igg1 vector Search Results


95
InvivoGen pfusess-chig-hg1
Pfusess Chig Hg1, supplied by InvivoGen, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
Lonza chok1sv igg1 fc fusion protein
Chok1sv Igg1 Fc Fusion Protein, supplied by Lonza, 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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Average 96 stars, based on 1 article reviews
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90
IDEC Pharmaceuticals Corporation anti-cd23 antibody of the igg1 isotype
Anti Cd23 Antibody Of The Igg1 Isotype, supplied by IDEC Pharmaceuticals Corporation, 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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90
Twist Bioscience igg1 constant fc region 41-98 uniprot: ighg1_human
Igg1 Constant Fc Region 41 98 Uniprot: Ighg1 Human, supplied by Twist Bioscience, 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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90
Crucell Inc igg1, gbs iii-biotin-labelled igg1 antibody
Reactivity and specificity of the human anti-CD1A monoclonal antibodies (mAbs) on different CD1 antigens expressed in the C1R and B16 cell lines. C1R cells expressing either CD1A, CD1B, CD1C or CD1D or no CD1 antigens (termed C1R mock) as well as B16 cells transfected with a viral expression vector containing the cDNA encoding CD1A or empty vector were stained with either CR2113, CR2114, CR2115, CR2116, CR2117 or CR2118 mAbs at 1, 3, and 10 μg/ml. Data for 10 μg mAb/ml are shown and representative of all three doses. Mouse <t>IgG1,</t> κ-FITC was used as a secondary antibody. Cells were analysed by flow cytometry using Kolmogorov-Smirnov statistics to quantitate binding as described in Methods. Specificity was determined by the level of binding to cells expressing specific CD1 isoforms compared to background, isotype control antibody staining. Statistical significance was determined by t-test (unpaired, two-tailed) analysis when comparing the binding of specific monoclonal antibodies to background staining assessed by antibody isotype control staining on cells expressing specific CD1 isoforms. Error bars represent standard deviations. CR2113, CR2114, CR2117 and CR2118 mAbs showed significant binding to CD1A expressing cells with CR2113 having the strongest specific binding characteristics. CR2114 and CR2117 also showed some affinity for CD1C. Legend: ***: p< 0.001, **: p< 0.01, *: p<0.05, ns: p>0.05
Igg1, Gbs Iii Biotin Labelled Igg1 Antibody, supplied by Crucell 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/result/igg1, gbs iii-biotin-labelled igg1 antibody/product/Crucell Inc
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90
AERES Biomedical Ltd vector containing constant region human igg1 chain
Reactivity and specificity of the human anti-CD1A monoclonal antibodies (mAbs) on different CD1 antigens expressed in the C1R and B16 cell lines. C1R cells expressing either CD1A, CD1B, CD1C or CD1D or no CD1 antigens (termed C1R mock) as well as B16 cells transfected with a viral expression vector containing the cDNA encoding CD1A or empty vector were stained with either CR2113, CR2114, CR2115, CR2116, CR2117 or CR2118 mAbs at 1, 3, and 10 μg/ml. Data for 10 μg mAb/ml are shown and representative of all three doses. Mouse <t>IgG1,</t> κ-FITC was used as a secondary antibody. Cells were analysed by flow cytometry using Kolmogorov-Smirnov statistics to quantitate binding as described in Methods. Specificity was determined by the level of binding to cells expressing specific CD1 isoforms compared to background, isotype control antibody staining. Statistical significance was determined by t-test (unpaired, two-tailed) analysis when comparing the binding of specific monoclonal antibodies to background staining assessed by antibody isotype control staining on cells expressing specific CD1 isoforms. Error bars represent standard deviations. CR2113, CR2114, CR2117 and CR2118 mAbs showed significant binding to CD1A expressing cells with CR2113 having the strongest specific binding characteristics. CR2114 and CR2117 also showed some affinity for CD1C. Legend: ***: p< 0.001, **: p< 0.01, *: p<0.05, ns: p>0.05
Vector Containing Constant Region Human Igg1 Chain, supplied by AERES Biomedical Ltd, 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
vector containing constant region human igg1 chain - by Bioz Stars, 2026-03
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Image Search Results


