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rabbit polyclonal anti human fpr3 antibody  (Biorbyt)


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    Structured Review

    Biorbyt rabbit polyclonal anti human fpr3 antibody
    (A) PPI network was constructed basing on the top 300 DEGs. The red icons represent up-regulated genes and the blue ones represent down-regulated genes. Furthermore, the connecting lines between the icons indicate potential interaction between different DEGs. (B) Module analysis of the DEGs enrolled in PPI network using MCODE method. The top five ranking clusters are shown according to MCODE score. (C) Functional enrichment analysis of genes in cluster 1. Likewise, the y axis and x axis represent enrichment terms and scores, respectively, and the color means p- value. (D) The top 10 hub genes are identified from PPI network using MCC method. The color represents MCC score. A darker red icon means higher MCC score and a lighter yellow one represents lower MCC score. (E) mRNA expression levels of CCL13, CCR2, <t>FPR3</t> and PLAU in alveolar macrophages isolated from better prognosis subjects (VFDs > 12) and from poor prognosis individuals (VFDs <12).
    Rabbit Polyclonal Anti Human Fpr3 Antibody, supplied by Biorbyt, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+human+fpr3+antibody/FPR3+antibody/pmc08555499-112-0-6
    Average 92 stars, based on 4 article reviews
    rabbit polyclonal anti human fpr3 antibody - by Bioz Stars, 2026-10
    92/100 stars

    Images

    1) Product Images from "Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome"

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome

    Journal: PeerJ

    doi: 10.7717/peerj.12312

    (A) PPI network was constructed basing on the top 300 DEGs. The red icons represent up-regulated genes and the blue ones represent down-regulated genes. Furthermore, the connecting lines between the icons indicate potential interaction between different DEGs. (B) Module analysis of the DEGs enrolled in PPI network using MCODE method. The top five ranking clusters are shown according to MCODE score. (C) Functional enrichment analysis of genes in cluster 1. Likewise, the y axis and x axis represent enrichment terms and scores, respectively, and the color means p- value. (D) The top 10 hub genes are identified from PPI network using MCC method. The color represents MCC score. A darker red icon means higher MCC score and a lighter yellow one represents lower MCC score. (E) mRNA expression levels of CCL13, CCR2, FPR3 and PLAU in alveolar macrophages isolated from better prognosis subjects (VFDs > 12) and from poor prognosis individuals (VFDs <12).
    Figure Legend Snippet: (A) PPI network was constructed basing on the top 300 DEGs. The red icons represent up-regulated genes and the blue ones represent down-regulated genes. Furthermore, the connecting lines between the icons indicate potential interaction between different DEGs. (B) Module analysis of the DEGs enrolled in PPI network using MCODE method. The top five ranking clusters are shown according to MCODE score. (C) Functional enrichment analysis of genes in cluster 1. Likewise, the y axis and x axis represent enrichment terms and scores, respectively, and the color means p- value. (D) The top 10 hub genes are identified from PPI network using MCC method. The color represents MCC score. A darker red icon means higher MCC score and a lighter yellow one represents lower MCC score. (E) mRNA expression levels of CCL13, CCR2, FPR3 and PLAU in alveolar macrophages isolated from better prognosis subjects (VFDs > 12) and from poor prognosis individuals (VFDs <12).

