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Exosome Diagnostics tumor cell derived exosomes
Tumor Cell Derived Exosomes, supplied by Exosome Diagnostics, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/tumor+cell+derived+exosomes/cell+derived+exosomes+myeloma/pm41950246-262-101-74
Average 86 stars, based on 1 article reviews
tumor cell derived exosomes - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

Activity Assay:

Article Title: Engineering exosomes with iRGD for targeted RNAi therapy against pancreatic cancer mediated by long non-coding RNA PLBD1-AS1.
Article Snippet: .. These data suggest that exosomes can effectively deliver siPLBD1-AS1 into target cells and exert biological effects, with iRGD further improving cellular uptake and enhancing their anticancer activity. analysis of α-SMA, VIM, FAP, and β-actin in PSCs after treatment with tumor cell-derived exosomes (n = 3). (C) ELISA of IL-6, MCP-1, and FN levels in the supernatant of PSCs incubated with tumor cell-derived exosomes (n = 3). (E) ECAR and OCR measurements of PSCs following exosome treatment (n = 3). (F) Intracellular and extracellular lactate levels in PSCs after exosome incubation (n = 3). (G) ALDOA enzyme activity in PSCs treated with tumor cell-derived exosomes (n = 3). (H) Western blot analysis of α-SMA, VIM, FAP, and GAPDH in PSCs incubated with exosomes under low glucose, 2-DG, or ALDOA knockdown conditions (n = 3). (I) ELISA of IL-6, MCP-1, and FN in the supernatant of PSCs treated with exosomes under low glucose, 2-DG, or ALDOA knockdown (n = 3). ..

Enzyme-linked Immunosorbent Assay:

Article Title: Engineering exosomes with iRGD for targeted RNAi therapy against pancreatic cancer mediated by long non-coding RNA PLBD1-AS1.
Article Snippet: .. These data suggest that exosomes can effectively deliver siPLBD1-AS1 into target cells and exert biological effects, with iRGD further improving cellular uptake and enhancing their anticancer activity. analysis of α-SMA, VIM, FAP, and β-actin in PSCs after treatment with tumor cell-derived exosomes (n = 3). (C) ELISA of IL-6, MCP-1, and FN levels in the supernatant of PSCs incubated with tumor cell-derived exosomes (n = 3). (E) ECAR and OCR measurements of PSCs following exosome treatment (n = 3). (F) Intracellular and extracellular lactate levels in PSCs after exosome incubation (n = 3). (G) ALDOA enzyme activity in PSCs treated with tumor cell-derived exosomes (n = 3). (H) Western blot analysis of α-SMA, VIM, FAP, and GAPDH in PSCs incubated with exosomes under low glucose, 2-DG, or ALDOA knockdown conditions (n = 3). (I) ELISA of IL-6, MCP-1, and FN in the supernatant of PSCs treated with exosomes under low glucose, 2-DG, or ALDOA knockdown (n = 3). ..

Incubation:

Article Title: Engineering exosomes with iRGD for targeted RNAi therapy against pancreatic cancer mediated by long non-coding RNA PLBD1-AS1.
Article Snippet: .. These data suggest that exosomes can effectively deliver siPLBD1-AS1 into target cells and exert biological effects, with iRGD further improving cellular uptake and enhancing their anticancer activity. analysis of α-SMA, VIM, FAP, and β-actin in PSCs after treatment with tumor cell-derived exosomes (n = 3). (C) ELISA of IL-6, MCP-1, and FN levels in the supernatant of PSCs incubated with tumor cell-derived exosomes (n = 3). (E) ECAR and OCR measurements of PSCs following exosome treatment (n = 3). (F) Intracellular and extracellular lactate levels in PSCs after exosome incubation (n = 3). (G) ALDOA enzyme activity in PSCs treated with tumor cell-derived exosomes (n = 3). (H) Western blot analysis of α-SMA, VIM, FAP, and GAPDH in PSCs incubated with exosomes under low glucose, 2-DG, or ALDOA knockdown conditions (n = 3). (I) ELISA of IL-6, MCP-1, and FN in the supernatant of PSCs treated with exosomes under low glucose, 2-DG, or ALDOA knockdown (n = 3). ..

Western Blot:

Article Title: Engineering exosomes with iRGD for targeted RNAi therapy against pancreatic cancer mediated by long non-coding RNA PLBD1-AS1.
Article Snippet: .. These data suggest that exosomes can effectively deliver siPLBD1-AS1 into target cells and exert biological effects, with iRGD further improving cellular uptake and enhancing their anticancer activity. analysis of α-SMA, VIM, FAP, and β-actin in PSCs after treatment with tumor cell-derived exosomes (n = 3). (C) ELISA of IL-6, MCP-1, and FN levels in the supernatant of PSCs incubated with tumor cell-derived exosomes (n = 3). (E) ECAR and OCR measurements of PSCs following exosome treatment (n = 3). (F) Intracellular and extracellular lactate levels in PSCs after exosome incubation (n = 3). (G) ALDOA enzyme activity in PSCs treated with tumor cell-derived exosomes (n = 3). (H) Western blot analysis of α-SMA, VIM, FAP, and GAPDH in PSCs incubated with exosomes under low glucose, 2-DG, or ALDOA knockdown conditions (n = 3). (I) ELISA of IL-6, MCP-1, and FN in the supernatant of PSCs treated with exosomes under low glucose, 2-DG, or ALDOA knockdown (n = 3). ..

