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cytation 5 cell imaging multimode reader biotek  (R&D Systems)


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    R&D Systems cytation 5 cell imaging multimode reader biotek
    Cytation 5 Cell Imaging Multimode Reader Biotek, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cell+lysis+buffer+5/Cell+Lysis+Buffer+5+(1+x+15+mL)/pm40639678-92-23-36
    Average 93 stars, based on 12 article reviews
    cytation 5 cell imaging multimode reader biotek - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Lysis:

    Article Title: N-acyl glycines produced by commensal bacteria potentiate GLP-1 secretion as GPCR ligands.
    Article Snippet: Commensal microbiota is crucial for nutrient digestion and production of biologically active molecules, many of which mimic endogenous ligands of human GPCRs.. Bacteroides spp. are among the most abundant bacteria residing in the human gut and their absence has been positively correlated with metabolic disorders.. In the present study, we focused on N-acylated glycines (NAGlys) as products of Bacteroides spp. and potential GPCR ligands modulating GLP-1 secretion.

    Article Title: Effects of asprosin on estradiol and progesterone secretion and proliferation of bovine granulosa cells.
    Article Snippet: Asprosin is an adipokine synthesized by the white adipose tissue that regulates glucose homeostasis and that has been reported to affect bovine theca cell function and follicular growth, but its role on granulosa cell functions remains to be unveiled.. Hence, the objective of this study was to investigate asprosin impacts on granulosa cell steroidogenesis.. Bovine granulosa cells from small ovarian follicles were cultured in vitro to investigate the effects of asprosin on cell proliferation, production of steroids, mRNA abundance of genes that encode steroidogenic enzymes and cell cycle regulators, and protein relative abundance of steroidogenic signaling pathways.



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