igg2b kappa Search Results


anti cd45  (Novus Biologicals)
93
Novus Biologicals anti cd45
A. Confocal 3D scans showing the monocytes on top of the epithelial barrier, at 72 hours cocultures of ALI epithelia with monocytes. B. Lateral view of the 3D scan showing the monocytes on top of epithelial cells, not passing through the tight junctions. C. Dot-plot illustrating that monocytes can be isolated from cocultures with ALI epithelium by expression of <t>CD45</t> and CD14 D-E. Upon contact with epithelium blood monocytes increased MERTK expression as illustrated MFI of MERTK (D) and by % of MERTK positive cells (E). Each dot represents monocytes from 3 different patients on 3 different ALI epithelial systems (N=3). Statistical analysis was performed using One-Way Anova with Tukey’s multiple comparisons test. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. Data is presented as bar plot +/- SD of mean. F. SARS-Cov-2 Infected bronchial cells produced MCSF and CCL2, but no GM- CSF, at 72 hours. Each group is represented by multiple transwell systems that were used as control or infected with SARS-CoV-2, Mock N= 6, SARS-CoV-2 infected epithelia N= 9. Data is presented as bar plot with +/- SD of mean. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 G. The IFN-β stimulated epithelium did not affect GM-CSF production. IFN-β pre-treated cocultures had lower levels of GM-CSF compared to controls at 72 hours (left graph). IFN-β stimulation resulted in higher M-CSF production from the epithelium at 24 hours. At 72 hour, the cocultures pre-treated with IFN-β also had higher M-CSF levels than the controls (right). Each group is represented by multiple transwell systems that were used as control or stimulated with 10 ng/mL IFN-β (24 hours stimulated cultures N=4, 72 hours cocultures N= 3). Data is presented as bar plot with mean +/- SD. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001
Anti Cd45, supplied by Novus Biologicals, 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/result/anti cd45/product/Novus Biologicals
Average 93 stars, based on 1 article reviews
anti cd45 - by Bioz Stars, 2026-03
93/100 stars
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igg  (MedChemExpress)
94
MedChemExpress igg
A. Confocal 3D scans showing the monocytes on top of the epithelial barrier, at 72 hours cocultures of ALI epithelia with monocytes. B. Lateral view of the 3D scan showing the monocytes on top of epithelial cells, not passing through the tight junctions. C. Dot-plot illustrating that monocytes can be isolated from cocultures with ALI epithelium by expression of <t>CD45</t> and CD14 D-E. Upon contact with epithelium blood monocytes increased MERTK expression as illustrated MFI of MERTK (D) and by % of MERTK positive cells (E). Each dot represents monocytes from 3 different patients on 3 different ALI epithelial systems (N=3). Statistical analysis was performed using One-Way Anova with Tukey’s multiple comparisons test. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. Data is presented as bar plot +/- SD of mean. F. SARS-Cov-2 Infected bronchial cells produced MCSF and CCL2, but no GM- CSF, at 72 hours. Each group is represented by multiple transwell systems that were used as control or infected with SARS-CoV-2, Mock N= 6, SARS-CoV-2 infected epithelia N= 9. Data is presented as bar plot with +/- SD of mean. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 G. The IFN-β stimulated epithelium did not affect GM-CSF production. IFN-β pre-treated cocultures had lower levels of GM-CSF compared to controls at 72 hours (left graph). IFN-β stimulation resulted in higher M-CSF production from the epithelium at 24 hours. At 72 hour, the cocultures pre-treated with IFN-β also had higher M-CSF levels than the controls (right). Each group is represented by multiple transwell systems that were used as control or stimulated with 10 ng/mL IFN-β (24 hours stimulated cultures N=4, 72 hours cocultures N= 3). Data is presented as bar plot with mean +/- SD. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001
Igg, supplied by MedChemExpress, 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/result/igg/product/MedChemExpress
Average 94 stars, based on 1 article reviews
igg - by Bioz Stars, 2026-03
94/100 stars
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mouse igg2b kappa  (Novus Biologicals)
92
Novus Biologicals mouse igg2b kappa
List of primary antibodies used for flow cytometry and confocal microscopy.
Mouse Igg2b Kappa, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse igg2b kappa/product/Novus Biologicals
Average 92 stars, based on 1 article reviews
mouse igg2b kappa - by Bioz Stars, 2026-03
92/100 stars
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percp cy5 5 mouse igg2b percp cy5 5  (Exosome Diagnostics)
86
Exosome Diagnostics percp cy5 5 mouse igg2b percp cy5 5
List of primary antibodies used for flow cytometry and confocal microscopy.
Percp Cy5 5 Mouse Igg2b Percp Cy5 5, 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/result/percp cy5 5 mouse igg2b percp cy5 5/product/Exosome Diagnostics
Average 86 stars, based on 1 article reviews
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mouse igg2b clone id: cb8 antibody  (Crown Bioscience)
90
Crown Bioscience mouse igg2b clone id: cb8 antibody
List of primary antibodies used for flow cytometry and confocal microscopy.
Mouse Igg2b Clone Id: Cb8 Antibody, supplied by Crown Bioscience, 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/result/mouse igg2b clone id: cb8 antibody/product/Crown Bioscience
Average 90 stars, based on 1 article reviews
mouse igg2b clone id: cb8 antibody - by Bioz Stars, 2026-03
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secondary antibody (mouse igg2b kappa light chain) conjugated to alexa-fluor® 488 for the gfap  (Cohesion Biosciences)
90
Cohesion Biosciences secondary antibody (mouse igg2b kappa light chain) conjugated to alexa-fluor® 488 for the gfap
List of primary antibodies used for flow cytometry and confocal microscopy.
Secondary Antibody (Mouse Igg2b Kappa Light Chain) Conjugated To Alexa Fluor® 488 For The Gfap, supplied by Cohesion Biosciences, 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/result/secondary antibody (mouse igg2b kappa light chain) conjugated to alexa-fluor® 488 for the gfap/product/Cohesion Biosciences
Average 90 stars, based on 1 article reviews
secondary antibody (mouse igg2b kappa light chain) conjugated to alexa-fluor® 488 for the gfap - by Bioz Stars, 2026-03
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do-7 igg2b kappa mouse monoclonal antibody  (Signet Testing)
90
Signet Testing do-7 igg2b kappa mouse monoclonal antibody
List of primary antibodies used for flow cytometry and confocal microscopy.
Do 7 Igg2b Kappa Mouse Monoclonal Antibody, supplied by Signet Testing, 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
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Image Search Results


