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icam 5 monoclonal antibodies  (R&D Systems)


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    Structured Review

    R&D Systems icam 5 monoclonal antibodies
    Icam 5 Monoclonal Antibodies, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/icam 5 monoclonal antibodies/product/R&D Systems
    Average 93 stars, based on 7 article reviews
    icam 5 monoclonal antibodies - by Bioz Stars, 2026-05
    93/100 stars

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    Santa Cruz Biotechnology icam1 g 5
    Effects of ERN1 chemical inhibitors and ERN1 knockdown on dust extract induction of inflammatory mediator protein levels in Beas2B bronchial epithelial cells. (A–E). Cells were first treated for 1 h with medium alone, 1 μM KIRA6, or 1 μM APY29 prior to incubation with 1% dust extract for 3 h. (F–K). Cells were transfected with 10 nM non‐targeting control siRNA or ERN1 siRNA and treated with 1% dust extract for 24 h. Cellular pro IL1β, <t>ICAM1,</t> and ERN1 protein levels and secreted IL6 and CXCL8 levels were determined by western blotting and ELISA, respectively. Pro IL1β, ICAM1, and ERN1 protein levels were normalized to Actin levels. Representative western blots are shown (A, F). Data shown are mean ± SE ( n = 4–8 for chemical inhibitor experiments and n = 4–5 for siRNA transfection experiments). Statistical significance was analyzed by two‐way ANOVA followed by Sidak's post hoc test for analysis between specific groups (G) and Tukey's post hoc test for analysis between multiple groups (B–E, H–K). * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. C, control; DE, dust extract.
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    Santa Cruz Biotechnology icam 1 g 5
    Effects of ERN1 chemical inhibitors and ERN1 knockdown on dust extract induction of inflammatory mediator protein levels in Beas2B bronchial epithelial cells. (A–E). Cells were first treated for 1 h with medium alone, 1 μM KIRA6, or 1 μM APY29 prior to incubation with 1% dust extract for 3 h. (F–K). Cells were transfected with 10 nM non‐targeting control siRNA or ERN1 siRNA and treated with 1% dust extract for 24 h. Cellular pro IL1β, <t>ICAM1,</t> and ERN1 protein levels and secreted IL6 and CXCL8 levels were determined by western blotting and ELISA, respectively. Pro IL1β, ICAM1, and ERN1 protein levels were normalized to Actin levels. Representative western blots are shown (A, F). Data shown are mean ± SE ( n = 4–8 for chemical inhibitor experiments and n = 4–5 for siRNA transfection experiments). Statistical significance was analyzed by two‐way ANOVA followed by Sidak's post hoc test for analysis between specific groups (G) and Tukey's post hoc test for analysis between multiple groups (B–E, H–K). * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. C, control; DE, dust extract.
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    Effects of ERN1 chemical inhibitors and ERN1 knockdown on dust extract induction of inflammatory mediator protein levels in Beas2B bronchial epithelial cells. (A–E). Cells were first treated for 1 h with medium alone, 1 μM KIRA6, or 1 μM APY29 prior to incubation with 1% dust extract for 3 h. (F–K). Cells were transfected with 10 nM non‐targeting control siRNA or ERN1 siRNA and treated with 1% dust extract for 24 h. Cellular pro IL1β, ICAM1, and ERN1 protein levels and secreted IL6 and CXCL8 levels were determined by western blotting and ELISA, respectively. Pro IL1β, ICAM1, and ERN1 protein levels were normalized to Actin levels. Representative western blots are shown (A, F). Data shown are mean ± SE ( n = 4–8 for chemical inhibitor experiments and n = 4–5 for siRNA transfection experiments). Statistical significance was analyzed by two‐way ANOVA followed by Sidak's post hoc test for analysis between specific groups (G) and Tukey's post hoc test for analysis between multiple groups (B–E, H–K). * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. C, control; DE, dust extract.

    Journal: FASEB BioAdvances

    Article Title: Endoplasmic Reticulum Stress and Unfolded Protein Response Sensor ERN1 Regulates Organic Dust Induction of Lung Inflammation

    doi: 10.1096/fba.2025-00069

    Figure Lengend Snippet: Effects of ERN1 chemical inhibitors and ERN1 knockdown on dust extract induction of inflammatory mediator protein levels in Beas2B bronchial epithelial cells. (A–E). Cells were first treated for 1 h with medium alone, 1 μM KIRA6, or 1 μM APY29 prior to incubation with 1% dust extract for 3 h. (F–K). Cells were transfected with 10 nM non‐targeting control siRNA or ERN1 siRNA and treated with 1% dust extract for 24 h. Cellular pro IL1β, ICAM1, and ERN1 protein levels and secreted IL6 and CXCL8 levels were determined by western blotting and ELISA, respectively. Pro IL1β, ICAM1, and ERN1 protein levels were normalized to Actin levels. Representative western blots are shown (A, F). Data shown are mean ± SE ( n = 4–8 for chemical inhibitor experiments and n = 4–5 for siRNA transfection experiments). Statistical significance was analyzed by two‐way ANOVA followed by Sidak's post hoc test for analysis between specific groups (G) and Tukey's post hoc test for analysis between multiple groups (B–E, H–K). * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001. C, control; DE, dust extract.

    Article Snippet: ICAM1 (G‐5) , 1:1000 , sc‐8439, Santa Cruz Biotechnology, Dallas, TX, USA.

    Techniques: Knockdown, Incubation, Transfection, Control, Western Blot, Enzyme-linked Immunosorbent Assay