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Promega
cell-based luciferase reporter gene assay ![]() Cell Based Luciferase Reporter Gene Assay, 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/result/cell-based luciferase reporter gene assay/product/Promega Average 90 stars, based on 1 article reviews
cell-based luciferase reporter gene assay - by Bioz Stars,
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Xenova Group
cell-based luciferase reporter gene systems ![]() Cell Based Luciferase Reporter Gene Systems, supplied by Xenova Group, 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/result/cell-based luciferase reporter gene systems/product/Xenova Group Average 90 stars, based on 1 article reviews
cell-based luciferase reporter gene systems - by Bioz Stars,
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Biomonitor
cell-based assay consisting of erythroleukaemic k562 cells transfected with a nfκb-regulated firefly luciferase reporter–gene construct ![]() Cell Based Assay Consisting Of Erythroleukaemic K562 Cells Transfected With A Nfκb Regulated Firefly Luciferase Reporter–Gene Construct, supplied by Biomonitor, 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/result/cell-based assay consisting of erythroleukaemic k562 cells transfected with a nfκb-regulated firefly luciferase reporter–gene construct/product/Biomonitor Average 90 stars, based on 1 article reviews
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Image Search Results
Journal: Antibody Therapeutics
Article Title: Development of a reporter gene method to measure the bioactivity of anti-CD38 × CD3 bispecific antibody
doi: 10.1093/abt/tbab022
Figure Lengend Snippet: The Y150-dependence of gene activation of Jurkat cells: in presence of Jurkat-CD3-NFAT-RE-Luc cells only (in Green), or in presence of Jurkat-CD38 − -CD3-NFAT-RE-Luc cells only (Jurkat-4-3-F11, in Brown), or in presence of both Jurkat-CD3-NFAT-RE-Luc cells and NCI-H929 cells (in Red), or in presence of both Jurkat- CD38 − -CD3-NFAT-RE-Luc cells and NCI-H929 cells (in Blue). In the reporter gene assay, Jurkat cells (effector cells) and NCI-H929 (target cells) were in a ratio of 1.5:1 (E:T).
Article Snippet:
Techniques: Activation Assay, Reporter Gene Assay
Journal: Antibody Therapeutics
Article Title: Development of a reporter gene method to measure the bioactivity of anti-CD38 × CD3 bispecific antibody
doi: 10.1093/abt/tbab022
Figure Lengend Snippet: Validation of reporter gene assay. (A) Specificity assessment of the assay. Y150 or a nonspecific antibody was incubated with both NCI-H929 cells and Jurkat T cell line 4-3-F11, and the RLU signals were measured. Y150 sample stressed under oxidization with 4% hydrogen peroxide was tested and compared with Y150 reference sample. (B) Analysis of linearity of the assay was conducted by comparing the measured potency and expected potency. Each point represents the mean of six independent experiments.
Article Snippet:
Techniques: Reporter Gene Assay, Incubation
Journal: Antibody Therapeutics
Article Title: Development of a reporter gene method to measure the bioactivity of anti-CD38 × CD3 bispecific antibody
doi: 10.1093/abt/tbab022
Figure Lengend Snippet: The correlations of reporter gene assay results with those from cytotoxicity assay and sandwich ELISA assay
Article Snippet:
Techniques: Reporter Gene Assay, Cytotoxicity Assay, Sandwich ELISA