Chub-s7
WebNov 19, 2024 · Human pre-adipocytes cell line (Chub-S7) and primary adipocytes were obtained from lean, obese and morbid obese patients, grown to confluence, differentiated for one week, maintained in nutrition media for next 7 days (day 14) and then used for further experimental analysis. In order to analyse B12 deficiency effects, customized media with ... WebApr 4, 2024 · Our results are in line with those by Gathercole et al. , who reported increased insulin-stimulated glucose uptake in a human immortalized subcutaneous adipocyte line (Chub-S7) after acute exposure to dexamethasone, as well as to hydrocortisone (up to 48 hours, in a dose- and time-dependent manner for the latter), thus proposing that the ...
Chub-s7
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WebJan 31, 2011 · Chub-s7 cell line. Proliferating chub-s7 cells were cultured in Dulbecco's MEM/Nutrient Mixture F-, DMEM-F12 (Sigma, Poole, UK) … WebNov 25, 2024 · The aim of our study was to use a combined epigenomic and transcriptomic approach to identify novel genes mediating the effect of B12 on adipogenesis.Human pre …
WebMar 1, 2006 · Chub-S7 cells were growing as previously described [11]. SVF cells enriched in primary preadipocytes were prepared according to the method described by Rodbell [13]. Briefly, subcutaneous adipose tissues derived from obese subjects were digested for 15–20 min at 37 °C in DMEM medium containing 2 mg/ml collagenase WebNov 1, 2013 · The Chub-S7 cell line (Nestlé Research Centre, Lausanne, Switzerland) was derived from human subcutaneous adipose tissue by coexpression of human telomerase reverse transcriptase and papillomavirus E7 oncoprotein (HPV-E7) genes ( 14) and has previously been characterized in detail showing expression of typical white adipose …
Web> chub s7 cells. micrococcal nuclease mnase About; News; Press Release; Team; Advisors; Partners; Contact; Bioz Stars; Bioz vStars; 86 : Buy from Supplier : Structured … WebMay 7, 2024 · In order to validate the findings from human adipocyte cell line ChubS-7, the key experiments were also performed in cultured primary human adipocytes under the same conditions. The total cholesterol as well as homocysteine was significantly increased in primary adipocytes in the LB and NoB conditions compared with control .
WebChub-S7 cells and primary cultures of human sc preadipocytes differentiate in chemical defined media (14 d) and acquire a mature adipocyte phenotype with clearly visible lipid droplets.
WebFeb 9, 2024 · A human adipocyte cell model, Chub-S7, was used to address the intracellular change in Lp-PLA2 in adipocytes. Results Lp-PLA2 and calcium-independent PLA2 (iPLA2) isoforms were altered by adiposity, … oops tablewareWebNov 25, 2024 · Culture and differentiation of human pre-adipocytes in CHUB-S7 for discovery and validation experiments. Human preadipocyte cell line Chub-S7 were cultured and differentiated as previously described [6, 11)). The respective DMEM/F12 growth media for each condition was changed every 48 hours until 100% confluence was achieved. oops technologies incWebTo determine whether Chub-S7 cells were able to differenti-ate, the expression of adipocyte markers was assessed, by real-time RT-PCR, at different time points during cellular iowa code chapter 81WebApr 14, 2014 · After 17 days of differentiation, fully differentiated Chub-S7 cells were treated with the estrogen receptor alpha agonist 4,4′,4″- (4-Propyl- [1H]-pyrazole-1,3,5-triyl) trisphenol (PPT) (1426-Tocris, Bristol, U.K.) in DMEM media (D6046-Sigma-Aldrich). A vehicle DMSO control was included. iowa code crossing center lineWebAug 22, 2003 · The immortalized Chub-S7 cells displayed a comparable proliferation rate and a similar doubling time to human primary stromal cells, 13 suggesting a limited deregulation of cell cycle checkpoints ... iowa code chapter 71WebMillipore 7 15 d s7 nkx6 1 insulin mafa cells. 7 15 D S7 Nkx6 1 Insulin Mafa Cells, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed … oop static methodWebMethods: ER stress was induced in post-differentiated Chub-S7 (AbdSc Ad) using tunicamycin (Tn) (0.25 μg/ml, 0.75 μg/ml) for 24 hrs, 48 hrs and 72 hrs. Assessment of mitochondrial function post Tn treatment was undertaken using the Extracellular Flux Analyser – evaluating oxygen consumption rate (OCR) and proton excretion (glycolysis ... iowa code chapter 679a