nis-element viewer 4.50 Search Results


niselements viewer 4 50  (Nikon)
99
Nikon niselements viewer 4 50
Niselements Viewer 4 50, supplied by Nikon, 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/nis-element+viewer+4%2E50/NIS-Elements/pm36732771-84-14-17
Average 99 stars, based on 1 article reviews
niselements viewer 4 50 - by Bioz Stars, 2026-09
99/100 stars
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circles  (Carolina Biological)
93
Carolina Biological circles
Circles, supplied by Carolina Biological, 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/nis-element+viewer+4%2E50/Cover+Glasses%2C+Circles%2C+Thickness/pm37777959-241-39-41
Average 93 stars, based on 1 article reviews
circles - by Bioz Stars, 2026-09
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confocal microscope  (Nikon)
96
Nikon confocal microscope
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Confocal Microscope, supplied by Nikon, 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/nis-element+viewer+4%2E50/N-SIM+S/pmc12341598-261-5-11
Average 96 stars, based on 1 article reviews
confocal microscope - by Bioz Stars, 2026-09
96/100 stars
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snapgene software v4.3.4  (GSL Biotech)
90
GSL Biotech snapgene software v4.3.4
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Snapgene Software V4.3.4, supplied by GSL Biotech, 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/nis-element+viewer+4%2E50/snapgene+software/pmc10794148__41586_2023_6889_MOESM1_ESM-24-25-28
Average 90 stars, based on 1 article reviews
snapgene software v4.3.4 - by Bioz Stars, 2026-09
90/100 stars
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lasers  (Nikon)
99
Nikon lasers
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Lasers, supplied by Nikon, 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/nis-element+viewer+4%2E50/Objectives/pmc08529056-74-35-36
Average 99 stars, based on 1 article reviews
lasers - by Bioz Stars, 2026-09
99/100 stars
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a1rs hd confocal microscope system  (Nikon)
99
Nikon a1rs hd confocal microscope system
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
A1rs Hd Confocal Microscope System, supplied by Nikon, 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/nis-element+viewer+4%2E50/ECLIPSE+Ti2/pmc08529056-74-6-5
Average 99 stars, based on 1 article reviews
a1rs hd confocal microscope system - by Bioz Stars, 2026-09
99/100 stars
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pro v 7.0  (SoftMax Inc)
90
SoftMax Inc pro v 7.0
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Pro V 7.0, supplied by SoftMax 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/nis-element+viewer+4%2E50/pro+v7+03+software/pmc10589346__41467_2023_42210_MOESM3_ESM-8-41-41
Average 90 stars, based on 1 article reviews
pro v 7.0 - by Bioz Stars, 2026-09
90/100 stars
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pressure–volume (pv) catheter  (Millar Inc)
90
Millar Inc pressure–volume (pv) catheter
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Pressure–Volume (Pv) Catheter, supplied by Millar 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/nis-element+viewer+4%2E50/pressure+volume+catheter/pmc11725574__41467_2025_55917_MOESM4_ESM-9-61-85
Average 90 stars, based on 1 article reviews
pressure–volume (pv) catheter - by Bioz Stars, 2026-09
90/100 stars
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vevo 3100 echocardiography system  (FUJIFILM VisualSonics Inc)
90
FUJIFILM VisualSonics Inc vevo 3100 echocardiography system
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Vevo 3100 Echocardiography System, supplied by FUJIFILM VisualSonics 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/nis-element+viewer+4%2E50/vevo+2100+system/pmc11725574__41467_2025_55917_MOESM4_ESM-9-69-74
Average 90 stars, based on 1 article reviews
vevo 3100 echocardiography system - by Bioz Stars, 2026-09
90/100 stars
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alexa fluor 488 goat anti mouse igg h l  (Abcam)
99
Abcam alexa fluor 488 goat anti mouse igg h l
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Alexa Fluor 488 Goat Anti Mouse Igg H L, supplied by Abcam, 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/nis-element+viewer+4%2E50/Goat+Anti-Mouse+IgG+H%26L/pmc08425412-46-10-17
Average 99 stars, based on 1 article reviews
alexa fluor 488 goat anti mouse igg h l - by Bioz Stars, 2026-09
99/100 stars
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paper n a pcl eco addgene  (Addgene inc)
96
Addgene inc paper n a pcl eco addgene
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
Paper N A Pcl Eco Addgene, supplied by Addgene inc, 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/nis-element+viewer+4%2E50/pCL-Eco+(Plasmid+%2312371)/pm30581117-248-77-80
Average 96 stars, based on 1 article reviews
paper n a pcl eco addgene - by Bioz Stars, 2026-09
96/100 stars
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l-calc software stemcell #28600  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc l-calc software stemcell #28600
Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto <t>microscope</t> cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.
L Calc Software Stemcell #28600, supplied by STEMCELL Technologies 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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Average 90 stars, based on 1 article reviews
l-calc software stemcell #28600 - by Bioz Stars, 2026-09
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Image Search Results


Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto microscope cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.

Journal: Molecular Therapy Oncology

Article Title: CDCP1-targeting ADC outperforms standard therapies in Ras-mutant pancreatic cancer

doi: 10.1016/j.omton.2025.201024

Figure Lengend Snippet: Internalization of the 2G10 antibody in pancreatic cancer cells (A) Cells were seeded onto microscope cover glasses in a 12-well culture plates: PANC-1 (1 × 10 5 cells), AsPC-1 (2 × 10 5 cells), BxPC-3 (2 × 10 5 cells), and MIA PaCa-2 (0.5 × 10 5 cells). After blocking with a blocker for 30 min, cells were treated for 1 h at 4°C with 2G10 antibody (10 μg/mL) conjugated with the anti-mouse IgG-conjugated Alexa 488 (10 μg/mL). Lysosomes were stained with anti-LAMP-1 for 1 h, and the nuclei were counterstained with DAPI (100 nM) at room temperature. The fluorescent images were captured using a confocal microscope at 60× magnification. The experiments were repeated independently at least three times. (B) Pancreatic cancer cells were pre-incubated with CHX (75 μg/mL) and blocked with Fc blocker for 10 min to inhibit the Fc receptor-mediated internalization. The cells were then incubated in the presence or absence of 2G10 antibody (100 ng/mL) at 4°C or 37°C for 2 h and followed by flow cytometry analysis. The fluorescent signal of the 2G10 antibody/CDCP1 complex on the cell surface decreased after incubation at 37°C.

Article Snippet: Images were captured with a confocal microscope (A1R HD25 N-SIM S, Nikon, Tokyo, Japan) and obtained using NIS-Elements Viewer 4.50 software (Nikon).

Techniques: Microscopy, Blocking Assay, Staining, Incubation, Flow Cytometry