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dbp lentiviruses expressing the flag peptide (lv-flag-dbp and control lv-flag)  (Shanghai GenePharma)

 
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    Structured Review

    Shanghai GenePharma dbp lentiviruses expressing the flag peptide (lv-flag-dbp and control lv-flag)
    <t>DBP</t> regulated CCL2 expression via the target gene TRIM55. a siDBP inhibited TRIM55 mRNA expression, but not the expression of six other genes. b DBP bound to the TRIM55 promoter, as revealed by chromatin immunoprecipitation sequencing (ChIP)-PCR. c DBP bound to the TRIM55 promoter (-2984 bp), as revealed by the dual luciferase assay. d The TRIM55 promoter was divided into three subregions. e The dual luciferase assay indicated that DBP specifically bound to the -2116–2984-bp region. f, g: siTRIM55-1 and siTRIM55-2 significantly inhibited TNF-α and CCL2 expression at both the mRNA and protein levels in MCs. h The rescue assay showed that DBP-mediated CCL2 upregulation was blocked by si-TRIM55-1. si-TRIM55-1 and si-TRIM55-2, two siRNAs targeting TRIM55; Lv-Flag, <t>lentivirus</t> control; Lv-Flag-DBP: DBP-expressing lentivirus. *p < 0.05, **p < 0.01; n = 3. All assays were repeated at least three times
    Dbp Lentiviruses Expressing The Flag Peptide (Lv Flag Dbp And Control Lv Flag), supplied by Shanghai GenePharma, 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/flag+control/dbp+lentiviruses+expressing+the+flag+peptide++lv+flag+dbp+and+control+lv+flag+/pmc06804544-307-0-20
    Average 90 stars, based on 1 article reviews
    dbp lentiviruses expressing the flag peptide (lv-flag-dbp and control lv-flag) - by Bioz Stars, 2026-11
    90/100 stars

    Images

    1) Product Images from "The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis"

    Article Title: The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis

    Journal: Cellular and Molecular Immunology

    doi: 10.1038/s41423-018-0020-4

    DBP regulated CCL2 expression via the target gene TRIM55. a siDBP inhibited TRIM55 mRNA expression, but not the expression of six other genes. b DBP bound to the TRIM55 promoter, as revealed by chromatin immunoprecipitation sequencing (ChIP)-PCR. c DBP bound to the TRIM55 promoter (-2984 bp), as revealed by the dual luciferase assay. d The TRIM55 promoter was divided into three subregions. e The dual luciferase assay indicated that DBP specifically bound to the -2116–2984-bp region. f, g: siTRIM55-1 and siTRIM55-2 significantly inhibited TNF-α and CCL2 expression at both the mRNA and protein levels in MCs. h The rescue assay showed that DBP-mediated CCL2 upregulation was blocked by si-TRIM55-1. si-TRIM55-1 and si-TRIM55-2, two siRNAs targeting TRIM55; Lv-Flag, lentivirus control; Lv-Flag-DBP: DBP-expressing lentivirus. *p < 0.05, **p < 0.01; n = 3. All assays were repeated at least three times
    Figure Legend Snippet: DBP regulated CCL2 expression via the target gene TRIM55. a siDBP inhibited TRIM55 mRNA expression, but not the expression of six other genes. b DBP bound to the TRIM55 promoter, as revealed by chromatin immunoprecipitation sequencing (ChIP)-PCR. c DBP bound to the TRIM55 promoter (-2984 bp), as revealed by the dual luciferase assay. d The TRIM55 promoter was divided into three subregions. e The dual luciferase assay indicated that DBP specifically bound to the -2116–2984-bp region. f, g: siTRIM55-1 and siTRIM55-2 significantly inhibited TNF-α and CCL2 expression at both the mRNA and protein levels in MCs. h The rescue assay showed that DBP-mediated CCL2 upregulation was blocked by si-TRIM55-1. si-TRIM55-1 and si-TRIM55-2, two siRNAs targeting TRIM55; Lv-Flag, lentivirus control; Lv-Flag-DBP: DBP-expressing lentivirus. *p < 0.05, **p < 0.01; n = 3. All assays were repeated at least three times

    Techniques Used: Expressing, ChIP-sequencing, Luciferase, Rescue Assay, Control

    Related Articles

    Expressing:

    Article Title: The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis
    Article Snippet: Cells were crosslinked with 1% (v/v) formaldehyde for 10 min, and nuclear DNA was isolated using an EZ-CHIP-KIT (Millipore, Billerica, MA, USA) and sheared by sonication employing a cell disruptor (Sonics VCX150, Sonics and Materials Inc., Newtown, CT, USA).

    Control:

    Article Title: The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis
    Article Snippet: Cells were crosslinked with 1% (v/v) formaldehyde for 10 min, and nuclear DNA was isolated using an EZ-CHIP-KIT (Millipore, Billerica, MA, USA) and sheared by sonication employing a cell disruptor (Sonics VCX150, Sonics and Materials Inc., Newtown, CT, USA).

    ChIP-sequencing:

    Article Title: The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis
    Article Snippet: Cells were crosslinked with 1% (v/v) formaldehyde for 10 min, and nuclear DNA was isolated using an EZ-CHIP-KIT (Millipore, Billerica, MA, USA) and sheared by sonication employing a cell disruptor (Sonics VCX150, Sonics and Materials Inc., Newtown, CT, USA).

    Luciferase:

    Article Title: The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis
    Article Snippet: Cells were crosslinked with 1% (v/v) formaldehyde for 10 min, and nuclear DNA was isolated using an EZ-CHIP-KIT (Millipore, Billerica, MA, USA) and sheared by sonication employing a cell disruptor (Sonics VCX150, Sonics and Materials Inc., Newtown, CT, USA).

    Rescue Assay:

    Article Title: The role of transcriptional factor D-site-binding protein in circadian CCL2 gene expression in anti-Thy1 nephritis
    Article Snippet: Cells were crosslinked with 1% (v/v) formaldehyde for 10 min, and nuclear DNA was isolated using an EZ-CHIP-KIT (Millipore, Billerica, MA, USA) and sheared by sonication employing a cell disruptor (Sonics VCX150, Sonics and Materials Inc., Newtown, CT, USA).



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