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shctrl constructs  (OriGene)


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    Structured Review

    OriGene shctrl constructs
    Shctrl Constructs, supplied by OriGene, used in various techniques. Bioz Stars score: 96/100, based on 207 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/shctrl+constructs/Scrambled+shRNA+control+in+pGFP-C-shLenti+shRNA+Vector/pm38873940-270-3-8
    Average 96 stars, based on 207 article reviews
    shctrl constructs - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Expressing:

    Article Title: S1P-S1PR1 signaling impairs CD8 + T cell metabolism and effector function in tumors.
    Article Snippet: • In selected experiments, mice received anti-PD-1 antibody (200 μg/mouse) or isotype control IgG, administered three times per week. shRNA mediated knockdown of T cells • HEK 293 T (ATCC) cells were cultured in T75 tissue culture flasks (Falcon, NY, USA) under standard conditions (37 °C, 5% CO2). .. Cells were maintained in complete DMEM (Gibco, Thermo Fisher Scientific) supplemented with:10% fetal bovine serum (FBS; Gibco), 1% penicillin–streptomycin (Gibco) • For lentiviral production, HEK293T cells were co-transfected with: • 15 μg lentiviral expression plasmid encoding S1pr1 shRNA, Eif2ak3 shRNA, or non-targeting scrambled shRNA control (Origene, USA) • 10 μg psPAX2 packaging plasmid • 5 μg pMD2.G envelope plasmid • Transfection was carried out using the CaCl2/HBS precipitation method. ..

    Article Title: Multiple motor proteins regulate TDP-43 anterograde axonal transport.
    Article Snippet: .. Lentiviral vectors transduction for protein–protein interaction experiments Lentiviral (LV) constructs expressing short hairpin RNA (shRNA) targeting KLC1 with the fluorescent reporter TurboGFP (LV-shKLC1-tGFP), or a scrambled shRNA control with tGFP (LV-scramble-tGFP), were designed for expression under the human synapsin 1 (hSyn1) promoter, and were cloned and packaged by OriGene (Rockville, MD, US). ..

    Plasmid Preparation:

    Article Title: S1P-S1PR1 signaling impairs CD8 + T cell metabolism and effector function in tumors.
    Article Snippet: • In selected experiments, mice received anti-PD-1 antibody (200 μg/mouse) or isotype control IgG, administered three times per week. shRNA mediated knockdown of T cells • HEK 293 T (ATCC) cells were cultured in T75 tissue culture flasks (Falcon, NY, USA) under standard conditions (37 °C, 5% CO2). .. Cells were maintained in complete DMEM (Gibco, Thermo Fisher Scientific) supplemented with:10% fetal bovine serum (FBS; Gibco), 1% penicillin–streptomycin (Gibco) • For lentiviral production, HEK293T cells were co-transfected with: • 15 μg lentiviral expression plasmid encoding S1pr1 shRNA, Eif2ak3 shRNA, or non-targeting scrambled shRNA control (Origene, USA) • 10 μg psPAX2 packaging plasmid • 5 μg pMD2.G envelope plasmid • Transfection was carried out using the CaCl2/HBS precipitation method. ..

    shRNA:

    Article Title: S1P-S1PR1 signaling impairs CD8 + T cell metabolism and effector function in tumors.
    Article Snippet: • In selected experiments, mice received anti-PD-1 antibody (200 μg/mouse) or isotype control IgG, administered three times per week. shRNA mediated knockdown of T cells • HEK 293 T (ATCC) cells were cultured in T75 tissue culture flasks (Falcon, NY, USA) under standard conditions (37 °C, 5% CO2). .. Cells were maintained in complete DMEM (Gibco, Thermo Fisher Scientific) supplemented with:10% fetal bovine serum (FBS; Gibco), 1% penicillin–streptomycin (Gibco) • For lentiviral production, HEK293T cells were co-transfected with: • 15 μg lentiviral expression plasmid encoding S1pr1 shRNA, Eif2ak3 shRNA, or non-targeting scrambled shRNA control (Origene, USA) • 10 μg psPAX2 packaging plasmid • 5 μg pMD2.G envelope plasmid • Transfection was carried out using the CaCl2/HBS precipitation method. ..

