CellTiter-Glo 2.0 Assay G9243 from Promega

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ItemCellTiter-Glo 2.0 Assay
CompanyPromega
Price Supplier Page View Company Product Page
Catalog NumberG9243
Quantity500ml

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Promega

2800 Woods Hollow Rd

Madison, WI 53711

United States

Phone: Tel: +1 (608) 274-4330
Fax: +1 (608) 277-2516

Email: custserv@promega.com
techserv@promega.com

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Website: http://www.promega.com

(1) Tramadol induced hypoxia signaling and paraptosis-like cell death in breast cancer cells via HIF-1α and ATF4 dependent pathwaysRedox ReportDecember 31, 2026Zih-Syuan Wu, Shih-Ming Huang, Yi-Hsuan HuangMadison, WI, USA), whereas cell viability was measured using the CellTiter-Glo® 2.0 Assay (catalog no.: G9241; Promega). Fluorescence or luminescence signals were detected using a Varioskan LUX plate reader (Thermo Fisher Scientific

(2) 3D matrix stiffness drives energy metabolism to orchestrate stem cell osteogenesis via microtubule acetylation and mitochondrial dynamicsBioactive MaterialsNovember 1, 2026Zhijie Yang, Jing Na, Yu Liu, Gan Yue, Fei Song, Chiyu Li, Qiusheng Shi, Yubo Fan, Lisha Zhengcells per 100 μl. 100 μl cell suspension and 100 μl CellTiter-Glo® 2.0 Cell Viability Assay reagent (G9241, Promega, WI, USA) were mixed rapidly in opaque 96-plates and the luminescent output was detected by

(3) A critical role for mitochondrial dynamics in cigarette smoke condensate-induced RPE senescenceFree Radical Biology and MedicineOctober 1, 2026Qi Zhou, Zunyi Zhang, Yinga Wu, Chunmin Dong, Chen-Chuan Wu, James T. Handa, Jing Ma, Shusheng WangMitoSOX loading. Cellular ATP level was measured as described in the CellTiter-Glo 2.0 Assay kit (Promega G9242). Briefly, ARPE-19 cells were seeded using opaque-walled 96-well plates with 100 μl of culture medium,

(4) An Injectable, Self-Expanding Hemostatic Foam for Field-Compatible Postpartum Hemorrhage ManagementAdv Sci (Weinh)September 27, 2026Charlotte Meyer, Noël Strasser, Ilakkiya Ravindrarajah, Elsa Wrenger, Kristian Ivkovic, Jan Ševčík, Sima Šarčević, Lenka Červenková, Jáchym Rosendorf, Václav Liška, et al.24 h. Cell viability was assessed through the ATP dependent CellTiter‐Glo 2.0 Cell Viability Assay (#G9241, Promega, Dübendorf, Switzerland) and cytotoxicity was measured using the LDH dependent CytoTox 96 Cytotoxicity

(5) RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulationSci AdvSeptember 25, 2026Pushpamali De Silva, Samantha Fitzgerald, Jules Cazaubiel, Kristin Qian, Matan Hofree, Jia-Ren Lin, Roxanne Pelletier, Mariana Lopez Leon, Phuong Vu Mai Ho, Yasutoshi Takashima, et al.Cell viability was determined using the CellTiter-Glo 2.0 Cell Viability Assay (Promega, catalog no. G9242) for 2D cultures and the CellTiter-Glo 3D Cell Viability Assay (Promega, catalog no. G9681) for 3D cultures,

(6) Autophagy inhibition sensitizes radiotherapy responses in high-grade mutant IDH1 gliomaNat CommunSeptember 18, 2026Felipe J. Núñez, Kaushik Banerjee, Anzar A. Mujeeb, Ava Mauser, Claire E. Tronrud, Ziwen Zhu, Sadhakshi Raghuram, Maya R. Sheth, Jorge Armando Pena Agudelo, Julio Zelaya, et al.post-inhibitor treatment. Cell viability was evaluated 72 h post-IR treatment using CellTiter-Glo 2.0 (Promega, G9242) luminescence cell viability assay, following the manufacturer’s protocol. The resulting luminescence

(7) A novel p53R273H-Selective Bispecific T-Cell Engager: from Clinical TCR clone to Computational Optimization and Functional ValidationMolecular Therapy OncologySeptember 17, 2026Nhan Huynh, Thu-My Thi Nguyen, Ngoc Thi Bui, Thao-Nguyen Ho Nguyen, Diem T.P. Tran, Hoai-Nghia Nguyen, Cuong Thach Nguyenand target cells were subjected to luminescence-based cytotoxicity assay using Celltiter-Glo (Promega G9242). Both functional assays were done following the manufacturer’s instructions. In silico peptide evaluation

