60541 Search Results


psbbi gfp hygromycin resistant vector  (Addgene inc)
94
Addgene inc psbbi gfp hygromycin resistant vector

Psbbi Gfp Hygromycin Resistant Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/60541/pmc08320529-162-0-4?v=Addgene+inc
Average 94 stars, based on 1 article reviews
psbbi gfp hygromycin resistant vector - by Bioz Stars, 2026-08
94/100 stars
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fcγ chain adcc jurkat  (BPS Bioscience)
93
BPS Bioscience fcγ chain adcc jurkat
DARA-mediated <t>ADCC</t> based on CD16 expressing NK cells. A BCBL-1, GTO, and TY-1 cells were incubated with various concentrations of DARA, and co-cultured with ADCC-indicating <t>Jurkat</t> cells (E:T ratio = 1:5) for 18 h. Luciferase activity was measured. B, C, D, E) CFSE-labeled BCBL-1 cells were treated with IgG1 or DARA, co-cultured with CD16 + NK (N6) or CD16- NK (KHYG-1) cell lines at different E:T ratio for 4 h, and analyzed for dead BCBL-1 (CFSE+Ghost Dye+) cells by flow cytometry. F Up-regulation of CD107a after DARA treatment was analyzed by flow cytometry. G Percentages of CD56+CD107a+ cells after stimulation with DARA (n = 3). Data are presented as mean values ± standard error (SE). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 significant levels
Fcγ Chain Adcc Jurkat, supplied by BPS Bioscience, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/60541/pmc10991639-162-26-30?v=BPS+Bioscience
Average 93 stars, based on 1 article reviews
fcγ chain adcc jurkat - by Bioz Stars, 2026-08
93/100 stars
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pichia stipitis cbs  (ATCC)
90
ATCC pichia stipitis cbs
DARA-mediated <t>ADCC</t> based on CD16 expressing NK cells. A BCBL-1, GTO, and TY-1 cells were incubated with various concentrations of DARA, and co-cultured with ADCC-indicating <t>Jurkat</t> cells (E:T ratio = 1:5) for 18 h. Luciferase activity was measured. B, C, D, E) CFSE-labeled BCBL-1 cells were treated with IgG1 or DARA, co-cultured with CD16 + NK (N6) or CD16- NK (KHYG-1) cell lines at different E:T ratio for 4 h, and analyzed for dead BCBL-1 (CFSE+Ghost Dye+) cells by flow cytometry. F Up-regulation of CD107a after DARA treatment was analyzed by flow cytometry. G Percentages of CD56+CD107a+ cells after stimulation with DARA (n = 3). Data are presented as mean values ± standard error (SE). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 significant levels
Pichia Stipitis Cbs, supplied by ATCC, 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/60541/10__1002_slash_jctb__1828-20-26-22?v=ATCC
Average 90 stars, based on 1 article reviews
pichia stipitis cbs - by Bioz Stars, 2026-08
90/100 stars
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human serpin a3/alpha 1-antichymotrypsin elisa kit (colorimetric)  (Bio-Techne corporation)
91
Bio-Techne corporation human serpin a3/alpha 1-antichymotrypsin elisa kit (colorimetric)
DARA-mediated <t>ADCC</t> based on CD16 expressing NK cells. A BCBL-1, GTO, and TY-1 cells were incubated with various concentrations of DARA, and co-cultured with ADCC-indicating <t>Jurkat</t> cells (E:T ratio = 1:5) for 18 h. Luciferase activity was measured. B, C, D, E) CFSE-labeled BCBL-1 cells were treated with IgG1 or DARA, co-cultured with CD16 + NK (N6) or CD16- NK (KHYG-1) cell lines at different E:T ratio for 4 h, and analyzed for dead BCBL-1 (CFSE+Ghost Dye+) cells by flow cytometry. F Up-regulation of CD107a after DARA treatment was analyzed by flow cytometry. G Percentages of CD56+CD107a+ cells after stimulation with DARA (n = 3). Data are presented as mean values ± standard error (SE). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 significant levels
Human Serpin A3/Alpha 1 Antichymotrypsin Elisa Kit (Colorimetric), supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/60541/bio-techne+corporation___nbp2-60541?v=Bio-Techne+corporation
Average 91 stars, based on 1 article reviews
human serpin a3/alpha 1-antichymotrypsin elisa kit (colorimetric) - by Bioz Stars, 2026-08
91/100 stars
  Buy from Supplier
exp cell res small interfering rna sirna dlg5 sirna  (Santa Cruz Biotechnology)
85
Santa Cruz Biotechnology exp cell res small interfering rna sirna dlg5 sirna
DARA-mediated <t>ADCC</t> based on CD16 expressing NK cells. A BCBL-1, GTO, and TY-1 cells were incubated with various concentrations of DARA, and co-cultured with ADCC-indicating <t>Jurkat</t> cells (E:T ratio = 1:5) for 18 h. Luciferase activity was measured. B, C, D, E) CFSE-labeled BCBL-1 cells were treated with IgG1 or DARA, co-cultured with CD16 + NK (N6) or CD16- NK (KHYG-1) cell lines at different E:T ratio for 4 h, and analyzed for dead BCBL-1 (CFSE+Ghost Dye+) cells by flow cytometry. F Up-regulation of CD107a after DARA treatment was analyzed by flow cytometry. G Percentages of CD56+CD107a+ cells after stimulation with DARA (n = 3). Data are presented as mean values ± standard error (SE). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 significant levels
Exp Cell Res Small Interfering Rna Sirna Dlg5 Sirna, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/60541/pm25478998-58-22-34?v=Santa+Cruz+Biotechnology
Average 85 stars, based on 1 article reviews
exp cell res small interfering rna sirna dlg5 sirna - by Bioz Stars, 2026-08
85/100 stars
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Image Search Results