    Article Title: Hippocalcin Regulates NMDA Receptor Function and Neuronal Activity Through Elavl3 in Mouse Hippocampal Neural Precursor Cells
    Article Snippet: Differentiation was induced by culturing NPCs in NB medium supplemented with 2% ( v / v ) B27 (Gibco) serum-free supplement, 0.5 mM L-glutamine, and 1% 100× penicillin-streptomycin antibiotic mixture for 5 days. .. For Gene silencing, the 4 unique 29-mer shRNA constructs designed to target mouse Hpca (Cat# TL515389), the 4 unique 29-mer shRNA constructs designed to target mouse Elavl3 (Cat# TL512545) and non-effective 29-mer scrambled negative control shRNA (Cat# TR30021) were purchased from OriGene Technologies Inc. (Rockville, MD, USA). .. Lentiviral particles were produced by co-transfection of control or Hpca shRNA with lentiviral packaging plasmids, pLP1, pLP2, and pLP/VSVG (Invitrogen) into HEK293T cells (ATCC, Manassas, VA, USA) using Lipofectamine 3000 (Invitrogen).

    Article Title: Development of antibody-drug conjugates targeting L1CAM to treat metastatic cancer
    Article Snippet: For knocking down L1CAM in PDXs, L1CAM human shRNA plasmid kit (Origene Cat# TL303597) was used. .. ShControl cells were generated in both cases by transducing the cells with scrambled shRNA control (Origene Cat# TR30021). ..

    Article Title: Glucose-stimulated KIF5B-driven microtubule sliding organizes microtubule networks in mouse pancreatic β cells
    Article Snippet: The Kif5b -targeting shRNA [shRNA Kif5b ] #1, [TL510740B, 5’- ACTCTACGGAACACTATTCAGTGGCTGGA ] and [shRNA Kif5b ] #2, [TL51074CB 5’ – AGACCGTAAACGCTATCAGCAAGAAGTAG ] are in the plasmid backbone pGFP-C-shLenti and were from Origene (Rockville, MD, USA). .. The nontargeting shRNA control was pGFP-C-shLenti, also from Origene. ..

    Article Title: Multiple motor proteins regulate TDP-43 anterograde axonal transport.
    Article Snippet: .. Lentiviral vectors transduction for protein–protein interaction experiments Lentiviral (LV) constructs expressing short hairpin RNA (shRNA) targeting KLC1 with the fluorescent reporter TurboGFP (LV-shKLC1-tGFP), or a scrambled shRNA control with tGFP (LV-scramble-tGFP), were designed for expression under the human synapsin 1 (hSyn1) promoter, and were cloned and packaged by OriGene (Rockville, MD, US). ..

    Article Title: CHD7 regulates cardiac neural crest cell differentiation through SOX5-mediated self-activation
    Article Snippet: SOX5-shRNA2 , Millipore Sigma , Cat#TRCN0000075497. .. scramble shRNA , Origene , CatTR30021V. ..

    Article Title: Sertad1 is elevated and plays a necessary role in neuron loss and cognitive impairment in a mouse model of Alzheimer's disease
    Article Snippet: .. The nontargeting scrambled shRNA-expressing GFP was purchased from Origene (catalog no.: TR30021V). .. 5xFAD (AD transgenic) mice and their nontransgenic WT littermates, C57BL6 mice were procured from The Jackson Laboratory.

    Control:

    Article Title: S1P-S1PR1 signaling impairs CD8 + T cell metabolism and effector function in tumors.
    Article Snippet: • In selected experiments, mice received anti-PD-1 antibody (200 μg/mouse) or isotype control IgG, administered three times per week. shRNA mediated knockdown of T cells • HEK 293 T (ATCC) cells were cultured in T75 tissue culture flasks (Falcon, NY, USA) under standard conditions (37 °C, 5% CO2). .. Cells were maintained in complete DMEM (Gibco, Thermo Fisher Scientific) supplemented with:10% fetal bovine serum (FBS; Gibco), 1% penicillin–streptomycin (Gibco) • For lentiviral production, HEK293T cells were co-transfected with: • 15 μg lentiviral expression plasmid encoding S1pr1 shRNA, Eif2ak3 shRNA, or non-targeting scrambled shRNA control (Origene, USA) • 10 μg psPAX2 packaging plasmid • 5 μg pMD2.G envelope plasmid • Transfection was carried out using the CaCl2/HBS precipitation method. ..

