mouse anti–human cd11a (itgal) Search Results


93
Miltenyi Biotec cd11a
List of antibodies used for the immunological analysis of the DSL-6A/C1 tumors.
Cd11a, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio-Rad anti human lfa 1 ab mca1848
List of antibodies used for the immunological analysis of the DSL-6A/C1 tumors.
Anti Human Lfa 1 Ab Mca1848, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Bio X Cell anti lfa1
List of antibodies used for the immunological analysis of the DSL-6A/C1 tumors.
Anti Lfa1, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cedarlane mouse monoclonal igg2a
Primary antibodies used in this study.
Mouse Monoclonal Igg2a, supplied by Cedarlane, 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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Miltenyi Biotec apc anti human cd11a
Antibodies used for flow cytometry.
Apc Anti Human Cd11a, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson monoclonal mouse anti-human cd11a/lfa-1
Antibodies used for flow cytometry.
Monoclonal Mouse Anti Human Cd11a/Lfa 1, supplied by Becton Dickinson, 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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Becton Dickinson αcd11a
Antibodies used for flow cytometry.
αcd11a, supplied by Becton Dickinson, 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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Bio X Cell cd11a antibody
Loss of Icam1 -mediated homotypic T cell interactions amplifies CD8 T cell expansion and improves effector functions shortly after TCR stimulation (A) Overlapping genes from top 50 hits from each screen, genes are ranked by average effect size. (B) STRING protein-protein interaction analysis of shared targets from the two boxes in (A) (32 genes). Interactions include direct (physical) and indirect (functional) associations. (C) Kaplan-Meier OS curves of patients receiving TIL therapy , (Besser cohort) with high or low ICAM1 expression in TIL products. Significance calculated with regular log rank test. (D) Microscopy images of indicated T cells 24 h after CD3 stimulation (n = 7 biological replicates). (E) Viable Ctrl and Icam1 -KO T cell counts under indicated stimulation conditions as in the screens, analyzed with Mann-Whitney test (n = 4–7 biological replicates). (F) Viable B16.OVA cells after 4 days co-culture with indicated T cells, analyzed with Mann-Whitney test (n = 4 biological replicates). (G) Transcriptomic profiling heatmap of indicated T cells with or without 24 h-CD3 stimulation, showing significantly (p value <0.001) differentially expressed genes ( <xref ref-type=Table S3 ). (H) Proteomic STRING enrichment analysis of differentially expressed proteins comparing Icam1 -KO with Ctrl T cells after 24 h-CD3 stimulation, showing top enriched GO biological process (ranked by enrichment strength (Log 10 (observed/expected)) with FDR < 0.1 ( Table S3 ). (I) Flow cytometry-based cytokine bead array showing cytokines released in the culture medium of indicated T cells after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 7 biological replicates). (J) Viable cell counts of Ctrl or Icam1 -KO T cells ectopically expressing wild type (wt) or mutated ICAM1 (lacking the intracellular domain, dcyt). Cell count was assessed 4 days after CD3 stimulation; analyzed with one-way ANOVA with Holm-Sidak’s multiple comparisons test (n = 3 biological replicates). OE: overexpression. (K) Viable cell counts of Ctrl or ICAM1/2/3 -KO human T cells 1 week after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 5 biological replicates). (L) Viable cell counts of human CD8 cells 1week after CD3 stimulation with or without CD54 (ICAM1) or CD11a (LFA1) blocking antibodies, analyzed with Kruskal-Wallis test with Dunn’s post-hoc test (n = 3 biological replicates). Error bars indicate SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001. " width="250" height="auto" />
Cd11a Antibody, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson cd11a/lfa-1 pe-conjugated mouse antibody clone hi111
Loss of Icam1 -mediated homotypic T cell interactions amplifies CD8 T cell expansion and improves effector functions shortly after TCR stimulation (A) Overlapping genes from top 50 hits from each screen, genes are ranked by average effect size. (B) STRING protein-protein interaction analysis of shared targets from the two boxes in (A) (32 genes). Interactions include direct (physical) and indirect (functional) associations. (C) Kaplan-Meier OS curves of patients receiving TIL therapy , (Besser cohort) with high or low ICAM1 expression in TIL products. Significance calculated with regular log rank test. (D) Microscopy images of indicated T cells 24 h after CD3 stimulation (n = 7 biological replicates). (E) Viable Ctrl and Icam1 -KO T cell counts under indicated stimulation