    Techniques Used: Construct, Functional Assay, Expressing, Isolation

    (A) Relative mRNA expressions of CCL13, CCR2, CX3CR1, CXCL16, FPR3 and PLAU on THP-1-derived macrophages in response to LPS were assessed using qRT-PCR. (B) The protein levels of CCR2 and FPR3 under a varying time of LPS treatment were evaluated by Western blot analysis. (C) CCR2 expression on surface of THP-1-derived macrophages after LPS treatment was detected by flow cytometry analysis. (D) Relative mRNA expressions of CCR2 and FPR3 on primary AMs collected from patients and volunteers were evaluated using qRT-PCR. (E) The protein levels of CCR2 and FPR3 in primary AMs were examined using Western blot assay. (F) CCR2 expression on surface of primary AMs was detected by flow cytometry analysis. Data are presented as mean ± SD and are representative of three independent experiments. ∗ P < 0.05, by unpaired, 2-tailed Student’s t test.
    Figure Legend Snippet: (A) Relative mRNA expressions of CCL13, CCR2, CX3CR1, CXCL16, FPR3 and PLAU on THP-1-derived macrophages in response to LPS were assessed using qRT-PCR. (B) The protein levels of CCR2 and FPR3 under a varying time of LPS treatment were evaluated by Western blot analysis. (C) CCR2 expression on surface of THP-1-derived macrophages after LPS treatment was detected by flow cytometry analysis. (D) Relative mRNA expressions of CCR2 and FPR3 on primary AMs collected from patients and volunteers were evaluated using qRT-PCR. (E) The protein levels of CCR2 and FPR3 in primary AMs were examined using Western blot assay. (F) CCR2 expression on surface of primary AMs was detected by flow cytometry analysis. Data are presented as mean ± SD and are representative of three independent experiments. ∗ P < 0.05, by unpaired, 2-tailed Student’s t test.

    Techniques Used: Derivative Assay, Quantitative RT-PCR, Western Blot, Expressing, Flow Cytometry

    (A)Diagrammatic illustration for the chemotaxis assay procedure: Upper:1 ×10 4 of wild-type or siRNA-transfected macrophages were cultured in serum-free medium with or without LPS. Lower: Culture medium with or without CCL2/fMLP. (B) LPS-induced macrophage chemotaxis toward chemokine CCL2 was assessed using a transwell assay as described in the Methods. (C) Likewise, LPS-triggered macrophage migration toward fMLP was evaluated as above. (D) The correlation between CCR2 and FPR3 expression was analyzed using pearson correlation analysis with expression data of GSE89953 and GSE116560 . (E) Elevated protein expression of CCR2 induced by LPS stimulation was significantly attenuated by siRNA-FPR3 transfection. Data are presented as mean ± SD and are representative of 3 independent experiments. ∗ P < 0.05, by unpaired, two-tailed Student’s t test.
    Figure Legend Snippet: (A)Diagrammatic illustration for the chemotaxis assay procedure: Upper:1 ×10 4 of wild-type or siRNA-transfected macrophages were cultured in serum-free medium with or without LPS. Lower: Culture medium with or without CCL2/fMLP. (B) LPS-induced macrophage chemotaxis toward chemokine CCL2 was assessed using a transwell assay as described in the Methods. (C) Likewise, LPS-triggered macrophage migration toward fMLP was evaluated as above. (D) The correlation between CCR2 and FPR3 expression was analyzed using pearson correlation analysis with expression data of GSE89953 and GSE116560 . (E) Elevated protein expression of CCR2 induced by LPS stimulation was significantly attenuated by siRNA-FPR3 transfection. Data are presented as mean ± SD and are representative of 3 independent experiments. ∗ P < 0.05, by unpaired, two-tailed Student’s t test.

    Techniques Used: Chemotaxis Assay, Transfection, Cell Culture, Transwell Assay, Migration, Expressing, Two Tailed Test

    Related Articles

    Construct:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Functional Assay:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Expressing:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Isolation:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Derivative Assay:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Quantitative RT-PCR:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Western Blot:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Flow Cytometry:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Chemotaxis Assay:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Transfection:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Cell Culture:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Transwell Assay:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Migration:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Two Tailed Test:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    In Vitro:

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome.
    Article Snippet: Then, the membranes were incubated with 5% skim milk to block the non-specific sites.Then, the membranes were incubated with 5% skim milk to block the non-specific sites.. Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.. GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.GAPDH (1:5000, Proteintech, IL, USA) was simultaneously used as an internal control.