    Article Title: Development of antibody-drug conjugates targeting L1CAM to treat metastatic cancer
    Article Snippet: For knocking down L1CAM in PDXs, L1CAM human shRNA plasmid kit (Origene Cat# TL303597) was used. .. ShControl cells were generated in both cases by transducing the cells with scrambled shRNA control (Origene Cat# TR30021). ..

    Article Title: Glucose-stimulated KIF5B-driven microtubule sliding organizes microtubule networks in mouse pancreatic β cells
    Article Snippet: The Kif5b -targeting shRNA [shRNA Kif5b ] #1, [TL510740B, 5’- ACTCTACGGAACACTATTCAGTGGCTGGA ] and [shRNA Kif5b ] #2, [TL51074CB 5’ – AGACCGTAAACGCTATCAGCAAGAAGTAG ] are in the plasmid backbone pGFP-C-shLenti and were from Origene (Rockville, MD, USA). .. The nontargeting shRNA control was pGFP-C-shLenti, also from Origene. ..

    Article Title: Multiple motor proteins regulate TDP-43 anterograde axonal transport.
    Article Snippet: .. Lentiviral vectors transduction for protein–protein interaction experiments Lentiviral (LV) constructs expressing short hairpin RNA (shRNA) targeting KLC1 with the fluorescent reporter TurboGFP (LV-shKLC1-tGFP), or a scrambled shRNA control with tGFP (LV-scramble-tGFP), were designed for expression under the human synapsin 1 (hSyn1) promoter, and were cloned and packaged by OriGene (Rockville, MD, US). ..

    Transfection:

    Article Title: S1P-S1PR1 signaling impairs CD8 + T cell metabolism and effector function in tumors.
    Article Snippet: • In selected experiments, mice received anti-PD-1 antibody (200 μg/mouse) or isotype control IgG, administered three times per week. shRNA mediated knockdown of T cells • HEK 293 T (ATCC) cells were cultured in T75 tissue culture flasks (Falcon, NY, USA) under standard conditions (37 °C, 5% CO2). .. Cells were maintained in complete DMEM (Gibco, Thermo Fisher Scientific) supplemented with:10% fetal bovine serum (FBS; Gibco), 1% penicillin–streptomycin (Gibco) • For lentiviral production, HEK293T cells were co-transfected with: • 15 μg lentiviral expression plasmid encoding S1pr1 shRNA, Eif2ak3 shRNA, or non-targeting scrambled shRNA control (Origene, USA) • 10 μg psPAX2 packaging plasmid • 5 μg pMD2.G envelope plasmid • Transfection was carried out using the CaCl2/HBS precipitation method. ..

    Construct:

    Article Title: Hippocalcin Regulates NMDA Receptor Function and Neuronal Activity Through Elavl3 in Mouse Hippocampal Neural Precursor Cells
    Article Snippet: Differentiation was induced by culturing NPCs in NB medium supplemented with 2% ( v / v ) B27 (Gibco) serum-free supplement, 0.5 mM L-glutamine, and 1% 100× penicillin-streptomycin antibiotic mixture for 5 days. .. For Gene silencing, the 4 unique 29-mer shRNA constructs designed to target mouse Hpca (Cat# TL515389), the 4 unique 29-mer shRNA constructs designed to target mouse Elavl3 (Cat# TL512545) and non-effective 29-mer scrambled negative control shRNA (Cat# TR30021) were purchased from OriGene Technologies Inc. (Rockville, MD, USA). .. Lentiviral particles were produced by co-transfection of control or Hpca shRNA with lentiviral packaging plasmids, pLP1, pLP2, and pLP/VSVG (Invitrogen) into HEK293T cells (ATCC, Manassas, VA, USA) using Lipofectamine 3000 (Invitrogen).

