cell confluence (Sartorius AG)
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Sartorius AG
cell confluence
Cell Confluence, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 15815 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cell+confluence/Live+Cell+Analysis+Instruments/pm42055283-96-11-20
Average 99 stars, based on 15815 article reviews
Cell Confluence, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 15815 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cell+confluence/Live+Cell+Analysis+Instruments/pm42055283-96-11-20
Average 99 stars, based on 15815 article reviews
cell confluence - by Bioz Stars,
2026-09
99/100 stars
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Fluorescence:Article Title: SLX1 Inhibition Enhances Olaparib Sensitivity by Impairing Homologous Recombination Repair in Breast Cancer. Article Snippet: After 24 h, cells were treated with the indicated compounds, and Incucyte® Annexin V Green Reagent (4642, Sartorius, Göttingen, Germany) was added according to the manufacturer’s instructions. .. Plates were placed in the Incucyte® SX5 Live-Cell Analysis System (Sartorius), and phase-contrast and fluorescence images were automatically acquired every 6 h for up to 72 h. Green fluorescent object area (Annexin V-positive cells) was quantified and normalized to Software:Article Title: SLX1 Inhibition Enhances Olaparib Sensitivity by Impairing Homologous Recombination Repair in Breast Cancer. Article Snippet: After 24 h, cells were treated with the indicated compounds, and Incucyte® Annexin V Green Reagent (4642, Sartorius, Göttingen, Germany) was added according to the manufacturer’s instructions. .. Plates were placed in the Incucyte® SX5 Live-Cell Analysis System (Sartorius), and phase-contrast and fluorescence images were automatically acquired every 6 h for up to 72 h. Green fluorescent object area (Annexin V-positive cells) was quantified and normalized to Article Title: The genetic and biochemical basis of human leading strand synthesis. Article Snippet: .. Medium was then replaced with fresh one and plates 620 were incubated in an IncuCyte® S3 Live-Cell Analysis System (Sartorius) at 37 °C for 621 120 h. The first image was captured 3 h after inserting plate into the equipment and 622 the 10 X objective captured 4 fields of view every 3 h. Cell Analysis:Article Title: Targeting multiple genetic defects of mitochondrial diseases with a single bacterial lipoate protein ligase Article Snippet: .. Article Title: Targeting multiple genetic defects of mitochondrial diseases with a single bacterial lipoate protein ligase. Article Snippet: .. other:Article Title: Personalized chronotherapy in glioblastoma: integrating circadian profiling and PK–PD modelling to optimize temozolomide timing Article Snippet: Cell confluence was measured every 2 h using the Live Cell Imaging:Article Title: A novel bispecific siRNA concept: Efficient dual knockdown of YAP1 and WWTR1 with a single guide strand Article Snippet: At 5 or 7 days post transfection, cell viability was assessed using the CellTiter-Glo 2.0 Assay (Promega, Madison, WI, USA, G9241), with luminescence measured on an EnSight plate reader (PerkinElmer, Waltham, MA, USA). .. Incubation:Article Title: The genetic and biochemical basis of human leading strand synthesis. Article Snippet: .. Medium was then replaced with fresh one and plates 620 were incubated in an IncuCyte® S3 Live-Cell Analysis System (Sartorius) at 37 °C for 621 120 h. The first image was captured 3 h after inserting plate into the equipment and 622 the 10 X objective captured 4 fields of view every 3 h. |
![( a) LC-MS of His levels in NMG (n = 7) and MMTV-c- Myc (n = 10) tumours after a 5 min [U 13 C]His bolus. Total abundance (left) and isotopologue distribution (right). Mean ± s.d.; p -values from two-way ANOVA (Šídák’s correction). ( b) Timeline: cells cultured in 2.0 or 0.1 mM Gln (24 h) before 20-min [U 13 C]His administration. ( c) Total relative His abundance (n = 3). Data are mean ± s.d.; p -values from two-way ANOVA (Šídák’s correction). ( d ) RT-qPCR of indicated genes expression in cells cultures in 2.0 mM or 0.1 mM Gln (n = 3), normalized to β-actin and expressed relative to 2.0 mM Gln. Mean ± s.d.; p -values from one-way ANOVA (Šídák’s correction). ( e,f ) WB of cells in 2.0 mM or 0.1 mM Gln (24 h), n = 3; in ( f ) MMTV-c- Myc tumour and liver tissue are used as controls. ( g ) Relative <t>confluency</t> of cells in 0-2.0 mM Gln (96 h), normalized to 2.0 mM Gln; IC50 values from non-linear fit of log[Gln] vs. normalized response (n = 2). ( h ) LC-MS of cells in 2.0 mM or 0.1 mM Gln (24 h), followed by a 10 min [U 13 C]His pulse (n = 3). Labelled His abundance is relative to 2.0 mM Gln. Mean ± s.d.; p -values from one-way ANOVA (Šídák’s correction). See also Figure S2.](https://bio-rxiv-images-cdn.bioz.com/dois_ending_with_93/10__64898_slash_2026__04__15__716193/10__64898_slash_2026__04__15__716193___F2.large.jpg)
