aspc-1 Search Results


aspc 1  (ATCC)
99
ATCC aspc 1
Aspc 1, 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/aspc-1/AsPC-1/pm26830354-55-7-17
Average 99 stars, based on 1 article reviews
aspc 1 - by Bioz Stars, 2026-10
99/100 stars
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94
CLS Cell Lines Service GmbH aspc
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc, supplied by CLS Cell Lines Service GmbH, 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/aspc-1/AsPC-1+Cells/bio_rxiv__2025__08__10__669537-182-7-5
Average 94 stars, based on 1 article reviews
aspc - by Bioz Stars, 2026-10
94/100 stars
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96
ATCC human pancreatic adenocarcinoma cell line aspc
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Human Pancreatic Adenocarcinoma Cell Line Aspc, 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/aspc-1/AsPC-1%3B+Pancreatic+Cancer%3B+Human/pmc08144369-178-0-9
Average 96 stars, based on 1 article reviews
human pancreatic adenocarcinoma cell line aspc - by Bioz Stars, 2026-10
96/100 stars
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90
BioResource International Inc aspc-1
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc 1, 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
https://www.bioz.com/product/aspc-1/aspc+1/pm35364561-73-17-26
Average 90 stars, based on 1 article reviews
aspc-1 - by Bioz Stars, 2026-10
90/100 stars
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90
DS Pharma Biomedical human pancreatic cancer cell lines aspc-1
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Human Pancreatic Cancer Cell Lines Aspc 1, supplied by DS Pharma Biomedical, 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/aspc-1/aspc+1/pm18037960-186-7-22
Average 90 stars, based on 1 article reviews
human pancreatic cancer cell lines aspc-1 - by Bioz Stars, 2026-10
90/100 stars
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90
European Collection of Authenticated Cell Cultures aspc-1 human pancreatic carcinoma cells
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc 1 Human Pancreatic Carcinoma Cells, supplied by European Collection of Authenticated Cell Cultures, 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/aspc-1/aspc+1+human+pancreatic+carcinoma+cells/pm32514725-54-2-12
Average 90 stars, based on 1 article reviews
aspc-1 human pancreatic carcinoma cells - by Bioz Stars, 2026-10
90/100 stars
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90
ProQinase GmbH aspc‑1‑luc cells
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc‑1‑Luc Cells, supplied by ProQinase GmbH, 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/aspc-1/aspc+1+luc/pmc05423209-105-19-31
Average 90 stars, based on 1 article reviews
aspc‑1‑luc cells - by Bioz Stars, 2026-10
90/100 stars
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90
JCRB Cell Bank aspc-1 cells stably transfected with a luciferase reporter construct
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc 1 Cells Stably Transfected With A Luciferase Reporter Construct, supplied by JCRB Cell Bank, 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/aspc-1/aspc+1+luc/pmc08881656-279-6-14
Average 90 stars, based on 1 article reviews
aspc-1 cells stably transfected with a luciferase reporter construct - by Bioz Stars, 2026-10
90/100 stars
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90
Shanghai GenePharma aspc-1-gem
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc 1 Gem, supplied by Shanghai GenePharma, 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/aspc-1/aspc+1+gem/pmc06678460-40-26-30
Average 90 stars, based on 1 article reviews
aspc-1-gem - by Bioz Stars, 2026-10
90/100 stars
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90
Changyi Aoxin Chemical Co Ltd human coronary artery endothelial cells
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Human Coronary Artery Endothelial Cells, supplied by Changyi Aoxin Chemical Co Ltd, 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/aspc-1/aspc+1+cells++human+pancreatic+tumor+cell+line++transformed+with+a+gfp+plasmid/10__1161_slash_atvbaha__108__163667-13-8-13
Average 90 stars, based on 1 article reviews
human coronary artery endothelial cells - by Bioz Stars, 2026-10
90/100 stars
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90
iCell Bioscience Inc aspc-1 cells
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc 1 Cells, supplied by iCell Bioscience Inc, 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/aspc-1/aspc+1+++h021+/pm39741300-74-3-8
Average 90 stars, based on 1 article reviews
aspc-1 cells - by Bioz Stars, 2026-10
90/100 stars
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90
Corning Life Sciences aspc-1-lucferase cells
A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging <t>of</t> <t>AsPC-1</t> TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.
Aspc 1 Lucferase Cells, supplied by Corning Life Sciences, 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/aspc-1/aspc+1+lucferase+cells/pmc09391072-78-7-23
Average 90 stars, based on 1 article reviews
aspc-1-lucferase cells - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging of AsPC-1 TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.

