Cell / Nature正刊引用鑒賞,厲害了小鼠胰島素ELISA試劑盒
胰島素在細(xì)胞水平的生物作用是通過(guò)與靶細(xì)胞膜上的特異受體結(jié)合而啟動(dòng)的。胰島素受體為胰島素起作用的靶細(xì)胞膜上特定部位,僅可與胰島素或含有胰島素分子的胰島素原結(jié)合,具有高度的特異性,且分布非常廣泛。
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胰島素幾乎直接或間接地影響著機(jī)體每個(gè)組織的功能,其中胰島素三大主要能量?jī)?chǔ)存組織的代謝效應(yīng),即肝臟、肌肉和脂肪組織。
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(1)胰島素與葡萄糖代謝 — 葡萄糖的三大來(lái)源是:食物的腸道吸收,糖原分解(糖原是葡萄糖的儲(chǔ)存形式),以及糖異生(碳水化合物、蛋白質(zhì)和脂肪代謝過(guò)程中生成的非糖前體成分可經(jīng)糖異生作用合成葡萄糖)。
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(2)胰島素與脂代謝 — 胰島素能夠協(xié)調(diào)體內(nèi)不同能源物質(zhì)(葡萄糖和游離脂肪酸)的利用,來(lái)滿足機(jī)體在進(jìn)食與空腹的循環(huán)中以及運(yùn)動(dòng)時(shí)的能量需求。進(jìn)餐后有大量葡萄糖可用,此時(shí)胰島素分泌增加,這可促進(jìn)甘油三酯儲(chǔ)存至脂肪細(xì)胞。
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(3)胰島素與蛋白質(zhì)代謝 — 胰島素增加氮貯留和蛋白質(zhì)生成。
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如何尋找一款小鼠胰島素ELISA試劑盒呢?由眾多Cell,Nature文章引用的艾美捷?Crystal Chem小鼠胰島素ELISA試劑盒給你答案~
Crystal Chem小鼠胰島素ELISA試劑盒:超靈敏,一個(gè)kit,3種標(biāo)曲范圍自由組合、適用樣本類型齊全、簡(jiǎn)單省時(shí),肉眼可見(jiàn)的性價(jià)比(哈哈哈~)
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Cell / Nature正刊引用鑒賞:
1、Cell [ IF=41.58 ],CerS6-Derived Sphingolipids Interact with Mff and Promote Mitochondrial Fragmentation in Obesity. 2019 May 30;177(6):1536-1552.e23. doi: 10.1016/j.cell.2019.05.008.
2、Nature [IF=49.96],Inceptor counteracts insulin signalling in?β-cells to control glycaemia, 2021 Feb;590(7845):326-331. doi: 10.1038/s41586-021-03225-8.
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其它發(fā)表文章(僅摘取部分展示):
Mani, Bharath K., et al. "Hypoglycemic effect of combined ghrelin and glucagon receptor blockade." Diabetes 2017; 66: 1847-1857.
Marcondes, Rodrigo R., et al. "Exercise differentially affects metabolic functions and white adipose tissue in female letrozole- and dihydrotestosterone-induced mouse models of polycystic ovary syndrome." Molecular and Cellular Endocrinology 2017; 448: 66-76.
McPherson, Nicole O., et al. "An exercise-only intervention in obese fathers restores glucose and insulin regulation in conjunction with the rescue of pancreatic islet cell morphology and microRNA expression in male offspring." Nutrients 2017; 9: 122. ?Thrailkill, Kathryn M., et al. "The impact of SGLT2 inhibitors, compared with insulin, on diabetic bone disease in a mouse model of type 1 diabetes." Bone 2017; 94: 141-151.
Tanigaki, Keiji, et al. "Endothelial Fcγ?receptor IIB activation blunts insulin delivery to skeletal muscle to cause insulin resistance in mice." Diabetes 2016; 65: 1996-2005.