conditions as in the screens, analyzed with Mann-Whitney test (n = 4–7 biological replicates). (F) Viable B16.OVA cells after 4 days co-culture with indicated T cells, analyzed with Mann-Whitney test (n = 4 biological replicates). (G) Transcriptomic profiling heatmap of indicated T cells with or without 24 h-CD3 stimulation, showing significantly (p value <0.001) differentially expressed genes ( <xref ref-type=Table S3 ). (H) Proteomic STRING enrichment analysis of differentially expressed proteins comparing Icam1 -KO with Ctrl T cells after 24 h-CD3 stimulation, showing top enriched GO biological process (ranked by enrichment strength (Log 10 (observed/expected)) with FDR < 0.1 ( Table S3 ). (I) Flow cytometry-based cytokine bead array showing cytokines released in the culture medium of indicated T cells after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 7 biological replicates). (J) Viable cell counts of Ctrl or Icam1 -KO T cells ectopically expressing wild type (wt) or mutated ICAM1 (lacking the intracellular domain, dcyt). Cell count was assessed 4 days after CD3 stimulation; analyzed with one-way ANOVA with Holm-Sidak’s multiple comparisons test (n = 3 biological replicates). OE: overexpression. (K) Viable cell counts of Ctrl or ICAM1/2/3 -KO human T cells 1 week after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 5 biological replicates). (L) Viable cell counts of human CD8 cells 1week after CD3 stimulation with or without CD54 (ICAM1) or CD11a (LFA1) blocking antibodies, analyzed with Kruskal-Wallis test with Dunn’s post-hoc test (n = 3 biological replicates). Error bars indicate SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001. " width="250" height="auto" />
Cd11a/Lfa 1 Pe Conjugated Mouse Antibody Clone Hi111, supplied by Becton Dickinson, 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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Immunotec inc fitc-conjugated mouse anti-human mabs cd11a g25.2
Loss of Icam1 -mediated homotypic T cell interactions amplifies CD8 T cell expansion and improves effector functions shortly after TCR stimulation (A) Overlapping genes from top 50 hits from each screen, genes are ranked by average effect size. (B) STRING protein-protein interaction analysis of shared targets from the two boxes in (A) (32 genes). Interactions include direct (physical) and indirect (functional) associations. (C) Kaplan-Meier OS curves of patients receiving TIL therapy , (Besser cohort) with high or low ICAM1 expression in TIL products. Significance calculated with regular log rank test. (D) Microscopy images of indicated T cells 24 h after CD3 stimulation (n = 7 biological replicates). (E) Viable Ctrl and Icam1 -KO T cell counts under indicated stimulation conditions as in the screens, analyzed with Mann-Whitney test (n = 4–7 biological replicates). (F) Viable B16.OVA cells after 4 days co-culture with indicated T cells, analyzed with Mann-Whitney test (n = 4 biological replicates). (G) Transcriptomic profiling heatmap of indicated T cells with or without 24 h-CD3 stimulation, showing significantly (p value <0.001) differentially expressed genes ( <xref ref-type=Table S3 ). (H) Proteomic STRING enrichment analysis of differentially expressed proteins comparing Icam1 -KO with Ctrl T cells after 24 h-CD3 stimulation, showing top enriched GO biological process (ranked by enrichment strength (Log 10 (observed/expected)) with FDR < 0.1 ( Table S3 ). (I) Flow cytometry-based cytokine bead array showing cytokines released in the culture medium of indicated T cells after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 7 biological replicates). (J) Viable cell counts of Ctrl or Icam1 -KO T cells ectopically expressing wild type (wt) or mutated ICAM1 (lacking the intracellular domain, dcyt). Cell count was assessed 4 days after CD3 stimulation; analyzed with one-way ANOVA with Holm-Sidak’s multiple comparisons test (n = 3 biological replicates). OE: overexpression. (K) Viable cell counts of Ctrl or ICAM1/2/3 -KO human T cells 1 week after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 5 biological replicates). (L) Viable cell counts of human CD8 cells 1week after CD3 stimulation with or without CD54 (ICAM1) or CD11a (LFA1) blocking antibodies, analyzed with Kruskal-Wallis test with Dunn’s post-hoc test (n = 3 biological replicates). Error bars indicate SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001. " width="250" height="auto" />
Fitc Conjugated Mouse Anti Human Mabs Cd11a G25.2, supplied by Immunotec 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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fitc-conjugated mouse anti-human mabs cd11a g25.2 - by Bioz Stars, 2026-09
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Becton Dickinson mouse anti-cd11a pe-cy7 hi111

