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pe conjugated rat anti mouse cxcr2  (R&D Systems)


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    Structured Review

    R&D Systems pe conjugated rat anti mouse cxcr2
    Pe Conjugated Rat Anti Mouse Cxcr2, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pe+conjugated+rat+anti+mouse+cxcr2/pm27105612-79-7-11?v=R%26D+Systems
    Average 95 stars, based on 3 article reviews
    pe conjugated rat anti mouse cxcr2 - by Bioz Stars, 2026-08
    95/100 stars

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    R&D Systems pe conjugated rat anti mouse cxcr2
    Pe Conjugated Rat Anti Mouse Cxcr2, 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
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    Average 95 stars, based on 1 article reviews
    pe conjugated rat anti mouse cxcr2 - by Bioz Stars, 2026-08
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    R&D Systems phycoerythrin pe conjugated rat monoclonal anti mouse cxcr2
    HPC-7 expressed the main KC and SDF-1α <t>receptors,</t> <t>CXCR2</t> (A) and CXCR4 (B) respectively. Topically treating a healthy kidney with KC [200 ng/ml; C] or SDF-1α [200 ng/ml; D] for 4 hours led to significant HPC-7 recruitment compared to the PBS control. Blocking CXCR2 (E) and CXCR4 (F) on HPC-7 prior to administration also decreased HPC-7 adhesion in vivo within the IR injured kidney. For all figures: PBS controls = solid line; kidney pre-treatments/mAb treated HPC-7 = dashed line. Results are presented as mean ± SEM (n≥4). *p<0.05, **p<0.01.
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    R&D Systems anti mouse cxcr2
    HPC-7 expressed the main KC and SDF-1α <t>receptors,</t> <t>CXCR2</t> (A) and CXCR4 (B) respectively. Topically treating a healthy kidney with KC [200 ng/ml; C] or SDF-1α [200 ng/ml; D] for 4 hours led to significant HPC-7 recruitment compared to the PBS control. Blocking CXCR2 (E) and CXCR4 (F) on HPC-7 prior to administration also decreased HPC-7 adhesion in vivo within the IR injured kidney. For all figures: PBS controls = solid line; kidney pre-treatments/mAb treated HPC-7 = dashed line. Results are presented as mean ± SEM (n≥4). *p<0.05, **p<0.01.
    Anti Mouse Cxcr2, 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
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    Average 93 stars, based on 1 article reviews
    anti mouse cxcr2 - by Bioz Stars, 2026-08
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    R&D Systems anti mouse cxcr2 mab
    HPC-7 expressed the main KC and SDF-1α <t>receptors,</t> <t>CXCR2</t> (A) and CXCR4 (B) respectively. Topically treating a healthy kidney with KC [200 ng/ml; C] or SDF-1α [200 ng/ml; D] for 4 hours led to significant HPC-7 recruitment compared to the PBS control. Blocking CXCR2 (E) and CXCR4 (F) on HPC-7 prior to administration also decreased HPC-7 adhesion in vivo within the IR injured kidney. For all figures: PBS controls = solid line; kidney pre-treatments/mAb treated HPC-7 = dashed line. Results are presented as mean ± SEM (n≥4). *p<0.05, **p<0.01.
    Anti Mouse Cxcr2 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/product/pe+conjugated+rat+anti+mouse+cxcr2/pmc03044910-63-1-7?v=R%26D+Systems
    Average 90 stars, based on 1 article reviews
    anti mouse cxcr2 mab - by Bioz Stars, 2026-08
    90/100 stars
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    HPC-7 expressed the main KC and SDF-1α receptors, CXCR2 (A) and CXCR4 (B) respectively. Topically treating a healthy kidney with KC [200 ng/ml; C] or SDF-1α [200 ng/ml; D] for 4 hours led to significant HPC-7 recruitment compared to the PBS control. Blocking CXCR2 (E) and CXCR4 (F) on HPC-7 prior to administration also decreased HPC-7 adhesion in vivo within the IR injured kidney. For all figures: PBS controls = solid line; kidney pre-treatments/mAb treated HPC-7 = dashed line. Results are presented as mean ± SEM (n≥4). *p<0.05, **p<0.01.

    Journal: PLoS ONE

    Article Title: Modulating the Adhesion of Haematopoietic Stem Cells with Chemokines to Enhance Their Recruitment to the Ischaemically Injured Murine Kidney

    doi: 10.1371/journal.pone.0066489

    Figure Lengend Snippet: HPC-7 expressed the main KC and SDF-1α receptors, CXCR2 (A) and CXCR4 (B) respectively. Topically treating a healthy kidney with KC [200 ng/ml; C] or SDF-1α [200 ng/ml; D] for 4 hours led to significant HPC-7 recruitment compared to the PBS control. Blocking CXCR2 (E) and CXCR4 (F) on HPC-7 prior to administration also decreased HPC-7 adhesion in vivo within the IR injured kidney. For all figures: PBS controls = solid line; kidney pre-treatments/mAb treated HPC-7 = dashed line. Results are presented as mean ± SEM (n≥4). *p<0.05, **p<0.01.

    Article Snippet: Flow cytometry studies were conducted using fluorescein isothiocyanate (FITC)-conjugated isotype control rat IgG2b, phycoerythrin (PE)-conjugated isotype control IgG2b, FITC-anti-CD18 (GAME-46; Santa Cruz), PE-anti-CD44 (IM7), FITC-anti-CD49d (MFR4.B), FITC-CD184 (CXCR4; 2B11; eBioscience, San Diego, California, USA) and Phycoerythrin (PE)-conjugated rat monoclonal anti-mouse CXCR2 (242216; R&D Systems, UK).

    Techniques: Control, Blocking Assay, In Vivo