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    (A) PPI network was constructed basing on the top 300 DEGs. The red icons represent up-regulated genes and the blue ones represent down-regulated genes. Furthermore, the connecting lines between the icons indicate potential interaction between different DEGs. (B) Module analysis of the DEGs enrolled in PPI network using MCODE method. The top five ranking clusters are shown according to MCODE score. (C) Functional enrichment analysis of genes in cluster 1. Likewise, the y axis and x axis represent enrichment terms and scores, respectively, and the color means p- value. (D) The top 10 hub genes are identified from PPI network using MCC method. The color represents MCC score. A darker red icon means higher MCC score and a lighter yellow one represents lower MCC score. (E) mRNA expression levels of CCL13, CCR2, <t>FPR3</t> and PLAU in alveolar macrophages isolated from better prognosis subjects (VFDs > 12) and from poor prognosis individuals (VFDs <12).
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    Absolute Biotech Inc polyclonal rabbit anti-human fpr3 igg
    Cytokine production of allergen-treated DCs silenced for <t>FPR3</t> expression and cocultured CD4 + CD45RA + T cells. A, Supernatants of DCs silenced for FPR3 expression or controls activated with lipocalins, as indicated, were analyzed by means of ELISA for IL-12 p70. B-D, Supernatants of day 5 cocultures of DCs silenced for FPR3 expression and treated with Can f 1 or Fel d 4, as indicated, and naive CD4 + CD45RA + T cells were analyzed for IL-13 (Fig 4, B ), IL-4 (Fig 4, C ), and IFN-γ (Fig 4, D ) content. ns , P >.05, * P <.05, ** P <.01, and *** P <.001.
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    (A) PPI network was constructed basing on the top 300 DEGs. The red icons represent up-regulated genes and the blue ones represent down-regulated genes. Furthermore, the connecting lines between the icons indicate potential interaction between different DEGs. (B) Module analysis of the DEGs enrolled in PPI network using MCODE method. The top five ranking clusters are shown according to MCODE score. (C) Functional enrichment analysis of genes in cluster 1. Likewise, the y axis and x axis represent enrichment terms and scores, respectively, and the color means p- value. (D) The top 10 hub genes are identified from PPI network using MCC method. The color represents MCC score. A darker red icon means higher MCC score and a lighter yellow one represents lower MCC score. (E) mRNA expression levels of CCL13, CCR2, FPR3 and PLAU in alveolar macrophages isolated from better prognosis subjects (VFDs > 12) and from poor prognosis individuals (VFDs <12).

    Journal: PeerJ

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome

    doi: 10.7717/peerj.12312

    Figure Lengend Snippet: (A) PPI network was constructed basing on the top 300 DEGs. The red icons represent up-regulated genes and the blue ones represent down-regulated genes. Furthermore, the connecting lines between the icons indicate potential interaction between different DEGs. (B) Module analysis of the DEGs enrolled in PPI network using MCODE method. The top five ranking clusters are shown according to MCODE score. (C) Functional enrichment analysis of genes in cluster 1. Likewise, the y axis and x axis represent enrichment terms and scores, respectively, and the color means p- value. (D) The top 10 hub genes are identified from PPI network using MCC method. The color represents MCC score. A darker red icon means higher MCC score and a lighter yellow one represents lower MCC score. (E) mRNA expression levels of CCL13, CCR2, FPR3 and PLAU in alveolar macrophages isolated from better prognosis subjects (VFDs > 12) and from poor prognosis individuals (VFDs <12).

    Article Snippet: Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.

    Techniques: Construct, Functional Assay, Expressing, Isolation

    (A) Relative mRNA expressions of CCL13, CCR2, CX3CR1, CXCL16, FPR3 and PLAU on THP-1-derived macrophages in response to LPS were assessed using qRT-PCR. (B) The protein levels of CCR2 and FPR3 under a varying time of LPS treatment were evaluated by Western blot analysis. (C) CCR2 expression on surface of THP-1-derived macrophages after LPS treatment was detected by flow cytometry analysis. (D) Relative mRNA expressions of CCR2 and FPR3 on primary AMs collected from patients and volunteers were evaluated using qRT-PCR. (E) The protein levels of CCR2 and FPR3 in primary AMs were examined using Western blot assay. (F) CCR2 expression on surface of primary AMs was detected by flow cytometry analysis. Data are presented as mean ± SD and are representative of three independent experiments. ∗ P < 0.05, by unpaired, 2-tailed Student’s t test.