Mouse Anti Cd11a Pe Cy7 Hi111, supplied by Becton Dickinson, 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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Bio X Cell anti mouse lfa 1a cd11a

Anti Mouse Lfa 1a Cd11a, supplied by Bio X Cell, 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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Image Search Results


List of antibodies used for the immunological analysis of the DSL-6A/C1 tumors.

Journal: Cancers

Article Title: Multiparametric Characterization of the DSL-6A/C1 Pancreatic Cancer Model in Rats

doi: 10.3390/cancers16081535

Figure Lengend Snippet: List of antibodies used for the immunological analysis of the DSL-6A/C1 tumors.

Article Snippet: CD11a , PE , REA596 , Human cell line , Miltenyi , 130-109-171.

Techniques:

Primary antibodies used in this study.

Journal: Channels

Article Title: Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A)

doi: 10.1080/19336950.2017.1401688

Figure Lengend Snippet: Primary antibodies used in this study.

Article Snippet: PKCα , Mouse , Purified Mouse Monoclonal IgG2a , 1:1000 , Cedarlane Labs, Burlington, ON , purified bovine brain PKCα (Clone MC5) , [ ] .

Techniques: Affinity Purification, CRAfT Assay, Purification, Recombinant

Antibodies used for flow cytometry.

Journal: Science Advances

Article Title: The tumor suppressor adenomatous polyposis coli regulates T lymphocyte migration

doi: 10.1126/sciadv.abl5942

Figure Lengend Snippet: Antibodies used for flow cytometry.

Article Snippet: APC anti-human CD11a , Mouse IgG1 , Miltenyi Biotec 130-127-294 , 1:50.

Techniques: Cytometry

Loss of Icam1 -mediated homotypic T cell interactions amplifies CD8 T cell expansion and improves effector functions shortly after TCR stimulation (A) Overlapping genes from top 50 hits from each screen, genes are ranked by average effect size. (B) STRING protein-protein interaction analysis of shared targets from the two boxes in (A) (32 genes). Interactions include direct (physical) and indirect (functional) associations. (C) Kaplan-Meier OS curves of patients receiving TIL therapy , (Besser cohort) with high or low ICAM1 expression in TIL products. Significance calculated with regular log rank test. (D) Microscopy images of indicated T cells 24 h after CD3 stimulation (n = 7 biological replicates). (E) Viable Ctrl and Icam1 -KO T cell counts under indicated stimulation conditions as in the screens, analyzed with Mann-Whitney test (n = 4–7 biological replicates). (F) Viable B16.OVA cells after 4 days co-culture with indicated T cells, analyzed with Mann-Whitney test (n = 4 biological replicates). (G) Transcriptomic profiling heatmap of indicated T cells with or without 24 h-CD3 stimulation, showing significantly (p value <0.001) differentially expressed genes ( <xref ref-type=Table S3 ). (H) Proteomic STRING enrichment analysis of differentially expressed proteins comparing Icam1 -KO with Ctrl T cells after 24 h-CD3 stimulation, showing top enriched GO biological process (ranked by enrichment strength (Log 10 (observed/expected)) with FDR < 0.1 ( Table S3 ). (I) Flow cytometry-based cytokine bead array showing cytokines released in the culture medium of indicated T cells after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 7 biological replicates). (J) Viable cell counts of Ctrl or Icam1 -KO T cells ectopically expressing wild type (wt) or mutated ICAM1 (lacking the intracellular domain, dcyt). Cell count was assessed 4 days after CD3 stimulation; analyzed with one-way ANOVA with Holm-Sidak’s multiple comparisons test (n = 3 biological replicates). OE: overexpression. (K) Viable cell counts of Ctrl or ICAM1/2/3 -KO human T cells 1 week after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 5 biological replicates). (L) Viable cell counts of human CD8 cells 1week after CD3 stimulation with or without CD54 (ICAM1) or CD11a (LFA1) blocking antibodies, analyzed with Kruskal-Wallis test with Dunn’s post-hoc test (n = 3 biological replicates). Error bars indicate SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001. " width="100%" height="100%">

