ccr7 fitc mab Search Results


90
Thermo Fisher fitc anti-mouse i-e k (14-4-4s) mab
Fitc Anti Mouse I E K (14 4 4s) Mab, supplied by Thermo Fisher, 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/fitc anti-mouse i-e k (14-4-4s) mab/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
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95
R&D Systems anti ccr7 fitc mab
( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and <t>CCR7</t> (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.
Anti Ccr7 Fitc Mab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti ccr7 fitc mab/product/R&D Systems
Average 95 stars, based on 1 article reviews
anti ccr7 fitc mab - by Bioz Stars, 2026-03
95/100 stars
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93
R&D Systems fitc conjugated mouse monoclonal antibody
( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and <t>CCR7</t> (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.
Fitc Conjugated Mouse Monoclonal Antibody, supplied by R&D Systems, 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/fitc conjugated mouse monoclonal antibody/product/R&D Systems
Average 93 stars, based on 1 article reviews
fitc conjugated mouse monoclonal antibody - by Bioz Stars, 2026-03
93/100 stars
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91
R&D Systems fitc conjugated mouse anti human ccr7 mab
( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and <t>CCR7</t> (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.
Fitc Conjugated Mouse Anti Human Ccr7 Mab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fitc conjugated mouse anti human ccr7 mab/product/R&D Systems
Average 91 stars, based on 1 article reviews
fitc conjugated mouse anti human ccr7 mab - by Bioz Stars, 2026-03
91/100 stars
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90
R&D Systems anti–ccr7-fitc mab
( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and <t>CCR7</t> (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.
Anti–Ccr7 Fitc Mab, supplied by R&D Systems, 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/anti–ccr7-fitc mab/product/R&D Systems
Average 90 stars, based on 1 article reviews
anti–ccr7-fitc mab - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

95
R&D Systems ccr7 fitc mab
( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and <t>CCR7</t> (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.
Ccr7 Fitc Mab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/ccr7 fitc mab/product/R&D Systems
Average 95 stars, based on 1 article reviews
ccr7 fitc mab - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier

94
R&D Systems anti ccr7 mab
( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and <t>CCR7</t> (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.
Anti Ccr7 Mab, supplied by R&D Systems, 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/anti ccr7 mab/product/R&D Systems
Average 94 stars, based on 1 article reviews
anti ccr7 mab - by Bioz Stars, 2026-03
94/100 stars
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90
Thermo Fisher anti-cd163 fitc
( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and <t>CCR7</t> (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.
Anti Cd163 Fitc, supplied by Thermo Fisher, 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/anti-cd163 fitc/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
anti-cd163 fitc - by Bioz Stars, 2026-03
90/100 stars
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Image Search Results


( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and CCR7 (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.

Journal: PLoS ONE

Article Title: IRX-2, a Novel Immunotherapeutic, Enhances Functions of Human Dendritic Cells

doi: 10.1371/journal.pone.0047234

Figure Lengend Snippet: ( A ) DC obtained from HNSCC patients were matured for 48 h either with IRX-2 or the conventional maturation cocktail. While conventionally matured DC (white bars) expressed higher levels of CD80, CD83 and CD86 (*, p<0.05), IRX-2 matured DC (black bars) showed higher expression of CD11c, CD40 and CCR7 (*, p<0.05). The data are mean x-fold of MFI ± SEM for cells obtained from 12 different HNSCC patients. ( B ) Representative histograms showing expression of DC markers after maturation with IRX-2 or the conventional cytokine cocktail in DC generated from monocytes of one HNSCC patient. The shaded peaks represent isotype controls. ( C ) Migration of mDC in vitro : Migration assays were performed as described in Materials & Methods using DC generated from peripheral blood monocytes of HNSCC patients. While iDC showed very little migration in response to CCL21, both conventional- and IRX-2-matured DC migrated significantly better. Results are shown as the mean absolute numbers of migrated cells ± SEM obtained from 5 different HNSCC patients.

Article Snippet: Anti-CCR7-FITC mAb was from R&D Systems (Minneapolis, MN).

Techniques: Expressing, Generated, Migration, In Vitro