    Article Title: Multiple motor proteins regulate TDP-43 anterograde axonal transport.
    Article Snippet: .. Lentiviral vectors transduction for protein–protein interaction experiments Lentiviral (LV) constructs expressing short hairpin RNA (shRNA) targeting KLC1 with the fluorescent reporter TurboGFP (LV-shKLC1-tGFP), or a scrambled shRNA control with tGFP (LV-scramble-tGFP), were designed for expression under the human synapsin 1 (hSyn1) promoter, and were cloned and packaged by OriGene (Rockville, MD, US). ..

    Negative Control:

    Article Title: Hippocalcin Regulates NMDA Receptor Function and Neuronal Activity Through Elavl3 in Mouse Hippocampal Neural Precursor Cells
    Article Snippet: Differentiation was induced by culturing NPCs in NB medium supplemented with 2% ( v / v ) B27 (Gibco) serum-free supplement, 0.5 mM L-glutamine, and 1% 100× penicillin-streptomycin antibiotic mixture for 5 days. .. For Gene silencing, the 4 unique 29-mer shRNA constructs designed to target mouse Hpca (Cat# TL515389), the 4 unique 29-mer shRNA constructs designed to target mouse Elavl3 (Cat# TL512545) and non-effective 29-mer scrambled negative control shRNA (Cat# TR30021) were purchased from OriGene Technologies Inc. (Rockville, MD, USA). .. Lentiviral particles were produced by co-transfection of control or Hpca shRNA with lentiviral packaging plasmids, pLP1, pLP2, and pLP/VSVG (Invitrogen) into HEK293T cells (ATCC, Manassas, VA, USA) using Lipofectamine 3000 (Invitrogen).

    Generated:

    Article Title: Development of antibody-drug conjugates targeting L1CAM to treat metastatic cancer
    Article Snippet: For knocking down L1CAM in PDXs, L1CAM human shRNA plasmid kit (Origene Cat# TL303597) was used. .. ShControl cells were generated in both cases by transducing the cells with scrambled shRNA control (Origene Cat# TR30021). ..

    Transduction:

    Article Title: Multiple motor proteins regulate TDP-43 anterograde axonal transport.
    Article Snippet: .. Lentiviral vectors transduction for protein–protein interaction experiments Lentiviral (LV) constructs expressing short hairpin RNA (shRNA) targeting KLC1 with the fluorescent reporter TurboGFP (LV-shKLC1-tGFP), or a scrambled shRNA control with tGFP (LV-scramble-tGFP), were designed for expression under the human synapsin 1 (hSyn1) promoter, and were cloned and packaged by OriGene (Rockville, MD, US). ..

    Clone Assay:

    Article Title: Multiple motor proteins regulate TDP-43 anterograde axonal transport.
    Article Snippet: .. Lentiviral vectors transduction for protein–protein interaction experiments Lentiviral (LV) constructs expressing short hairpin RNA (shRNA) targeting KLC1 with the fluorescent reporter TurboGFP (LV-shKLC1-tGFP), or a scrambled shRNA control with tGFP (LV-scramble-tGFP), were designed for expression under the human synapsin 1 (hSyn1) promoter, and were cloned and packaged by OriGene (Rockville, MD, US). ..