Journal: Cancer Cell

Article Title: Multimodal stimulation screens reveal unique and shared genes limiting T cell fitness

doi: 10.1016/j.ccell.2024.02.016

Figure Lengend Snippet: Loss of Icam1 -mediated homotypic T cell interactions amplifies CD8 T cell expansion and improves effector functions shortly after TCR stimulation (A) Overlapping genes from top 50 hits from each screen, genes are ranked by average effect size. (B) STRING protein-protein interaction analysis of shared targets from the two boxes in (A) (32 genes). Interactions include direct (physical) and indirect (functional) associations. (C) Kaplan-Meier OS curves of patients receiving TIL therapy , (Besser cohort) with high or low ICAM1 expression in TIL products. Significance calculated with regular log rank test. (D) Microscopy images of indicated T cells 24 h after CD3 stimulation (n = 7 biological replicates). (E) Viable Ctrl and Icam1 -KO T cell counts under indicated stimulation conditions as in the screens, analyzed with Mann-Whitney test (n = 4–7 biological replicates). (F) Viable B16.OVA cells after 4 days co-culture with indicated T cells, analyzed with Mann-Whitney test (n = 4 biological replicates). (G) Transcriptomic profiling heatmap of indicated T cells with or without 24 h-CD3 stimulation, showing significantly (p value <0.001) differentially expressed genes ( Table S3 ). (H) Proteomic STRING enrichment analysis of differentially expressed proteins comparing Icam1 -KO with Ctrl T cells after 24 h-CD3 stimulation, showing top enriched GO biological process (ranked by enrichment strength (Log 10 (observed/expected)) with FDR < 0.1 ( Table S3 ). (I) Flow cytometry-based cytokine bead array showing cytokines released in the culture medium of indicated T cells after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 7 biological replicates). (J) Viable cell counts of Ctrl or Icam1 -KO T cells ectopically expressing wild type (wt) or mutated ICAM1 (lacking the intracellular domain, dcyt). Cell count was assessed 4 days after CD3 stimulation; analyzed with one-way ANOVA with Holm-Sidak’s multiple comparisons test (n = 3 biological replicates). OE: overexpression. (K) Viable cell counts of Ctrl or ICAM1/2/3 -KO human T cells 1 week after 24 h-CD3 stimulation, analyzed with Mann-Whitney test (n = 5 biological replicates). (L) Viable cell counts of human CD8 cells 1week after CD3 stimulation with or without CD54 (ICAM1) or CD11a (LFA1) blocking antibodies, analyzed with Kruskal-Wallis test with Dunn’s post-hoc test (n = 3 biological replicates). Error bars indicate SD. ∗ p < 0.05; ∗∗ p < 0.01; ∗∗∗ p < 0.001; ∗∗∗∗ p < 0.0001.

Article Snippet: T cell reactivation was performed in the presence of CD11a antibody (1 μg/ml, clone R7-1, BioXCell), CD54 (1 μg/ml, clone R6-5-D6, BioXCell) antibody, CD178/FasL (10 μg/ml, Clone MFL3 (RUO), BD Pharmingen) or respective isotype controls (1 μg/ml, mouse IgG2a, clone C1.18.4 and mouse IgG1, clone MOPC-21, both BioXCell; 10 μg/ml, Armenian Hamster IgG1, κ, BD Pharmingen).

Techniques: Functional Assay, Expressing, Microscopy, MANN-WHITNEY, Co-Culture Assay, Flow Cytometry, Cell Counting, Over Expression, Blocking Assay

Journal: Cancer Cell

Article Title: Multimodal stimulation screens reveal unique and shared genes limiting T cell fitness

doi: 10.1016/j.ccell.2024.02.016

Figure Lengend Snippet:

Article Snippet: T cell reactivation was performed in the presence of CD11a antibody (1 μg/ml, clone R7-1, BioXCell), CD54 (1 μg/ml, clone R6-5-D6, BioXCell) antibody, CD178/FasL (10 μg/ml, Clone MFL3 (RUO), BD Pharmingen) or respective isotype controls (1 μg/ml, mouse IgG2a, clone C1.18.4 and mouse IgG1, clone MOPC-21, both BioXCell; 10 μg/ml, Armenian Hamster IgG1, κ, BD Pharmingen).

Techniques: Purification, Blocking Assay, Control, Functional Assay, Recombinant, Staining, Cell Culture, Isolation, Binding Assay, CRISPR, Sequencing, RNA Sequencing, Software

Journal: Immunity

Article Title: Complex Autoinflammatory Syndrome Unveils Fundamental Principles of JAK1 Kinase Transcriptional and Biochemical Function

doi: 10.1016/j.immuni.2020.07.006

Figure Lengend Snippet:

Article Snippet: Mouse anti-CD11a PE-Cy7 Clone HI111 , BD Biosciences , Cat No. 561387; RRID: AB_10611572.

Techniques: Recombinant, Molecular Cloning, Blocking Assay, Conjugation Assay, Staining, Western Blot, Lysis, Mutagenesis, Isolation, Luminex, Transfection, Amplification, Software, Variant Assay