Knockdown:

Article Title: Engineering exosomes with iRGD for targeted RNAi therapy against pancreatic cancer mediated by long non-coding RNA PLBD1-AS1.
Article Snippet: .. These data suggest that exosomes can effectively deliver siPLBD1-AS1 into target cells and exert biological effects, with iRGD further improving cellular uptake and enhancing their anticancer activity. analysis of α-SMA, VIM, FAP, and β-actin in PSCs after treatment with tumor cell-derived exosomes (n = 3). (C) ELISA of IL-6, MCP-1, and FN levels in the supernatant of PSCs incubated with tumor cell-derived exosomes (n = 3). (E) ECAR and OCR measurements of PSCs following exosome treatment (n = 3). (F) Intracellular and extracellular lactate levels in PSCs after exosome incubation (n = 3). (G) ALDOA enzyme activity in PSCs treated with tumor cell-derived exosomes (n = 3). (H) Western blot analysis of α-SMA, VIM, FAP, and GAPDH in PSCs incubated with exosomes under low glucose, 2-DG, or ALDOA knockdown conditions (n = 3). (I) ELISA of IL-6, MCP-1, and FN in the supernatant of PSCs treated with exosomes under low glucose, 2-DG, or ALDOA knockdown (n = 3). ..



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a Trends of publications and major discoveries regarding <t>exosomes.</t> b Publication trends <t>in</t> <t>Exosome</t> research field from 1989 to 2019 (red dotted line: the prediction trends, blue line: the original trends). (Adapted from Reference and respectively under open access article distributed under the Creative Commons Attribution License)
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a Trends of publications and major discoveries regarding exosomes. b Publication trends in Exosome research field from 1989 to 2019 (red dotted line: the prediction trends, blue line: the original trends). (Adapted from Reference and respectively under open access article distributed under the Creative Commons Attribution License)

Journal: Journal of Nanobiotechnology

Article Title: A systematic review on the modifications of extracellular vesicles: a revolutionized tool of nano-biotechnology

doi: 10.1186/s12951-021-01219-2

Figure Lengend Snippet: a Trends of publications and major discoveries regarding exosomes. b Publication trends in Exosome research field from 1989 to 2019 (red dotted line: the prediction trends, blue line: the original trends). (Adapted from Reference and respectively under open access article distributed under the Creative Commons Attribution License)

Article Snippet: 30 , Exosome-based tumor antigens adjuvant co-delivery utilizing genetically engineered tumor cell-derived exosomes with immunostimulatoryCpG DNA , Morishita M, Takahashi Y, Matsumoto A, Nishikawa M, Takakura Y , Japan , 2016 , Genetic Engineering , [ ] .

Techniques:

Summary of characteristics of included studies

Journal: Journal of Nanobiotechnology

Article Title: A systematic review on the modifications of extracellular vesicles: a revolutionized tool of nano-biotechnology

doi: 10.1186/s12951-021-01219-2

Figure Lengend Snippet: Summary of characteristics of included studies

Article Snippet: 30 , Exosome-based tumor antigens adjuvant co-delivery utilizing genetically engineered tumor cell-derived exosomes with immunostimulatoryCpG DNA , Morishita M, Takahashi Y, Matsumoto A, Nishikawa M, Takakura Y , Japan , 2016 , Genetic Engineering , [ ] .

Techniques: In Situ, Fluorescence, Labeling, In Vitro, In Vivo, Synthesized, Conjugation Assay, Cell Culture, Enzyme-linked Immunosorbent Assay, Surround Optical-fiber Immunoassay, Derivative Assay, Functional Assay, Small Interfering RNA, Transfection, CRISPR, Electroporation, Construct, Activity Assay, Sonication, Injection, Binding Assay

Modifications of extracellular vesicles and its role in nano-biotechnology

Journal: Journal of Nanobiotechnology

Article Title: A systematic review on the modifications of extracellular vesicles: a revolutionized tool of nano-biotechnology

doi: 10.1186/s12951-021-01219-2

Figure Lengend Snippet: Modifications of extracellular vesicles and its role in nano-biotechnology

Article Snippet: 30 , Exosome-based tumor antigens adjuvant co-delivery utilizing genetically engineered tumor cell-derived exosomes with immunostimulatoryCpG DNA , Morishita M, Takahashi Y, Matsumoto A, Nishikawa M, Takakura Y , Japan , 2016 , Genetic Engineering , [ ] .

Techniques: Modification, In Vivo, Sonication, Electroporation, Inhibition, Activation Assay