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沪鼎产品文献:鹅孕激素/孕酮(PROG)ELISA试剂盒引用文献
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【文献标题】Differential actions of diacylglycerol acyltransferase (DGAT) 1 ａnd 2 in
regulating lipid metabolism ａnd progesterone secretion of goose granulosa cells
【作者】Shenqiang Hu, Shanyan Gao, Jiaran Zhu,et.al
【作者单位】四川农业大学（Sichuan Agricultural University）
【文献中引用产品】
鹅孕激素/孕酮(PROG)ELISA试剂盒（http://www.ayijx.com/c149475/products/d4342733.html）
【关键词】DGAT1/2,Ovary,Progesterone secretion,Lipid metabolism,Granulosa cells
【DOI】https://doi.org/10.1016/j.jsbmb.2020.105721
【影响因子(IF)】3.8
【出版期刊】《Journal of Steroid Biochemistry ａnd Molecular Biology》
【产品原文引用】
Progesterone measurement
The steroids from 0.05?0.1 g of each thoroughly mixed yolk sample were extracted with 1 mL diethyl ether ａnd purified by a precipitation with 1 mL 95 % ethanol to remove excess lipids. Progesterone levels in the extracts were then measured using goose progesterone ELISA kit (Shanghai Huding Biotechnology Co., Ltd., Shanghai, China) according to the manufacturer’s instruction, ａnd total progesterone levels in each follicle were calculated as [(the total levels of progesterone in the extract ÷ the weight of yolk subjected to extraction) × the total weight of yolk isolated from this follicle] ａnd were expressed as pmol/follicle. Levels of progesterone in culture media were also measured using goose progesterone ELISA kit (Shanghai Huding Biotechnology Co., Ltd., Shanghai, China). Serial dilutions of media samples showed good linearity (differed by 15 % or less) in the calculated concentrations of progesterone, ａnd the detection limit of progesterone is 7 pmol/L. Relative progesterone level was expressed as the fold difference vs. cells treated with the siRNA-NC or the pEGFP-N1 empty plasmid
regulating lipid metabolism ａnd progesterone secretion of goose granulosa cells
【作者】Shenqiang Hu, Shanyan Gao, Jiaran Zhu,et.al
【作者单位】四川农业大学（Sichuan Agricultural University）
【文献中引用产品】
鹅孕激素/孕酮(PROG)ELISA试剂盒（http://www.ayijx.com/c149475/products/d4342733.html）
【关键词】DGAT1/2,Ovary,Progesterone secretion,Lipid metabolism,Granulosa cells
【DOI】https://doi.org/10.1016/j.jsbmb.2020.105721
【影响因子(IF)】3.8
【出版期刊】《Journal of Steroid Biochemistry ａnd Molecular Biology》
【产品原文引用】
Progesterone measurement
The steroids from 0.05?0.1 g of each thoroughly mixed yolk sample were extracted with 1 mL diethyl ether ａnd purified by a precipitation with 1 mL 95 % ethanol to remove excess lipids. Progesterone levels in the extracts were then measured using goose progesterone ELISA kit (Shanghai Huding Biotechnology Co., Ltd., Shanghai, China) according to the manufacturer’s instruction, ａnd total progesterone levels in each follicle were calculated as [(the total levels of progesterone in the extract ÷ the weight of yolk subjected to extraction) × the total weight of yolk isolated from this follicle] ａnd were expressed as pmol/follicle. Levels of progesterone in culture media were also measured using goose progesterone ELISA kit (Shanghai Huding Biotechnology Co., Ltd., Shanghai, China). Serial dilutions of media samples showed good linearity (differed by 15 % or less) in the calculated concentrations of progesterone, ａnd the detection limit of progesterone is 7 pmol/L. Relative progesterone level was expressed as the fold difference vs. cells treated with the siRNA-NC or the pEGFP-N1 empty plasmid
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