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control empty pfn2k vector  (OriGene)


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    Structured Review

    OriGene control empty pfn2k vector
    Control Empty Pfn2k Vector, supplied by OriGene, used in various techniques. Bioz Stars score: 91/100, based on 36 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/control+vectors/Negative+shRNA+control+in+pGFP-V-RS+Vector/pmc02709342-239-22-25
    Average 91 stars, based on 36 article reviews
    control empty pfn2k vector - by Bioz Stars, 2026-10
    91/100 stars

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    Related Articles

    Knockdown:

    Article Title: Altered glucuronidation deregulates androgen dependent response profiles and signifies castration resistance in prostate cancer
    Article Snippet: To generate UGDH overexpression lines, LNCaP AD and LNCaP CR cells were transduced with lentiviral particles packaged to contain plasmids encoding wild type UGDH with a C-terminal Flag epitope tag, or a vector control expressing EGFP (UGDH EX-Q0483-Lv102 and EX-EGFP-Lv105, respectively, from GeneCopoeia, Rockville, MD, USA). .. To achieve UGDH knockdown, LNCaP AD and LNCaP CR cells were transfected with plasmids encoding shRNA targeted to UGDH or a scrambled non-targeting control (UGDH shRNA-pGFP-V-RS #TG334012 and 29-mer oligo-pGFP-V-RS #TR30008, respectively, from Origene Technologies, Rockville, MD, USA). .. Stable integration of the overexpression, shRNA, and respective vector control plasmids was achieved by clonal selection in RPMI-1640 with 10% FBS and 1 μg/ml puromycin.

    Article Title: Endocannabinoid signalling in stem cells and cerebral organoids drives differentiation to deep layer projection neurons via CB 1 receptors.
    Article Snippet: .. CB1 receptor knockdown was performed in R1 mES cells with 10 μg pGFP-V-RS (Origene, Rockville, MD, USA) encoding shControl or D ev el o pm en t • A cc ep te d m an us cr ip t shCB1 nucleofection using Amaxa Nucleofector (AAB-1001, Lonza, program A013, 5x106 cells). .. Positive colonies were selected by puromycin (Sigma-Aldrich) and dissociated cells were cultured as described above.

    Transfection:

    Article Title: Altered glucuronidation deregulates androgen dependent response profiles and signifies castration resistance in prostate cancer
    Article Snippet: To generate UGDH overexpression lines, LNCaP AD and LNCaP CR cells were transduced with lentiviral particles packaged to contain plasmids encoding wild type UGDH with a C-terminal Flag epitope tag, or a vector control expressing EGFP (UGDH EX-Q0483-Lv102 and EX-EGFP-Lv105, respectively, from GeneCopoeia, Rockville, MD, USA). .. To achieve UGDH knockdown, LNCaP AD and LNCaP CR cells were transfected with plasmids encoding shRNA targeted to UGDH or a scrambled non-targeting control (UGDH shRNA-pGFP-V-RS #TG334012 and 29-mer oligo-pGFP-V-RS #TR30008, respectively, from Origene Technologies, Rockville, MD, USA). .. Stable integration of the overexpression, shRNA, and respective vector control plasmids was achieved by clonal selection in RPMI-1640 with 10% FBS and 1 μg/ml puromycin.

    Article Title: Pseudolaric Acid B Targets CD147 to Selectively Kill Acute Myeloid Leukemia Cells
    Article Snippet: .. CD147 gene-specific short hairpin RNA (shRNA-CD147-A and shRNA-CD147-B; OriGene; Rockville, MD, USA; see for sequences) and a scrambled shRNA negative control (shRNA-NC; OriGene) were transfected into HEK293T cells (cultured in antibiotic-free DMEM media with 10% FBS). .. Transfection was carried out with a TransIT-LT1 transfection reagent (MirusBio; Madison, WI, USA), according to the manufacturer’s protocol.