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    Silencing of integrin a6 in MES-GSCs does not have an impact on stemness and self-renewal. ( A , C ) Representative Western blot of the lentiviral-based <t>shRNA</t> silencing of ITGA6 in PN-GIC2 ( A ) and MES-GSCs ( C ). The values indicated within blots are relative to the densitometric analysis. Numbers indicate the normalized integrin a6 intensity ratio relative to the mean of <t>normalized</t> <t>shCTRL</t> samples. ( B ) Assessment of self-renewal capacity (mean ± SEM; n = 3; unpaired t -test) and sphere size (mean ± SEM; n = 3; Mann–Whitney test) in PN-GSCs silenced for ITGA6 . Micrographs from representative fields of gliomaspheres (scale bar = 100 µm). ( D ) Self-renewal capacity (mean ± SEM; n = 4; unpaired t -test) and sphere size (mean ± SEM; n = 4; Mann–Whitney test) in MES-GSCs silenced for ITGA6 . The number of independent experiments— n , the number of gliomaspheres scored for each condition—N. The values specified within the bar plot indicate the mean relative self-renewal capacity. ( E ) Transcript levels of ITGA6 and NES detected by means of qPCR in shITGA6 PN-GSCs and MES-GSCs (mean ± SEM; n = 3; unpaired t -test). ( F ) Relative transcript amount of ALDH1A3 , a specific MES stem cell marker, in shITGA6 MES-GSCs (mean ± SEM; n = 3; unpaired t -test). *** p < 0.001; **** p < 0.0001.
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    Silencing of integrin a6 in MES-GSCs does not have an impact on stemness and self-renewal. ( A , C ) Representative Western blot of the lentiviral-based <t>shRNA</t> silencing of ITGA6 in PN-GIC2 ( A ) and MES-GSCs ( C ). The values indicated within blots are relative to the densitometric analysis. Numbers indicate the normalized integrin a6 intensity ratio relative to the mean of <t>normalized</t> <t>shCTRL</t> samples. ( B ) Assessment of self-renewal capacity (mean ± SEM; n = 3; unpaired t -test) and sphere size (mean ± SEM; n = 3; Mann–Whitney test) in PN-GSCs silenced for ITGA6 . Micrographs from representative fields of gliomaspheres (scale bar = 100 µm). ( D ) Self-renewal capacity (mean ± SEM; n = 4; unpaired t -test) and sphere size (mean ± SEM; n = 4; Mann–Whitney test) in MES-GSCs silenced for ITGA6 . The number of independent experiments— n , the number of gliomaspheres scored for each condition—N. The values specified within the bar plot indicate the mean relative self-renewal capacity. ( E ) Transcript levels of ITGA6 and NES detected by means of qPCR in shITGA6 PN-GSCs and MES-GSCs (mean ± SEM; n = 3; unpaired t -test). ( F ) Relative transcript amount of ALDH1A3 , a specific MES stem cell marker, in shITGA6 MES-GSCs (mean ± SEM; n = 3; unpaired t -test). *** p < 0.001; **** p < 0.0001.
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    Image Search Results


    a , Experimental design of biotinylation assays in cortical neurons under basal, cLTP and post-cLTP conditions. b , A representative αFLAG immunofluorescence image of cortical neurons expressing FLAG-APEX2 fused to a nuclear export signal sequence from a lentiviral vector. c , Proteomic analysis of streptavidin pulldown and input samples from cortical neurons subject to biotin labelling under basal conditions. d , Pulldown to input ratios as a function of the predicted number of surface tyrosines per protein. e , Volcano plot with enrichment scores for the indicated selection of protein sets (bubble size indicates protein number in each protein set). f , Tyrosine surface exposure in ribosomal proteins with low and high accessibility scores as determined by their streptavidin pulldown / input ratios. g , Accessibility scores corresponding to ribosomal proteins as a function of the number of surface tyrosines hidden in the 80S ribosome under basal (blue) and cLTP (orange) conditions. h , Proteomic analysis of cortical neurons under basal and cLTP conditions. Ribosomal proteins are indicated (red dots).

    Journal: bioRxiv

    Article Title: Concerted remodelling of the postsynaptic spine and RNA granule by cLTP

    doi: 10.1101/2025.07.16.665171

    Figure Lengend Snippet: a , Experimental design of biotinylation assays in cortical neurons under basal, cLTP and post-cLTP conditions. b , A representative αFLAG immunofluorescence image of cortical neurons expressing FLAG-APEX2 fused to a nuclear export signal sequence from a lentiviral vector. c , Proteomic analysis of streptavidin pulldown and input samples from cortical neurons subject to biotin labelling under basal conditions. d , Pulldown to input ratios as a function of the predicted number of surface tyrosines per protein. e , Volcano plot with enrichment scores for the indicated selection of protein sets (bubble size indicates protein number in each protein set). f , Tyrosine surface exposure in ribosomal proteins with low and high accessibility scores as determined by their streptavidin pulldown / input ratios. g , Accessibility scores corresponding to ribosomal proteins as a function of the number of surface tyrosines hidden in the 80S ribosome under basal (blue) and cLTP (orange) conditions. h , Proteomic analysis of cortical neurons under basal and cLTP conditions. Ribosomal proteins are indicated (red dots).

