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sirna negative control  (MedChemExpress)


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    Structured Review

    MedChemExpress sirna negative control
    Sirna Negative Control, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 52 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/sirna+negative+control/SiRNA+Negative+Control/custom%40hy-150150%4042217127
    Average 95 stars, based on 52 article reviews
    sirna negative control - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Negative Control:

    Article Title: Targeting NLRP1-CCL8 axis in the leukaemic niche suppresses AML via inhibition of PI3K-AKT signalling.
    Article Snippet: © 2025 British Society for Haematology and John Wiley & Sons Ltd. Xingyue Li, Qi Zhou and Xiaowen Hao contributed equally to this work.. 1Department of Hematology, Affiliated Hospital of Xuzhou Medical University, Xuzhou, China 2Key Laboratory of Bone Marrow Stem Cells, Xuzhou, Jiangsu Province, China 3Blood Diseases Institute, Xuzhou Medical University, Xuzhou, China 4Xuzhou Ruihu Health Management Consulting Co., Ltd, Xuzhou, China 5School of Medical Technology, Xuzhou Medical University, Xuzhou, China

    Transfection:

    Article Title: M1 macrophage-derived CXCL12 drives neurogenic heterotopic ossification following spinal cord injury
    Article Snippet: Data acquisition and analysis were performed with Accuri CFlow Plus software (version 1.0.227.4; BD Biosciences ). .. M1 macrophages were transfected with small interfering RNA (siRNA) and siRNA-negative control (NC) targeting CXCL12 (RiboBio, Guangzhou, China, Cat# siB1706200429) (Table 1), PI3K inhibitor (LY294002; Selleck, Houston, TX, USA, Cat# S1105, 10 μM), or CXCR4 inhibitor (AMD3100; MedChemExpress, Monmouth Junction, NJ, USA, Cat# HY-10046, 10 μM). siRNA and siRNA-NC were transfected using Lipofectamine 2000 (Invitrogen, Cat# 11668019). .. Mouse BMSCs (Zishan Biotech, Wuhan, China, Cat#STCC6011P ) were cultured in osteoblastic differentiation induction medium (Procell, Wuhan, China, Cat# CM-M121) with 5% CO2 at 37°C to induce osteogenesis.

    Small Interfering RNA:

    Article Title: M1 macrophage-derived CXCL12 drives neurogenic heterotopic ossification following spinal cord injury
    Article Snippet: Data acquisition and analysis were performed with Accuri CFlow Plus software (version 1.0.227.4; BD Biosciences ). .. M1 macrophages were transfected with small interfering RNA (siRNA) and siRNA-negative control (NC) targeting CXCL12 (RiboBio, Guangzhou, China, Cat# siB1706200429) (Table 1), PI3K inhibitor (LY294002; Selleck, Houston, TX, USA, Cat# S1105, 10 μM), or CXCR4 inhibitor (AMD3100; MedChemExpress, Monmouth Junction, NJ, USA, Cat# HY-10046, 10 μM). siRNA and siRNA-NC were transfected using Lipofectamine 2000 (Invitrogen, Cat# 11668019). .. Mouse BMSCs (Zishan Biotech, Wuhan, China, Cat#STCC6011P ) were cultured in osteoblastic differentiation induction medium (Procell, Wuhan, China, Cat# CM-M121) with 5% CO2 at 37°C to induce osteogenesis.

    Control:

    Article Title: M1 macrophage-derived CXCL12 drives neurogenic heterotopic ossification following spinal cord injury
    Article Snippet: Data acquisition and analysis were performed with Accuri CFlow Plus software (version 1.0.227.4; BD Biosciences ). .. M1 macrophages were transfected with small interfering RNA (siRNA) and siRNA-negative control (NC) targeting CXCL12 (RiboBio, Guangzhou, China, Cat# siB1706200429) (Table 1), PI3K inhibitor (LY294002; Selleck, Houston, TX, USA, Cat# S1105, 10 μM), or CXCR4 inhibitor (AMD3100; MedChemExpress, Monmouth Junction, NJ, USA, Cat# HY-10046, 10 μM). siRNA and siRNA-NC were transfected using Lipofectamine 2000 (Invitrogen, Cat# 11668019). .. Mouse BMSCs (Zishan Biotech, Wuhan, China, Cat#STCC6011P ) were cultured in osteoblastic differentiation induction medium (Procell, Wuhan, China, Cat# CM-M121) with 5% CO2 at 37°C to induce osteogenesis.



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    OriGene negative control sirna
    ( A, B ) G3BP1 was transiently silenced with <t>siRNA,</t> or not; cells were then serum-starved and stimulated with PDGF-BB, as indicated. Activation of PDGFR, STAT1, ERK1/2, AKT, PLCγ, and STAT3 signaling pathways was determined by immunoblotting for phosphorylated and total amounts of the signaling proteins. The experiments were repeated four times.
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    Image Search Results


    ( A, B ) G3BP1 was transiently silenced with siRNA, or not; cells were then serum-starved and stimulated with PDGF-BB, as indicated. Activation of PDGFR, STAT1, ERK1/2, AKT, PLCγ, and STAT3 signaling pathways was determined by immunoblotting for phosphorylated and total amounts of the signaling proteins. The experiments were repeated four times.