    Journal: PeerJ

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome

    doi: 10.7717/peerj.12312

    Figure Lengend Snippet: (A) Relative mRNA expressions of CCL13, CCR2, CX3CR1, CXCL16, FPR3 and PLAU on THP-1-derived macrophages in response to LPS were assessed using qRT-PCR. (B) The protein levels of CCR2 and FPR3 under a varying time of LPS treatment were evaluated by Western blot analysis. (C) CCR2 expression on surface of THP-1-derived macrophages after LPS treatment was detected by flow cytometry analysis. (D) Relative mRNA expressions of CCR2 and FPR3 on primary AMs collected from patients and volunteers were evaluated using qRT-PCR. (E) The protein levels of CCR2 and FPR3 in primary AMs were examined using Western blot assay. (F) CCR2 expression on surface of primary AMs was detected by flow cytometry analysis. Data are presented as mean ± SD and are representative of three independent experiments. ∗ P < 0.05, by unpaired, 2-tailed Student’s t test.

    Article Snippet: Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.

    Techniques: Derivative Assay, Quantitative RT-PCR, Western Blot, Expressing, Flow Cytometry

    (A)Diagrammatic illustration for the chemotaxis assay procedure: Upper:1 ×10 4 of wild-type or siRNA-transfected macrophages were cultured in serum-free medium with or without LPS. Lower: Culture medium with or without CCL2/fMLP. (B) LPS-induced macrophage chemotaxis toward chemokine CCL2 was assessed using a transwell assay as described in the Methods. (C) Likewise, LPS-triggered macrophage migration toward fMLP was evaluated as above. (D) The correlation between CCR2 and FPR3 expression was analyzed using pearson correlation analysis with expression data of GSE89953 and GSE116560 . (E) Elevated protein expression of CCR2 induced by LPS stimulation was significantly attenuated by siRNA-FPR3 transfection. Data are presented as mean ± SD and are representative of 3 independent experiments. ∗ P < 0.05, by unpaired, two-tailed Student’s t test.

    Journal: PeerJ

    Article Title: Identification and validation of candidate genes dysregulated in alveolar macrophages of acute respiratory distress syndrome

    doi: 10.7717/peerj.12312

    Figure Lengend Snippet: (A)Diagrammatic illustration for the chemotaxis assay procedure: Upper:1 ×10 4 of wild-type or siRNA-transfected macrophages were cultured in serum-free medium with or without LPS. Lower: Culture medium with or without CCL2/fMLP. (B) LPS-induced macrophage chemotaxis toward chemokine CCL2 was assessed using a transwell assay as described in the Methods. (C) Likewise, LPS-triggered macrophage migration toward fMLP was evaluated as above. (D) The correlation between CCR2 and FPR3 expression was analyzed using pearson correlation analysis with expression data of GSE89953 and GSE116560 . (E) Elevated protein expression of CCR2 induced by LPS stimulation was significantly attenuated by siRNA-FPR3 transfection. Data are presented as mean ± SD and are representative of 3 independent experiments. ∗ P < 0.05, by unpaired, two-tailed Student’s t test.

    Article Snippet: Rabbit polyclonal anti-human FPR3 antibody (orb608040, Biorbyt, UK), rabbit polyclonal anti-human CCR2 antibody (NBP1-48337, Novus Biologicals, USA) and HRP-conjugated secondary antibody (1:2000, Proteintech, IL, USA) were used.

