas,José M. PalmaIncludes cutting-edge techniques.Provides step-by-step detail essential for reproducible results.Contains key implementation advice from the experts

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Common Methods of Extraction and Determination of Phytomelatonin in Plants,is on the techniques of extraction, cleaning, separation, detection, identification, and quantification. Multiple examples and recommendations are presented for a clear overview of the pros and cons of phytomelatonin determinations in plant tissues, seeds, and fruits, mainly.

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Detection of Ascorbate Peroxidase (APX) Activity in Plant Tissues: Using Non-denaturing PAGE and Sping polyacrylamide gel electrophoresis (PAGE) in combination with a spectrophotometric assay for APX activity, the protocol allows identifying diverse APX isozymes present in different organs and plant species.

炸壞

Determination of ROS Generated by , Xanthine Dehydrogenase1 (AtXDH1) Using Nitroblue Tetrazolium (Nch as nitrogen starvation, wounding, or UV-C. Additionally, we describe the use of NBT staining for detecting enzymatic generation of ROS in native and native SDS PAGE gels. Our protocol also outlines the separation and comparison of the origin of ROS generated by xanthine dehydrogenase1 (XDH1) using different substrates.

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Inactivation of Three Stacked Genes of Cytosolic Peroxiredoxins by Genome Editing, in close vicinity on chromosome 1 so that crossing over between the genes most rarely occurs and successful crossing of the plants appears impossible. Genome editing instead allows targeting of multiple isoforms and knocks out several genes at once. This chapter describes how to inactivate the three cytosolic peroxiredoxins by CRISPR/Cas9 in ..