山東師范大學使用我司試劑盒發表文獻合集
日期:2025-08-19瀏覽:195次
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【文獻標題】Regulatory network of lncRNAs and mRNAs explains why salinity promotes photosynthesis and plant growth in the halophyte Suaeda salsa
【作者】Chenyang Li a, Runtai Zhao a, Bing Cuiet.al
【作者單位】Shandong Normal University 山東師范大學
【文獻中引用產品】
植物甘油醛-3-磷酸脫氫酶(GAPDH)ELISA試劑盒 活性
植物二磷酸核酮糖羧化酶(RuBPCase)ELISA試劑盒 活性
【關鍵詞】Carbon metabolism、Halophyte、lncRNA、Photosynthesis、Salinity、Suaeda salsa
【DOI】doi.org/10.1016/j.jplph.2025.154493
【出版期刊】《Journal of Plant Physiology》
【產品原文引用】
Take the leaves of S. salsa treated with 0 mM as control and 200 mM NaCl for 24 h, and configure the GAPDH and Rubisco enzyme activity detection systems according to the instructions of the plant glyceraldehyde-3-phosphate dehydrogenase (GAPDH) enzyme-linked immunosorbent assay (ELISA) kit and RuBPCase ELISA kit (Shanghai Huding Biotechnology Co., Ltd., Shanghai, China).
【文獻標題】Photosynthetic evidence from Suaeda glauca explains why seedlings of this species from saline soils has higher biomass than that from non-saline soils
【作者】Chenyang Li , Menghan Wu, Bing Cui et.al
【作者單位】Shandong Normal University(山東師范大學)
【文獻中引用產品】
植物3-磷酸甘油醛脫氫酶(GAPDH)ELISA試劑盒
【關鍵詞】Carbon assimilation ,Halophyte ,Photoreaction ,RNA-seq ,Suaeda glauca
【DOI】doi.org/10.1016/j.indcrop.2024.118119
【出版期刊】《Industrial Crops and Products》
【產品原文引用】
A total of 0.3 g of mature leaves was crushed in a pre-cooled mortar and ground on ice with 2.7 ml of 10 mM chilled PBS buffer, pH 7.3. The supernatant was removed by centrifugation and stored at ? 20 ?C for later use. The activity of GAPDH was assayed using a plant glyceraldehyde 3-phosphate dehydrogenase (GAPDH) enzyme-linked immunosorbent assay (ELISA) kit (Shanghai Huding Biotechnology Co., Ltd., Shanghai, China).
【文獻標題】Effect of non-uniform root salt distribution on the ion distribution and growth of the halophyte Suaeda salsa
【作者】Chenyang Li , Xinxin Zhang , Xiaolei Yang et.al
【作者單位】Shandong Normal University(山東師范大學)
【文獻中引用產品】
植物激素脫落酸(ABA)ELISA試劑盒
【關鍵詞】Halophyte,Non-uniform salt,Nitrate,Split-root system,Suaeda salsa
【DOI】doi.org/10.1016/j.marpolbul.2024.116754
【出版期刊】《Marine Pollution Bulletin》
【產品原文引用】
Lateral roots (0.3 g in each replicate) were used to measure ABA concentration according to the steps of the phytohormone abscisic acid (ABA) ELISA kit (Cat. No.: D-60004, Shanghai Huding Biotechnology Co., Ltd., Shanghai), and the absorbance was measured at 450 nm using a Spectra Max M5 microplate reader (Molecular Devices, USA)
【文獻標題】Positive effects of NaCl on the photoreaction and carbon assimilation efficiency in uaeda salsa
【作者】Qiang Li, Ru Liu, Zihan Li, Hai Fanet.al
【作者單位】山東師范大學 Sangdong Normal University
【文獻中引用產品】
植物鐵氧還蛋白-NADP氧化還原酶(FNR)活性
【關鍵詞】Abbreviations: Electron transport rate, ETR; Ferredoxin-NADP oxidoreductase, FNR; Ribulose-1 5-bisphosphate carboxylase, Rubisco; Rubisco activase, RCA.
【DOI】doi.org/10.1016/j.plaphy.2022.02.019
【出版期刊】《Positive effects of NaCl on the photoreaction and carbon assimilation efficiency in uaeda salsa》
【產品原文引用】Determination of the activities of ferredoxin-NADP oxidoreductase, ribulose-1,5-bisphosphate arboxylase and Rubisco activase A total of 0.3 g of mature leaves were placed in a pre-cooled mortar, and the leaves were ground on ice with chilled 50 mM Tris buffer at pH 7.4. The supernatant was extracted by centrifugation and stored at -20 °C. The activity of FNR was assayed using a plant ELISA kit (Shanghai Huding Biotechnology Co., Ltd., Shanghai, China). A microplate reader (Spectra Max M5; Molecular Devices, San Jose, CA, USA) was used to assay the activity of the enzyme according to the manufacturer’s instructions (Zhao et al., 2018). Three replicates were established for each concentration of NaCl.The activities of Rubisco and RCA were assayed as described for FNR.
【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(Shandong Normal University)
【文獻中引用產品】
植物鎂螯合酶(MgCh) ELISA試劑盒
植物Rubisco活化酶(RCA)ELISA試劑盒
【關鍵詞】biomass; greening; ion concentrations; photosynthetic parameters; plant height.
【DOI】doi.org/10.1007/s11099-018-0824-6
【出版期刊】《PHOTOSYNTHETICA》
【產品原文引用】
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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