(8) KDM4B Maintains Pyruvate Dehydrogenase Complex Expression to Support Mitochondrial Metabolism and Survival in Cancer CellsEpigenomesSeptember 16, 2026Sachiko Sato, Arif Ul Hasan, Mami Obara, Eiichi TairaCellTiter-Glo Luminescent Cell Viability Assay Cell viability was independently evaluated using the CellTiter-Glo Luminescent Cell Viability Assay (G9242, Promega, Madison, WI, USA) according to the manufacturer’s instructions. The reagent was added directly

(9) Functional impact of Nth like DNA glycosylase 1 on mitochondrial dynamicsNucleic Acids ResSeptember 15, 2026Lisa Hubers, Alexander Myhr Skjetne, Luisa Luna, Yohan Lefol, Solveig Osnes Lund, Ane Marit Wågbø, Xavier Renaudin, Annikka Polster, Zoe J da Silva, Anders Knoph Berg-Eriksen, et al.iodide positive. Cell viability was measured with the CellTiter-Glo® 2.0 Cell Viability Assay (Promega, G9243) at 25% final concentration using SPARK® Multimode Microplate Reader (Tecan) to measure luminescence.

(10) The long non-coding RNA, CyKILRb, acts as a competing endogenous RNA for tumor suppressive microRNAs to augment oncogenic phenotypes via induction of the PIK3R2/PI3K/AKT axisMolecular Therapy Nucleic AcidsSeptember 8, 2026Xiujie Xie, H. Patrick Macknight, Barbara Dziegielewska, Amy L. Lu, Ngoc Thanh Vu, Charles E. ChalfantCell Titer-Glo 2.0 Assay Kit and Dual-Luciferase Reporter Assay System were purchased from Promega (G9242 and E1910). Biotin labled miR-control and miR-3151-5p were synthesized from Horizon. The mycoplasma

(11) Estrogen promotes tumor phenotypes in ER+ and ER- breast cancer through UGDH-GPR30JCI InsightSeptember 8, 2026Meghan J. Price, Annee D. Nguyen, Corinne H. Strawser, Trupti Trivedi, Cesar C.D. Baeta, Catherine Lavau, Jovita K. Byemerwa, Debarati Mukherjee, Suzanne E. Wardell, Sandeep Artham, et al.either 1 nM E2 or continued 10% CS media. Cell viability assays were performed using CellTiter-Glo (G9241, Promega); reading was taken at baseline (pretreatment) and daily until day 6. Wound healing assay Cells

(12) Comparative in vitro safety assessments of synthetized and plant-derived cannabidiol (CBD), and pharmacokinetics of synthetized CBD: evidence of similar toxicological profiles and accumulation upon repeated oral administrationFront ToxicolSeptember 4, 2026E. T. Wong, D. Bovard, W. K. Schlage, W. Xia, H. Isa, O. Sirbu, A. R. Kolli, G. N. Nikolajsen, S. S. Jensen, J. Ho, et al.condition. Cell viability, and the EC50, was measured using the CellTiter-Glo® 2.0 ATP assay (Ref. G9241, Promega, Madison, WI, USA) on Day 14 of treatment. After removing the medium, 50 µL of serum-free medium

(13) Antibacterial and Anticancer Evaluation of Copper-Aluminum (CuAl) Layered Double Hydroxides (LDH) Synthesized Using Co-Precipitation MethodInt J NanomedicineAugust 26, 2026Jiayan Shi, Yueran Wang, Mengting Xu, Shunjie Jin, Ying Yin, Kai He Khor, Xuan Zhou, Ali Bahadur, Kamyar Shameli, Sin-Yeang Teowcytotoxic effect of CuAl LDH was assessed using the CellTiter-Glo luminescent cell viability assay (#G9241, Promega) as previously described.16,17 Briefly, 5 × 103 cells per well (100 μL/well) were seeded onto