A. Confocal 3D scans showing the monocytes on top of the epithelial barrier, at 72 hours cocultures of ALI epithelia with monocytes. B. Lateral view of the 3D scan showing the monocytes on top of epithelial cells, not passing through the tight junctions. C. Dot-plot illustrating that monocytes can be isolated from cocultures with ALI epithelium by expression of CD45 and CD14 D-E. Upon contact with epithelium blood monocytes increased MERTK expression as illustrated MFI of MERTK (D) and by % of MERTK positive cells (E). Each dot represents monocytes from 3 different patients on 3 different ALI epithelial systems (N=3). Statistical analysis was performed using One-Way Anova with Tukey’s multiple comparisons test. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. Data is presented as bar plot +/- SD of mean. F. SARS-Cov-2 Infected bronchial cells produced MCSF and CCL2, but no GM- CSF, at 72 hours. Each group is represented by multiple transwell systems that were used as control or infected with SARS-CoV-2, Mock N= 6, SARS-CoV-2 infected epithelia N= 9. Data is presented as bar plot with +/- SD of mean. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 G. The IFN-β stimulated epithelium did not affect GM-CSF production. IFN-β pre-treated cocultures had lower levels of GM-CSF compared to controls at 72 hours (left graph). IFN-β stimulation resulted in higher M-CSF production from the epithelium at 24 hours. At 72 hour, the cocultures pre-treated with IFN-β also had higher M-CSF levels than the controls (right). Each group is represented by multiple transwell systems that were used as control or stimulated with 10 ng/mL IFN-β (24 hours stimulated cultures N=4, 72 hours cocultures N= 3). Data is presented as bar plot with mean +/- SD. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Journal: bioRxiv

Article Title: PROS1 released by human lung basal cells upon SARS-CoV-2 infection facilitates epithelial cell repair and limits inflammation

doi: 10.1101/2024.09.11.612489

Figure Lengend Snippet: A. Confocal 3D scans showing the monocytes on top of the epithelial barrier, at 72 hours cocultures of ALI epithelia with monocytes. B. Lateral view of the 3D scan showing the monocytes on top of epithelial cells, not passing through the tight junctions. C. Dot-plot illustrating that monocytes can be isolated from cocultures with ALI epithelium by expression of CD45 and CD14 D-E. Upon contact with epithelium blood monocytes increased MERTK expression as illustrated MFI of MERTK (D) and by % of MERTK positive cells (E). Each dot represents monocytes from 3 different patients on 3 different ALI epithelial systems (N=3). Statistical analysis was performed using One-Way Anova with Tukey’s multiple comparisons test. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001. Data is presented as bar plot +/- SD of mean. F. SARS-Cov-2 Infected bronchial cells produced MCSF and CCL2, but no GM- CSF, at 72 hours. Each group is represented by multiple transwell systems that were used as control or infected with SARS-CoV-2, Mock N= 6, SARS-CoV-2 infected epithelia N= 9. Data is presented as bar plot with +/- SD of mean. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 G. The IFN-β stimulated epithelium did not affect GM-CSF production. IFN-β pre-treated cocultures had lower levels of GM-CSF compared to controls at 72 hours (left graph). IFN-β stimulation resulted in higher M-CSF production from the epithelium at 24 hours. At 72 hour, the cocultures pre-treated with IFN-β also had higher M-CSF levels than the controls (right). Each group is represented by multiple transwell systems that were used as control or stimulated with 10 ng/mL IFN-β (24 hours stimulated cultures N=4, 72 hours cocultures N= 3). Data is presented as bar plot with mean +/- SD. Statistical comparison was performed using unpaired T test between different conditions. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001

Article Snippet: For isotype of anti-CD45, mouse IgG2b was used (Novus-Bio, NBP1-43317), whereas for anti-TJP1, rabbit IgG (Vector Laboratories, I-1000) was used.

Techniques: Isolation, Expressing, Infection, Produced, Control, Comparison

List of primary antibodies used for flow cytometry and confocal microscopy.

Journal: Poultry Science

Article Title: Mesenchymal stem cells of Oravka chicken breed: promising path to biodiversity conservation

doi: 10.1016/j.psj.2023.102807

Figure Lengend Snippet: List of primary antibodies used for flow cytometry and confocal microscopy.

Article Snippet: CD146 , Mouse IgG2b Kappa , c264 , FITC , Novus Biologicals.

Techniques: Flow Cytometry, Microscopy, Purification, Marker