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appropriate igg isotype control  (Bio-Techne corporation)


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    Structured Review

    Bio-Techne corporation appropriate igg isotype control
    Appropriate Igg Isotype Control, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 57 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/appropriate igg isotype control/product/Bio-Techne corporation
    Average 94 stars, based on 57 article reviews
    appropriate igg isotype control - by Bioz Stars, 2026-03
    94/100 stars

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    B16.SIY cells were stimulated during 24h under serum-reduced conditions with or without IL-17A (200ng) in the presence of an IL-17RC blocking <t>antibody</t> <t>(5ug/mL)</t> or an isotype control (IC). (A) Relative amounts of Csf1 mRNA determined by RT-qPCR. (B) Concentration of CXCL1 determined by ELISA. (C) Relative amounts of Pdl1 transcripts determined by RT-qPCR. Levels of Csf1 and Pdl1 transcripts were relativized to the levels ofIC-treated samples. Results are shown as the mean ± SD of 3 replicates for each condition. P-values were calculated by Two-tailed unpaired t-test. Ns: non-significant.
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    R&D Systems igg r d systems cat baf108 rrid ab 355828
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    Image Search Results


    Journal: Cell Reports Medicine

    Article Title: A glucocorticoid spike derails muscle repair to heterotopic ossification after spinal cord injury

    doi: 10.1016/j.xcrm.2024.101849

    Figure Lengend Snippet:

    Article Snippet: Biotinylated normal goat IgG control , R&D Systems , Cat# BAF108; RRID: AB_355828.

    Techniques: Control, Recombinant, Plasmid Preparation, Staining, cDNA Synthesis, Concentration Assay, Bicinchoninic Acid Protein Assay, RNA Sequencing, Saline, Gene Expression, Microarray, Software, Western Blot, Imaging, Cytometry, Tomography

    B16.SIY cells were stimulated during 24h under serum-reduced conditions with or without IL-17A (200ng) in the presence of an IL-17RC blocking antibody (5ug/mL) or an isotype control (IC). (A) Relative amounts of Csf1 mRNA determined by RT-qPCR. (B) Concentration of CXCL1 determined by ELISA. (C) Relative amounts of Pdl1 transcripts determined by RT-qPCR. Levels of Csf1 and Pdl1 transcripts were relativized to the levels ofIC-treated samples. Results are shown as the mean ± SD of 3 replicates for each condition. P-values were calculated by Two-tailed unpaired t-test. Ns: non-significant.

    Journal: bioRxiv

    Article Title: Interleukin-17 signaling influences CD8 + T cell immunity and tumor progression according to the IL-17 receptor subunit expression pattern in cancer cells

    doi: 10.1101/2022.12.16.520754

    Figure Lengend Snippet: B16.SIY cells were stimulated during 24h under serum-reduced conditions with or without IL-17A (200ng) in the presence of an IL-17RC blocking antibody (5ug/mL) or an isotype control (IC). (A) Relative amounts of Csf1 mRNA determined by RT-qPCR. (B) Concentration of CXCL1 determined by ELISA. (C) Relative amounts of Pdl1 transcripts determined by RT-qPCR. Levels of Csf1 and Pdl1 transcripts were relativized to the levels ofIC-treated samples. Results are shown as the mean ± SD of 3 replicates for each condition. P-values were calculated by Two-tailed unpaired t-test. Ns: non-significant.

    Article Snippet: Goat IgG (5ug/mL, cat: BAF108, R&D) was used as a control.

    Techniques: Blocking Assay, Quantitative RT-PCR, Concentration Assay, Enzyme-linked Immunosorbent Assay, Two Tailed Test