Journal: Cell

Article Title: Secreted gelsolin inhibits DNGR-1-dependent cross-presentation and cancer immunity

doi: 10.1016/j.cell.2021.05.021

Figure Lengend Snippet:

Article Snippet: pSBbi-GFP-hygromycin resistant vector , Addgene , 605414.

Techniques: Enzyme-linked Immunosorbent Assay, shRNA, Recombinant, Staining, SYBR Green Assay, Cell Isolation, Expressing, Clone Assay, Plasmid Preparation, Software

DARA-mediated ADCC based on CD16 expressing NK cells. A BCBL-1, GTO, and TY-1 cells were incubated with various concentrations of DARA, and co-cultured with ADCC-indicating Jurkat cells (E:T ratio = 1:5) for 18 h. Luciferase activity was measured. B, C, D, E) CFSE-labeled BCBL-1 cells were treated with IgG1 or DARA, co-cultured with CD16 + NK (N6) or CD16- NK (KHYG-1) cell lines at different E:T ratio for 4 h, and analyzed for dead BCBL-1 (CFSE+Ghost Dye+) cells by flow cytometry. F Up-regulation of CD107a after DARA treatment was analyzed by flow cytometry. G Percentages of CD56+CD107a+ cells after stimulation with DARA (n = 3). Data are presented as mean values ± standard error (SE). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 significant levels

Journal: Cancer Immunology, Immunotherapy : CII

Article Title: Efficacy and mechanism of the anti-CD38 monoclonal antibody Daratumumab against primary effusion lymphoma

doi: 10.1007/s00262-021-03054-8

Figure Lengend Snippet: DARA-mediated ADCC based on CD16 expressing NK cells. A BCBL-1, GTO, and TY-1 cells were incubated with various concentrations of DARA, and co-cultured with ADCC-indicating Jurkat cells (E:T ratio = 1:5) for 18 h. Luciferase activity was measured. B, C, D, E) CFSE-labeled BCBL-1 cells were treated with IgG1 or DARA, co-cultured with CD16 + NK (N6) or CD16- NK (KHYG-1) cell lines at different E:T ratio for 4 h, and analyzed for dead BCBL-1 (CFSE+Ghost Dye+) cells by flow cytometry. F Up-regulation of CD107a after DARA treatment was analyzed by flow cytometry. G Percentages of CD56+CD107a+ cells after stimulation with DARA (n = 3). Data are presented as mean values ± standard error (SE). *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001 significant levels

Article Snippet: Recombinant Jurkat T cells expressing firefly luciferase gene under the control of NFAT response elements with constitutive expression of human FcγRIIIa, high affinity (V158) variant and Fcγ chain (ADCC-Jurkat) (#60,541, BPS Bioscience, San Diego, CA) were used to measure ADCC activity by reporter assay.

Techniques: Expressing, Incubation, Cell Culture, Luciferase, Activity Assay, Labeling, Flow Cytometry