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滬鼎產(chǎn)品文獻:植物MgCh,Rubisco,ELISA試劑盒引用文獻
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【文獻標題】Transcriptome profiling of genes involved in photosynthesis in Elaeagnus angustifolia L. under salt stress
【作者】J. LIN, J.P. LI, F. YUAN,et.al
【作者單位】山東師范大學(xué)（Shandong Normal University）
【文獻中引用產(chǎn)品】
植物鎂螯合酶(MgCh) ELISA試劑盒（http://www.ayijx.com/c149475/products/d4343206.html）
植物Rubisco活化酶(RCA)ELISA試劑盒（http://www.ayijx.com/c149475/products/d4343207.html）
【關(guān)鍵詞】biomass; greening; ion concentrations; photosynthetic parameters; plant height.
【DOI】https://doi.org/10.1007/s11099-018-0824-6
【影響因子(IF)】2.3
【出版期刊】《PHOTOSYNTHETICA》
【產(chǎn)品原文引用】
Protein content ａnd activity of magnesium chelatase ａnd Rubisco:
Magnesium chelatase ａnd Rubisco were prepared by first freezing a 0.2-g leaf sample in liquid nitrogen to prevent proteolytic activity, followed by grinding with 2 mL of extraction buffer (100 mM phosphate buffer, pH 7.2, containing 0.1 mM EDTA, ａnd 2 mM ascorbic acid). The homogenate was centrifuged for 15 min at 10,000 rpm, ａnd the supernatant was used to measure the protein content (ng L–1), magnesium chelatase activity [pmol(Mg-Deutero) min–1 mg–1(protein)] ａnd Rubisco activity [μmol min–1 mg–1(protein)]. Magnesium chelatase ａnd Rubisco were measured using a magnesium chelatase content kit ａnd a Rubisco content kit (double antibody sandwich method, Huding Biological Technology Co., Shanghai, China) (3 replicates per treatment).
【作者】J. LIN, J.P. LI, F. YUAN,et.al
【作者單位】山東師范大學(xué)（Shandong Normal University）
【文獻中引用產(chǎn)品】
植物鎂螯合酶(MgCh) ELISA試劑盒（http://www.ayijx.com/c149475/products/d4343206.html）
植物Rubisco活化酶(RCA)ELISA試劑盒（http://www.ayijx.com/c149475/products/d4343207.html）
【關(guān)鍵詞】biomass; greening; ion concentrations; photosynthetic parameters; plant height.
【DOI】https://doi.org/10.1007/s11099-018-0824-6
【影響因子(IF)】2.3
【出版期刊】《PHOTOSYNTHETICA》
【產(chǎn)品原文引用】
Protein content ａnd activity of magnesium chelatase ａnd Rubisco:
Magnesium chelatase ａnd Rubisco were prepared by first freezing a 0.2-g leaf sample in liquid nitrogen to prevent proteolytic activity, followed by grinding with 2 mL of extraction buffer (100 mM phosphate buffer, pH 7.2, containing 0.1 mM EDTA, ａnd 2 mM ascorbic acid). The homogenate was centrifuged for 15 min at 10,000 rpm, ａnd the supernatant was used to measure the protein content (ng L–1), magnesium chelatase activity [pmol(Mg-Deutero) min–1 mg–1(protein)] ａnd Rubisco activity [μmol min–1 mg–1(protein)]. Magnesium chelatase ａnd Rubisco were measured using a magnesium chelatase content kit ａnd a Rubisco content kit (double antibody sandwich method, Huding Biological Technology Co., Shanghai, China) (3 replicates per treatment).
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