(14) Mesoscale proximity labeling at chromatin leads to identification of small molecule mechanism of actionNature CommunicationsAugust 24, 2026Cameron J. Douglas, Preston Samowitz, Feifei Tong, Alice Long, Caitlin M. Bradley, Laszlo Radnai, David W. C. MacMillan, Courtney A. Miller, Gavin Rumbaugh, Ciaran P. Seaththe plates, and 100 µL of a room-temperature mixture of 1:1 DPBS and CellTiter-Glo® 2.0 Reagent (cat. G9242, Promega) was dispensed into each well using a multichannel pipette. Plates were shaken for 2 min at

(15) A host-centric morphological profiling approach to identify repurposed antiviral drugsiScienceAugust 21, 2026Elin Asp, Jonne Rietdijk, Marianna Tampere, Hanna Axelsson, Duncan Njenda, Swapnil Potdar, Adelinn Kalman, Polina Georgieva, Maris Lapins, Flavio Ballante, et al.proteins" ,, SPECs drug repurposing library,https://www.specs.net/,N/A CellTiter-Glo,Promega,Ref. G9243 Paraformaldehyde,Thermo Scientific,Ref. 28908 BSA,Sigma,Ref. A8022 Hoechst 33342,Invitrogen,Ref.

(16) The requirement of MALT1 activity for the growth of adult T cell leukemia/lymphomaiScienceAugust 21, 2026Ayako Kamiunten, Daisuke Morishita, Takuro Kameda, Midori Sugiyama, Shunsuke Ebara, Yasunori Kogure, Akio Mizutani, Takaharu Hirayama, Tomohiro Kawamoto, Yotaro Ochi, et al.commercial assays,Critical commercial assays ,, CellTiter-Glo® 2.0 Cell Viability Assay,Promega,#G9242 SureSelect Custom Kit,Agilent Technologies,N/A QuantiChrom™ Lactate Dehydrogenase Kit,BioAssay Systems,#D2DH-100 Human

(17) TP53 mutation drives unique transcriptional and functional vulnerabilities independent of del(17p) in multiple myelomaiScienceAugust 21, 2026Dimitrios Tsallos, Nemo Ikonen, Juho J. Miettinen, Muntasir Mamun Majumder, Samuli Eldfors, Imre Västrik, Alun Parsons, Minna Suvela, Katie Dunphy, Paul Dowling, et al.Media,Cytiva,Cat# 11778538 Conditioned medium,This paper,– CellTiter-Glo® 2.0 reagent,Promega Corporation,Cat# G9243 Compounds used in this paper are available on Table S7,–,– ,, Critical commercial assays,Critical

(18) Panitumumab-Based EGFR Blockade in SMARCB1-Deficient Renal Medullary Carcinoma: Preclinical Basis and Prospective Clinical ActivityClin Cancer ResAugust 21, 2026Niki M. Zacharias, Eric S. Rupe, Xinyue Chen, Ritesh R. Kotecha, Damian T. Rieke, Bradley A. McGregor, Pedro Pesquera, Zhiyuan Yu, Abha Grover, Najat C. Daw, et al.panitumumab was used as is (saline solution). For IC50 assays, CellTiter-Glo® 2.0 Cell Viability assay (G9241, Promega, Madison, WI, USA) was used to determine IC50 of panitumumab on UOK360 and 786-O cells. For

(19) Mitochondrial profiling across macrophage states reveals inhibition of IL-4/IL-13 reprogramming by the integrated stress responseSci AdvAugust 21, 2026Joan Blanco-Fernandez, Miriam Lisci, Mads M. Foged, Chloé Chapuis, Tim Pflästerer, Tatjana Kleele, Alexis A. Jourdainstimulation, ATP was quantified using the CellTiter-Glo luminescent cell viability assay kit (Promega, G9242) according to the manufacturer’s instructions. Briefly, 100 μl of reconstituted CellTiter-Glo Reagent

(20) Crosstalk between S-nitrosylation and glycation defines a metabolic vulnerability in liver and renal cancersNature CommunicationsAugust 20, 2026Chiara Pecorari, Mojca Bratina, Evelyn Gonzalez, Salvatore Rizza, Letizia Incampo, Lina Vardouli, Paola Giglio, Elena Maresca, Zsófia Márta Sztupinszki, Marcus Montanares Kildegaard Nielsen, et al.48 or 72 h, and viability was quantified using the CellTiter-Glo® 2D Cell Viability Assay (Promega, G9242) following the manufacturer’s instructions. Luminescence was measured using a Victor X4 plate reader

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CellTiter-Glo 2.0 Assay

CellTiter-Glo 2.0 Assay from Promega

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CellTiter-Glo 2.0 Assay from Promega

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