    Techniques: Chemotaxis Assay, Transfection, Cell Culture, Transwell Assay, Migration, Expressing, Two Tailed Test

    Cytokine production of allergen-treated DCs silenced for FPR3 expression and cocultured CD4 + CD45RA + T cells. A, Supernatants of DCs silenced for FPR3 expression or controls activated with lipocalins, as indicated, were analyzed by means of ELISA for IL-12 p70. B-D, Supernatants of day 5 cocultures of DCs silenced for FPR3 expression and treated with Can f 1 or Fel d 4, as indicated, and naive CD4 + CD45RA + T cells were analyzed for IL-13 (Fig 4, B ), IL-4 (Fig 4, C ), and IFN-γ (Fig 4, D ) content. ns , P >.05, * P <.05, ** P <.01, and *** P <.001.

    Journal: The Journal of allergy and clinical immunology

    Article Title: Peptides from allergenic lipocalins bind to formyl peptide receptor 3 in human dendritic cells to mediate T H 2 immunity

    doi: 10.1016/j.jaci.2019.07.008

    Figure Lengend Snippet: Cytokine production of allergen-treated DCs silenced for FPR3 expression and cocultured CD4 + CD45RA + T cells. A, Supernatants of DCs silenced for FPR3 expression or controls activated with lipocalins, as indicated, were analyzed by means of ELISA for IL-12 p70. B-D, Supernatants of day 5 cocultures of DCs silenced for FPR3 expression and treated with Can f 1 or Fel d 4, as indicated, and naive CD4 + CD45RA + T cells were analyzed for IL-13 (Fig 4, B ), IL-4 (Fig 4, C ), and IFN-γ (Fig 4, D ) content. ns , P >.05, * P <.05, ** P <.01, and *** P <.001.

    Article Snippet: Immunostaining was performed with polyclonal rabbit anti-human FPR3 IgG (LSBio, Seattle, Wash), followed by Alexa Fluor 488–conjugated goat antirabbit antibody (Invitrogen Life Technologies, Eugene, Oreg).

    Techniques: Expressing, Enzyme-linked Immunosorbent Assay

    Effect of WRW4 on FPR3-induced T H 2 bias. A, WRW4 (1 μmol/L) was added before addition of Can f 1 digest and ionomycin to HEK 293–FPR3 cells. B, IL-12 production by DCs treated with allergenic and nonallergenic lipocalins in the presence or absence of 1 μmol/L WRW4, as indicated. C-E, IL-13 (Fig 5, C ), IL-4 (Fig 5, D ), and IFN-γ (Fig 5, E ) content in supernatants of cocultures of CD4 + CD45RA + naive T H cells and DCs treated with allergenic and nonallergenic lipocalins in the presence or absence of WRW4, as indicated. ns, P >.05, ** P <.01, and *** P <.001.

    Journal: The Journal of allergy and clinical immunology

    Article Title: Peptides from allergenic lipocalins bind to formyl peptide receptor 3 in human dendritic cells to mediate T H 2 immunity

    doi: 10.1016/j.jaci.2019.07.008

    Figure Lengend Snippet: Effect of WRW4 on FPR3-induced T H 2 bias. A, WRW4 (1 μmol/L) was added before addition of Can f 1 digest and ionomycin to HEK 293–FPR3 cells. B, IL-12 production by DCs treated with allergenic and nonallergenic lipocalins in the presence or absence of 1 μmol/L WRW4, as indicated. C-E, IL-13 (Fig 5, C ), IL-4 (Fig 5, D ), and IFN-γ (Fig 5, E ) content in supernatants of cocultures of CD4 + CD45RA + naive T H cells and DCs treated with allergenic and nonallergenic lipocalins in the presence or absence of WRW4, as indicated. ns, P >.05, ** P <.01, and *** P <.001.

    Article Snippet: Immunostaining was performed with polyclonal rabbit anti-human FPR3 IgG (LSBio, Seattle, Wash), followed by Alexa Fluor 488–conjugated goat antirabbit antibody (Invitrogen Life Technologies, Eugene, Oreg).

    Techniques: