superscript ii kit (Promega)
90
Structured Review
Promega
superscript ii kit
Superscript Ii Kit, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superscript-ii+kit/superscript+ii+kit/pm29527919-78-11-14
Average 90 stars, based on 1 article reviews
Superscript Ii Kit, supplied by Promega, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/superscript-ii+kit/superscript+ii+kit/pm29527919-78-11-14
Average 90 stars, based on 1 article reviews
superscript ii kit - by Bioz Stars,
2026-11
90/100 stars
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other:Article Title: (−)-Hydroxycitric Acid Influenced Fat Metabolism via Modulating of Glucose-6-phosphate Isomerase Expression in Chicken Embryos Article Snippet: The current research aimed to explore the impact of (-)-hydroxycitric acid (HCA) 12 on fat metabolism and investigate whether this action of (-)-HCA associated with modulation 13 of glucose-6-phosphote isomerase (GPI) expression in chicken embryos.. We constructed 14 recombinant plasmid (sh2-GPI) to inhibit GPI expression, and then embryos were treated with 15 (-)-HCA.. Results showed that (-)-HCA reduced lipid droplets accumulation, triglyceride 16 content, lipogenesis factors mRNA level and increased lipolysis factors mRNA expression, 17 while this effect caused by (-)-HCA was markedly reversed when the chicken embryos were 18 pretreated with sh2-GPI. (-)-HCA increased phospho (p)-acetyl-CoA carboxylase, enoyl-CoA 19 hydratase short chain-1, carnitine palmitoyl transferase 1A, p-AMP-activated protein kinase, 20 and peroxisome proliferators-activated receptor α protein expression, and this action of 21 (-)-HCA also dispelled when the chicken embryos were pretreated with sh2-GPI. Article Title: Potential role of ALDH3A2 on the lipid and glucose metabolism regulated by (-)-hydroxycitric acid in chicken embryos. Article Snippet: As one of the main sources of animal protein for humans (Malley, Butts, & Wiedmann, 2015), the increasing demand for chicken prod‐ ucts resulted in pursuit of growth rate and often ignores fat deposition in poultry production.. Excessive fat deposition needs to be controlled, since it reduces meat quality as well as the negative effect on con‐ sumers who have increased risk of diabetes, cardiovascular disease, hypertension, and fatty liver disease from dietary fat intake (Ji et al., 2012).. Due to the economic concerns and consumer aversion to ex‐ cess fat deposition, many studies had focused on various approaches to control fat deposition and improve meat quality via supplemental with bioactive compounds in poultry production. (‐)‐Hydroxycitric acid ((‐)‐HCA), extracted from the dried fruit rind of Garcinia cambogia, has demonstrated to reduce body weight gain (Fassina et al., 2015), inhibit de novo fatty acid synthesis (Chuah, Received: 2 March 2019 | Revised: 10 April 2019 | Accepted: 18 April 2019 DOI: 10.1111/asj.13225 Article Title: (-)-Hydroxycitric acid regulates energy metabolism by activation of AMPK - PGC1α - NRF1 signal pathway in primary chicken hepatocytes. Article Snippet: As the most important bioactive substance in Garcinia cambogia, (−)-hydroxycitric acid (HCA) is widely used in food additives to regulate obesity and diabetes in animals or humans, while the mechanism is poorly understood.. The purpose of this study was to elucidate the regulatory effect and mechanism of (−)-HCA in regulating glucose and lipid metabolism in chicken primary hepatocytes.. The results showed that (−)-HCA obviously decreased triglyceride content through inhibiting the fatty acid synthase protein level, and enhancing the protein level of phosphorylated acetyl CoA carboxylase, enoyl coenzyme A hydratase short chain 1 and carnitine palmitoyltransferase 1A in hepatocytes. Reverse Transcription:Article Title: Dehydroepiandrosterone Prevents H 2 O 2 -Induced BRL-3A Cell Oxidative Damage through Activation of PI3K/Akt Pathways rather than MAPK Pathways Article Snippet: BRL-3A cells were grown in 6-well plates (1 × 10 6 cells per well) and treated with 0, 1, 10, or 100 μ M DHEA for 24 h, then they were exposed to 150 μ M H 2 O 2 for another 2 h. After incubation, the cells were harvested and total RNA was extracted using the TRIZOL reagent kit (Invitrogen, USA) according to the manufacturer's protocols. .. Article Title: 4-Octyl Itaconate Prevents Free Fatty Acid-Induced Lipid Metabolism Disorder through Activating Nrf2-AMPK Signaling Pathway in Hepatocytes. Article Snippet: .. Briefly, total RNA was reverse transcribed into cDNA using the Article Title: Effect of dehydroepiandrosterone on the immune function of mice in vivo and in vitro. Article Snippet: Dehydroepiandrosterone (DHEA) has anti-inflammatory, anti-oxidant and immune-regulating properties, while the mechanism of DHEA actions remains unclear.. The present study aims to investigate the effect and possible mechanism of DHEA on immune function of mice in vivo and in vitro.. In vivo, a lipopolysaccharide (LPS)-induced experimental inflammation model was constructed to analyze the regulation of DHEA on anti-oxidative and immune function in ICR mice; In vitro, the effects of DHEA on the biological functions of lymphocytes and macrophages were studied. Article Title: Dehydroepiandrosterone rehabilitate BRL-3A cells oxidative stress damage induced by hydrogen peroxide. Article Snippet: Funding information Priority Academic Program Development of Jiangsu Higher Education Institutions; National Natural Science Foundation of Jiangsu, Grant number: NO. BK20151434 This study aimed to investigate the molecular mechanism of dehydroepiandrosterone (DHEA) rehabilitated BRL-3A cells oxidative stress damage induced by hydrogen peroxide (H2O2).. Results showed that DHEA reversed the decrease of cell viability and ameliorated nuclear chromatin damage in H2O2-induced BRL-3A cells.. DHEA increased the activities of superoxide dismutase, catalase, peroxidase, and glutathione peroxidase, and decreased the reactive oxygen species (ROS) production in H2O2induced BRL-3A cells. |