Reactivity and specificity of the human anti-CD1A monoclonal antibodies (mAbs) on different CD1 antigens expressed in the C1R and B16 cell lines. C1R cells expressing either CD1A, CD1B, CD1C or CD1D or no CD1 antigens (termed C1R mock) as well as B16 cells transfected with a viral expression vector containing the cDNA encoding CD1A or empty vector were stained with either CR2113, CR2114, CR2115, CR2116, CR2117 or CR2118 mAbs at 1, 3, and 10 μg/ml. Data for 10 μg mAb/ml are shown and representative of all three doses. Mouse IgG1, κ-FITC was used as a secondary antibody. Cells were analysed by flow cytometry using Kolmogorov-Smirnov statistics to quantitate binding as described in Methods. Specificity was determined by the level of binding to cells expressing specific CD1 isoforms compared to background, isotype control antibody staining. Statistical significance was determined by t-test (unpaired, two-tailed) analysis when comparing the binding of specific monoclonal antibodies to background staining assessed by antibody isotype control staining on cells expressing specific CD1 isoforms. Error bars represent standard deviations. CR2113, CR2114, CR2117 and CR2118 mAbs showed significant binding to CD1A expressing cells with CR2113 having the strongest specific binding characteristics. CR2114 and CR2117 also showed some affinity for CD1C. Legend: ***: p< 0.001, **: p< 0.01, *: p<0.05, ns: p>0.05

Journal: British journal of haematology

Article Title: Phage display generation of a novel human anti-CD1A monoclonal antibody with potent cytolytic activity

doi: 10.1111/bjh.12033

Figure Lengend Snippet: Reactivity and specificity of the human anti-CD1A monoclonal antibodies (mAbs) on different CD1 antigens expressed in the C1R and B16 cell lines. C1R cells expressing either CD1A, CD1B, CD1C or CD1D or no CD1 antigens (termed C1R mock) as well as B16 cells transfected with a viral expression vector containing the cDNA encoding CD1A or empty vector were stained with either CR2113, CR2114, CR2115, CR2116, CR2117 or CR2118 mAbs at 1, 3, and 10 μg/ml. Data for 10 μg mAb/ml are shown and representative of all three doses. Mouse IgG1, κ-FITC was used as a secondary antibody. Cells were analysed by flow cytometry using Kolmogorov-Smirnov statistics to quantitate binding as described in Methods. Specificity was determined by the level of binding to cells expressing specific CD1 isoforms compared to background, isotype control antibody staining. Statistical significance was determined by t-test (unpaired, two-tailed) analysis when comparing the binding of specific monoclonal antibodies to background staining assessed by antibody isotype control staining on cells expressing specific CD1 isoforms. Error bars represent standard deviations. CR2113, CR2114, CR2117 and CR2118 mAbs showed significant binding to CD1A expressing cells with CR2113 having the strongest specific binding characteristics. CR2114 and CR2117 also showed some affinity for CD1C. Legend: ***: p< 0.001, **: p< 0.01, *: p<0.05, ns: p>0.05

Article Snippet: Isotype control antibodies included mAb CR2027, IgG1, GBS III-biotin-labelled IgG1 (Crucell Holland BV, Leiden, The Netherlands), purified mouse IgG2a, κ (BD Biosciences, San Diego, CA), and human IgG1 (Lampire Biological Laboratories, Pipersville, PA, USA) Biotinylation of mAbs Monoclonal antibodies CR2113, CR2114, CR2115, CR2116, CR2117, CR2118 and NA1/34 were incubated with 1M NaHCO 3 and EZ-link Sulfo-NHS-SS-biotin, according to manufacturer’s instruction (Pierce, Rockford, IL, USA).

Techniques: Expressing, Transfection, Plasmid Preparation, Staining, Flow Cytometry, Binding Assay, Two Tailed Test