    Journal: Bioscience Reports

    Article Title: G3BP1 is a SWI/SNF-bound regulator of transcription that modulates activation of STATs

    doi: 10.1042/BSR20250290

    Figure Lengend Snippet: ( A, B ) G3BP1 was transiently silenced with siRNA, or not; cells were then serum-starved and stimulated with PDGF-BB, as indicated. Activation of PDGFR, STAT1, ERK1/2, AKT, PLCγ, and STAT3 signaling pathways was determined by immunoblotting for phosphorylated and total amounts of the signaling proteins. The experiments were repeated four times.

    Article Snippet: AG01523 cells were transiently transfected with 20 nM siRNA of Trilencer-27 G3BP siRNA (#SR, OriGene Technologies, U.S.A.) or 20 nM scrambled negative control siRNA (#SR30004, OriGene Technologies, U.S.A.), using SilentFect reagent (Bio-Rad), and incubated for 72 to 96 h at 37°C in a CO 2 incubator.

    Techniques: Activation Assay, Protein-Protein interactions, Western Blot

    (A–F) After transient silencing of G3BP1 with siRNA, or not, and serum starvation overnight, AG01523 cells were stimulated with PDGF-BB for 1 h (black bars) or left unstimulated (0 h, gray bars). mRNA expression of G3BP1 ( A ), STAT3 ( B ), STAT1 ( C ), FOS ( D ), MYC ( E ), and CCND1 (cyclin D1) ( F ) is presented relative to the expression of control gene HPRT . Statistical analysis was performed on four independent repeats using Student’s t -test. *, P- value <0.05; **, P <0.01. The experiments were repeated six times.

    Journal: Bioscience Reports

    Article Title: G3BP1 is a SWI/SNF-bound regulator of transcription that modulates activation of STATs

    doi: 10.1042/BSR20250290

    Figure Lengend Snippet: (A–F) After transient silencing of G3BP1 with siRNA, or not, and serum starvation overnight, AG01523 cells were stimulated with PDGF-BB for 1 h (black bars) or left unstimulated (0 h, gray bars). mRNA expression of G3BP1 ( A ), STAT3 ( B ), STAT1 ( C ), FOS ( D ), MYC ( E ), and CCND1 (cyclin D1) ( F ) is presented relative to the expression of control gene HPRT . Statistical analysis was performed on four independent repeats using Student’s t -test. *, P- value <0.05; **, P <0.01. The experiments were repeated six times.

    Article Snippet: AG01523 cells were transiently transfected with 20 nM siRNA of Trilencer-27 G3BP siRNA (#SR, OriGene Technologies, U.S.A.) or 20 nM scrambled negative control siRNA (#SR30004, OriGene Technologies, U.S.A.), using SilentFect reagent (Bio-Rad), and incubated for 72 to 96 h at 37°C in a CO 2 incubator.

    Techniques: Expressing, Control

    ( A ) G3BP1 was knocked down by siRNA, or not, in AG01523 fibroblasts. Cells were then grown in medium containing 1% FBS and increasing concentrations of PDGF-BB. The amount of DNA and, therefore, the proliferation rate was determined by measuring absorption of fluorescently labeled DNA-intercalating dye using the CyQuant assay. The experiments were repeated three times. ( B ) Schematic illustration of the findings of the study. G3BP1 acts as a co-activator of PDGF-BB-induced activation of STAT3 and as a co-repressor of the transcription of cyclin D1 and STAT1 due to its association with the SWI/SNF chromatin remodeling complex.

    Journal: Bioscience Reports

    Article Title: G3BP1 is a SWI/SNF-bound regulator of transcription that modulates activation of STATs

    doi: 10.1042/BSR20250290

    Figure Lengend Snippet: ( A ) G3BP1 was knocked down by siRNA, or not, in AG01523 fibroblasts. Cells were then grown in medium containing 1% FBS and increasing concentrations of PDGF-BB. The amount of DNA and, therefore, the proliferation rate was determined by measuring absorption of fluorescently labeled DNA-intercalating dye using the CyQuant assay. The experiments were repeated three times. ( B ) Schematic illustration of the findings of the study. G3BP1 acts as a co-activator of PDGF-BB-induced activation of STAT3 and as a co-repressor of the transcription of cyclin D1 and STAT1 due to its association with the SWI/SNF chromatin remodeling complex.

    Article Snippet: AG01523 cells were transiently transfected with 20 nM siRNA of Trilencer-27 G3BP siRNA (#SR, OriGene Technologies, U.S.A.) or 20 nM scrambled negative control siRNA (#SR30004, OriGene Technologies, U.S.A.), using SilentFect reagent (Bio-Rad), and incubated for 72 to 96 h at 37°C in a CO 2 incubator.

    Techniques: Labeling, CyQUANT Assay, Activation Assay