human cxcr1 Search Results


  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 93
    R&D Systems cxcr2
    IL-8 serves as a survival factor in NU cells. A : urothelial cells transfected with control siRNA remained viable. B : after IL-8 siRNA transfection, urotheial cells round up and die. C : Toluidine blue O staining was used to monitor NU cell numbers after IL-8 siRNA transfection with or without the addition of rIL-8, anti-CXCR1, or <t>CXCR2</t> antibody. The addition of rIL-8 rescued cells after IL-8 siRNA treatment. This rIL-8 rescue effect could be blocked by the addition of anti-CXCR1 but not anti-CXCR2 antibody. Differences that are statistically significant are indicated by *( P
    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
    https://www.bioz.com/result/cxcr2/product/R&D Systems
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    cxcr2 - by Bioz Stars, 2021-09
    93/100 stars
      Buy from Supplier

    cxcr2  (Abcam)
    93
    Abcam cxcr2
    Mouse lung staining for CXCR1 (A,C,E,G) and <t>CXCR2</t> (B,D,F,H). Both receptors were clearly expressed in alveolar epithelium, bronchial epithelium, and alveolar macrophages. Levels of both receptors in Saline (A,B) appeared reduced in G31P treated animals
    Cxcr2, supplied by Abcam, 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/cxcr2/product/Abcam
    Average 93 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    cxcr2 - by Bioz Stars, 2021-09
    93/100 stars
      Buy from Supplier

    91
    R&D Systems anti cxcr2
    Mouse lung staining for CXCR1 (A,C,E,G) and <t>CXCR2</t> (B,D,F,H). Both receptors were clearly expressed in alveolar epithelium, bronchial epithelium, and alveolar macrophages. Levels of both receptors in Saline (A,B) appeared reduced in G31P treated animals
    Anti Cxcr2, 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/anti cxcr2/product/R&D Systems
    Average 91 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti cxcr2 - by Bioz Stars, 2021-09
    91/100 stars
      Buy from Supplier

    92
    R&D Systems anti il 8 antibody
    Neutrophil elastase (NE) degrades TNF, IL-6, and <t>IL-8</t> (A) . THP-1-derived macrophages were exposed to hNE (125–500 mU/mL) in the presence or absence of HK-Spn or LPS (100 ng/mL) for 4 h. TNF, IL-6, and IL-8 concentrations in the culture supernatants were determined by ELISA. Data represent the mean ± SD of quadruplicate experiments and were evaluated using one-way analysis of variance with Tukey’s multiple-comparisons test. *Significantly different within the same activation status at P
    Anti Il 8 Antibody, supplied by R&D Systems, 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/anti il 8 antibody/product/R&D Systems
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti il 8 antibody - by Bioz Stars, 2021-09
    92/100 stars
      Buy from Supplier

    Image Search Results


    IL-8 serves as a survival factor in NU cells. A : urothelial cells transfected with control siRNA remained viable. B : after IL-8 siRNA transfection, urotheial cells round up and die. C : Toluidine blue O staining was used to monitor NU cell numbers after IL-8 siRNA transfection with or without the addition of rIL-8, anti-CXCR1, or CXCR2 antibody. The addition of rIL-8 rescued cells after IL-8 siRNA treatment. This rIL-8 rescue effect could be blocked by the addition of anti-CXCR1 but not anti-CXCR2 antibody. Differences that are statistically significant are indicated by *( P

    Journal: American Journal of Physiology - Renal Physiology

    Article Title: Interleukin-8 is essential for normal urothelial cell survival

    doi: 10.1152/ajprenal.90733.2008

    Figure Lengend Snippet: IL-8 serves as a survival factor in NU cells. A : urothelial cells transfected with control siRNA remained viable. B : after IL-8 siRNA transfection, urotheial cells round up and die. C : Toluidine blue O staining was used to monitor NU cell numbers after IL-8 siRNA transfection with or without the addition of rIL-8, anti-CXCR1, or CXCR2 antibody. The addition of rIL-8 rescued cells after IL-8 siRNA treatment. This rIL-8 rescue effect could be blocked by the addition of anti-CXCR1 but not anti-CXCR2 antibody. Differences that are statistically significant are indicated by *( P

    Article Snippet: Expression of CXCR2 was detected in a subpopulation of normal urothelial cells, but no change, either in the number of positive cells or in the strength of staining, was observed after siRNA transfection with either control or IL-8 siRNA (data not shown).

    Techniques: Transfection, Staining

    Mouse lung staining for CXCR1 (A,C,E,G) and CXCR2 (B,D,F,H). Both receptors were clearly expressed in alveolar epithelium, bronchial epithelium, and alveolar macrophages. Levels of both receptors in Saline (A,B) appeared reduced in G31P treated animals

    Journal: Pulmonary pharmacology & therapeutics

    Article Title: CXCR1/CXCR2 antagonist CXCL8(3-74)K11R/G31P blocks lung inflammation in swine barn dust-instilled mice

    doi: 10.1016/j.pupt.2015.02.002

    Figure Lengend Snippet: Mouse lung staining for CXCR1 (A,C,E,G) and CXCR2 (B,D,F,H). Both receptors were clearly expressed in alveolar epithelium, bronchial epithelium, and alveolar macrophages. Levels of both receptors in Saline (A,B) appeared reduced in G31P treated animals

    Article Snippet: Differential Modes of Regulation of CXC Chemokine-Induced Internalization and Recycling of Human CXCR1 and CXCR2.

    Techniques: Staining

    Neutrophil elastase (NE) degrades TNF, IL-6, and IL-8 (A) . THP-1-derived macrophages were exposed to hNE (125–500 mU/mL) in the presence or absence of HK-Spn or LPS (100 ng/mL) for 4 h. TNF, IL-6, and IL-8 concentrations in the culture supernatants were determined by ELISA. Data represent the mean ± SD of quadruplicate experiments and were evaluated using one-way analysis of variance with Tukey’s multiple-comparisons test. *Significantly different within the same activation status at P

    Journal: Frontiers in Immunology

    Article Title: Neutrophil Elastase Subverts the Immune Response by Cleaving Toll-Like Receptors and Cytokines in Pneumococcal Pneumonia

    doi: 10.3389/fimmu.2018.00732

    Figure Lengend Snippet: Neutrophil elastase (NE) degrades TNF, IL-6, and IL-8 (A) . THP-1-derived macrophages were exposed to hNE (125–500 mU/mL) in the presence or absence of HK-Spn or LPS (100 ng/mL) for 4 h. TNF, IL-6, and IL-8 concentrations in the culture supernatants were determined by ELISA. Data represent the mean ± SD of quadruplicate experiments and were evaluated using one-way analysis of variance with Tukey’s multiple-comparisons test. *Significantly different within the same activation status at P

    Article Snippet: The membrane was probed with an anti-TLR2 antibody (Rockland Immunochemicals, Limerick, PA, USA), anti-TLR4 antibody (Novus Biologicals, Littleton, CO, USA), anti-MD2 antibody (Abcam), anti-NF-κB antibody (Santa Cruz Biotechnology), anti-GAPDH antibody (Abcam), anti-TNF antibody (Cell Signaling Technology, Beverly, MA, USA), anti-IL-6-antibody (Abcam), or anti-IL-8 antibody (R & D Systems) and then incubated with a HRP-conjugated secondary antibody (Cell Signaling Technology) in Tris-buffered saline containing 0.05% tween 20.

    Techniques: Derivative Assay, Enzyme-linked Immunosorbent Assay, Activation Assay