human natural killer cell nk 92mi Search Results


96
ATCC nk 92mi
Nk 92mi, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
Procell Inc human nk cell line nk 92mi
ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in <t>NK</t> <t>cell</t> lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).
Human Nk Cell Line Nk 92mi, supplied by Procell Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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crl  (DSMZ)
96
DSMZ crl
ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in <t>NK</t> <t>cell</t> lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).
Crl, supplied by DSMZ, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+natural+killer+cell+nk+92mi/K-562/pm39561763-206-254-265
Average 96 stars, based on 1 article reviews
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ATCC nk 92 mi
ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in <t>NK</t> <t>cell</t> lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).
Nk 92 Mi, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+natural+killer+cell+nk+92mi/NK-92/pm39235531-26-19-32
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96
ATCC human nk cell line
ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in <t>NK</t> <t>cell</t> lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).
Human Nk Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+natural+killer+cell+nk+92mi/NK-92+%3B+Natural+Killer+Cell%3B+Human+(Homo+sapiens)%3BNK-92+is+a+registered%3B+trademark+of+Nantkwest%2C+Inc/pmc05744589-280-1-6
Average 96 stars, based on 1 article reviews
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90
BioResource International Inc human nk-92mi cell line
ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in <t>NK</t> <t>cell</t> lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).
Human Nk 92mi Cell Line, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
ATCC human nk 92mi natural killer cells
ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in <t>NK</t> <t>cell</t> lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).
Human Nk 92mi Natural Killer Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+natural+killer+cell+nk+92mi/HPAF-II/pm22727646-41-0-17
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N/A
Goat anti-HOXA5 (aa83-92) middle region Antibody (OAEB03190)
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Image Search Results


ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in NK cell lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).

Journal: Journal of Extracellular Vesicles

Article Title: NK Cell‐Derived Small Extracellular Vesicles Armed With CLDN4‐Targeting Peptides Potentiate Radiotherapy in Gastric Cancer

doi: 10.1002/jev2.70200

Figure Lengend Snippet: ROS induction and radiosensitising effects of NESC in NCI‐N87 cells. (a) Western blot analysis of perforin, granzyme B and FasL in NK cell lysate and NK‐sEV. (b) Cell viability of NCI‐N87 cells incubated with three concentrations of NK‐sEVs or NESC (5, 10 and 20 µg). Viability of PBS‐treated cells was considered as a base value. Data was shown as mean ± s.d. ( n = 3). (c) Bar plot showing the KEGG enrichment analysis results, including the pathway names, related genes and pathway classifications. (d and f) Confocal images (f) and quantified data (d) of ROS generation in NCI‐N87 cells treated with different regimens. (blue: DAPI, green: DCFH‐DA). (e and g) Confocal images (g) and quantified data (e) of DNA breaks in NCI‐N87 cells treated with different regimens. (blue: DAPI, red: γ‐H2AX). G1: PBS, G2: NESC (200 µg/mL), G3: 2 Gy and G4: NESC (200 µg/mL) + 2 Gy. p values were calculated by an unpaired t ‐test (* p < 0.05, ** p < 0.01).

Article Snippet: Human NK cell line NK‐92MI, human GC cell lines AGS, MGC803, MKN45, NCI‐N87, SGC7901, SNU‐1 and normal human gastric epithelial cell line GES‐1 were purchased from Procell Life Science & Technology Co., Ltd. (Wuhan, China).

Techniques: Western Blot, Incubation