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滬鼎產(chǎn)品文獻:鵝孕激素/孕酮(PROG)ELISA試劑盒引用文獻
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【文獻標題】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
【作者單位】四川農(nóng)業(yè)大學（Sichuan Agricultural University）
【文獻中引用產(chǎn)品】
鵝孕激素/孕酮(PROG)ELISA試劑盒（http://www.ayijx.com/c149475/products/d4342733.html）
【關(guān)鍵詞】DGAT1/2,Ovary,Progesterone secretion,Lipid metabolism,Granulosa cells
【DOI】https://doi.org/10.1016/j.jsbmb.2020.105721
【影響因子(IF)】3.8
【出版期刊】《Journal of Steroid Biochemistry ａnd Molecular Biology》
【產(chǎn)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
【作者單位】四川農(nóng)業(yè)大學（Sichuan Agricultural University）
【文獻中引用產(chǎn)品】
鵝孕激素/孕酮(PROG)ELISA試劑盒（http://www.ayijx.com/c149475/products/d4342733.html）
【關(guān)鍵詞】DGAT1/2,Ovary,Progesterone secretion,Lipid metabolism,Granulosa cells
【DOI】https://doi.org/10.1016/j.jsbmb.2020.105721
【影響因子(IF)】3.8
【出版期刊】《Journal of Steroid Biochemistry ａnd Molecular Biology》
【產(chǎn)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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