Journal: bioRxiv

Article Title: Novel combination of irreversible electroporation and allogenic chimeric antigen receptor (CAR) T-cell therapy synergizes therapeutic outcomes in a preclinical human pancreatic cancer mouse model

doi: 10.1101/2025.08.10.669537

Figure Lengend Snippet: A) In vitro tumor spheroid (TS) assay to assess the treatment response to electroporation and CAR T-cell therapy. (1) TSs were formed within a low-adherent U-bottom 96-well, (2) then moved to a 4-well rectangular plate with low- conductivity buffer to (3) deliver electroporation via parallel plate electrodes. (4) The TSs were immediately moved back into the original U-bottom well, where (5) adjuvant CAR T-cells therapy or sham was delivered. B) Live (green) and dead (red) imaging of AsPC-1 TSs at 3 hours and 72 hours after treatment for different electric field magnitudes; scale bar is 1 mm. Normalized absorbance for the XTT assay at C) 3 hours and D) 72 hours post-treatment at different electric fields; one-way ANOVA with Tukey’s post-test and correction; mean ± SD; n=3. E) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TSs over time across different electric fields. F) Normalized GFP intensity and G) TS area over time; One-way ANOVAs with Tukey’s post hoc between groups on the last timepoints (*p < 0.05, *** p < 0.001, **** p<0.0001); Multiple One-Sample Wilcoxon signed-ranked tests between that timepoint and zero (# p < 0.05); n = 3.

Article Snippet: Pan02 mouse pancreatic cancer cells (Cytion, 300501), AsPC-1 human pancreatic cancer (CRL-1682), and Jurkat immortalized human T-lymphocytes (ATCC, TIB-152) were cultured in RPMI-1640 medium (ThermoFisher, 11875093) supplemented with 10% (v/v) fetal bovine serum (Fisher Scientific, FB12999102) and 1% (v/v) 10,000 U/ml penicillin-streptomycin (Gibco, 16140122).

Techniques: In Vitro, Electroporation, Adjuvant, Imaging, XTT Assay

A) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TS, B) deep-red intensity of cell tracker- stained CAR T-cells, and C) merged image over time for the CAR T-cell only and combinatorial treatment (both). D) Measured TS area and E) normalized eGFP intensity over time; One-way ANOVAs with Tukey’s post hoc between groups on the last time points (*p < 0.05, ** p< 0.01, *** p < 0.001, **** p<0.0001); n ≥ 3. F) Comparison of deep-red intensity within the tumor spheroid over time; Two-tailed T-tests between groups at each timepoint (# p < 0.05, ## p < 0.01), n ≥ 3.

Journal: bioRxiv

Article Title: Novel combination of irreversible electroporation and allogenic chimeric antigen receptor (CAR) T-cell therapy synergizes therapeutic outcomes in a preclinical human pancreatic cancer mouse model

doi: 10.1101/2025.08.10.669537

Figure Lengend Snippet: A) Green fluorescent intensity of FLuc-eGFP + AsPC-1 TS, B) deep-red intensity of cell tracker- stained CAR T-cells, and C) merged image over time for the CAR T-cell only and combinatorial treatment (both). D) Measured TS area and E) normalized eGFP intensity over time; One-way ANOVAs with Tukey’s post hoc between groups on the last time points (*p < 0.05, ** p< 0.01, *** p < 0.001, **** p<0.0001); n ≥ 3. F) Comparison of deep-red intensity within the tumor spheroid over time; Two-tailed T-tests between groups at each timepoint (# p < 0.05, ## p < 0.01), n ≥ 3.

Article Snippet: Pan02 mouse pancreatic cancer cells (Cytion, 300501), AsPC-1 human pancreatic cancer (CRL-1682), and Jurkat immortalized human T-lymphocytes (ATCC, TIB-152) were cultured in RPMI-1640 medium (ThermoFisher, 11875093) supplemented with 10% (v/v) fetal bovine serum (Fisher Scientific, FB12999102) and 1% (v/v) 10,000 U/ml penicillin-streptomycin (Gibco, 16140122).

Techniques: Staining, Comparison, Two Tailed Test