    Article Snippet: Lentiviral constructs pLKO-RFP-shCtrl (Addgene, 69040) and pLKO-RFP-shDbn1 containing the shRNA sequence GCAGTCTATCTTTGGTGACCA (TRCN0000090077) against the Dbn1 gene were used in knockdown experiments. pFUW-FLAG-APEX2, pFUW-FLAG-APEX2-DBN1 and pFUW-FLAG-APEX2-IGF2BP1 were used to perform accessibility and proximity assays, and derived from pcDNA3 APEX2-NES (Addgene, 49386) and pFUW (Addgene, 14882).

    Techniques: Immunofluorescence, Expressing, Sequencing, Plasmid Preparation, Selection

    Silencing of integrin a6 in MES-GSCs does not have an impact on stemness and self-renewal. ( A , C ) Representative Western blot of the lentiviral-based shRNA silencing of ITGA6 in PN-GIC2 ( A ) and MES-GSCs ( C ). The values indicated within blots are relative to the densitometric analysis. Numbers indicate the normalized integrin a6 intensity ratio relative to the mean of normalized shCTRL samples. ( B ) Assessment of self-renewal capacity (mean ± SEM; n = 3; unpaired t -test) and sphere size (mean ± SEM; n = 3; Mann–Whitney test) in PN-GSCs silenced for ITGA6 . Micrographs from representative fields of gliomaspheres (scale bar = 100 µm). ( D ) Self-renewal capacity (mean ± SEM; n = 4; unpaired t -test) and sphere size (mean ± SEM; n = 4; Mann–Whitney test) in MES-GSCs silenced for ITGA6 . The number of independent experiments— n , the number of gliomaspheres scored for each condition—N. The values specified within the bar plot indicate the mean relative self-renewal capacity. ( E ) Transcript levels of ITGA6 and NES detected by means of qPCR in shITGA6 PN-GSCs and MES-GSCs (mean ± SEM; n = 3; unpaired t -test). ( F ) Relative transcript amount of ALDH1A3 , a specific MES stem cell marker, in shITGA6 MES-GSCs (mean ± SEM; n = 3; unpaired t -test). *** p < 0.001; **** p < 0.0001.

    Journal: Cancers

    Article Title: Dual Role of Integrin Alpha-6 in Glioblastoma: Supporting Stemness in Proneural Stem-Like Cells While Inducing Radioresistance in Mesenchymal Stem-Like Cells

    doi: 10.3390/cancers13123055

    Figure Lengend Snippet: Silencing of integrin a6 in MES-GSCs does not have an impact on stemness and self-renewal. ( A , C ) Representative Western blot of the lentiviral-based shRNA silencing of ITGA6 in PN-GIC2 ( A ) and MES-GSCs ( C ). The values indicated within blots are relative to the densitometric analysis. Numbers indicate the normalized integrin a6 intensity ratio relative to the mean of normalized shCTRL samples. ( B ) Assessment of self-renewal capacity (mean ± SEM; n = 3; unpaired t -test) and sphere size (mean ± SEM; n = 3; Mann–Whitney test) in PN-GSCs silenced for ITGA6 . Micrographs from representative fields of gliomaspheres (scale bar = 100 µm). ( D ) Self-renewal capacity (mean ± SEM; n = 4; unpaired t -test) and sphere size (mean ± SEM; n = 4; Mann–Whitney test) in MES-GSCs silenced for ITGA6 . The number of independent experiments— n , the number of gliomaspheres scored for each condition—N. The values specified within the bar plot indicate the mean relative self-renewal capacity. ( E ) Transcript levels of ITGA6 and NES detected by means of qPCR in shITGA6 PN-GSCs and MES-GSCs (mean ± SEM; n = 3; unpaired t -test). ( F ) Relative transcript amount of ALDH1A3 , a specific MES stem cell marker, in shITGA6 MES-GSCs (mean ± SEM; n = 3; unpaired t -test). *** p < 0.001; **** p < 0.0001.

    Article Snippet: Non-targeting shRNA construct (shCTRL; source clone ID: RHS4348) and shITGA6 plasmid mapping against ITGA6 exon 15 (target sequence: AGGATATTGCTTTAGAAAT; source clone ID: V3LHS_326014) were purchased from Thermo-Scientific.

    Techniques: Western Blot, shRNA, MANN-WHITNEY, Marker