    Article Title: FAT4 loss initiates hepatocarcinogenesis through the switching of canonical to noncanonical WNT signaling pathways
    Article Snippet: .. Stable shRNA-mediated PAK6 transfection For stable clone generation, L02 cells with FAT4-KO were transfected with 2 μg of p21 (RAC1)-activated kinase 6 (PAK6)–specific shRNA or negative control shRNA (Origene) using LipofectamineTM 3000. ..

    Article Title: The Role of CPNE7 (Copine-7) in Colorectal Cancer Prognosis and Metastasis
    Article Snippet: For transfections, cells were incubated with CPNE7 shRNA (ORIGENE, Rockville, MD, USA, TL305242) at 50 μmol/L concentrations in Opti MEM medium. .. The transfection efficiencies of cell lines were tested by transfection of the shRNA plasmid negative control vector (ORIGENE, Rockville, MD, USA, TR30008). ..

    Article Title: Glia Maturation Factor-Gamma Regulates Autophagy and Scavenger Receptor-Mediated Phagocytosis in Murine Macrophages
    Article Snippet: For GMFγ + Nrf2 double-knockdown, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with an siRNA against Nrf2 (SR427248; ORIGENE), followed by transfection with an siRNA against GMFg for another 48 h, using Nucleofector II. .. For GMFγ overexpression studies, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with a GMFgGFP (ORIGENE) or GFP control plasmid (ORIGENE) using Nucleofector II. ..

    shRNA:

    Article Title: Altered glucuronidation deregulates androgen dependent response profiles and signifies castration resistance in prostate cancer
    Article Snippet: To generate UGDH overexpression lines, LNCaP AD and LNCaP CR cells were transduced with lentiviral particles packaged to contain plasmids encoding wild type UGDH with a C-terminal Flag epitope tag, or a vector control expressing EGFP (UGDH EX-Q0483-Lv102 and EX-EGFP-Lv105, respectively, from GeneCopoeia, Rockville, MD, USA). .. To achieve UGDH knockdown, LNCaP AD and LNCaP CR cells were transfected with plasmids encoding shRNA targeted to UGDH or a scrambled non-targeting control (UGDH shRNA-pGFP-V-RS #TG334012 and 29-mer oligo-pGFP-V-RS #TR30008, respectively, from Origene Technologies, Rockville, MD, USA). .. Stable integration of the overexpression, shRNA, and respective vector control plasmids was achieved by clonal selection in RPMI-1640 with 10% FBS and 1 μg/ml puromycin.

    Article Title: Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
    Article Snippet: Ba/F3 cells were plated onto 3.5 cm dishes coated with fibronectin fragments (Retronectin dish, Takara, Shiga, Japan) and cultured with 1 ml virus supernatant for 72 h. Retrovirus-infected Ba/F3 cells were isolated as GFP-positive cells by FACS Aria (BD Biosciences, Franklin Lakes, NJ). .. Expression vectors for CALM-specific shRNA and SCR shRNA (a negative control) were generated by cloning these sequences into pGFP-V-RS (OriGene Technologies, Rockville, MD). ..

    Article Title: Pseudolaric Acid B Targets CD147 to Selectively Kill Acute Myeloid Leukemia Cells
    Article Snippet: .. CD147 gene-specific short hairpin RNA (shRNA-CD147-A and shRNA-CD147-B; OriGene; Rockville, MD, USA; see for sequences) and a scrambled shRNA negative control (shRNA-NC; OriGene) were transfected into HEK293T cells (cultured in antibiotic-free DMEM media with 10% FBS). .. Transfection was carried out with a TransIT-LT1 transfection reagent (MirusBio; Madison, WI, USA), according to the manufacturer’s protocol.

    Article Title: FAT4 loss initiates hepatocarcinogenesis through the switching of canonical to noncanonical WNT signaling pathways
    Article Snippet: .. Stable shRNA-mediated PAK6 transfection For stable clone generation, L02 cells with FAT4-KO were transfected with 2 μg of p21 (RAC1)-activated kinase 6 (PAK6)–specific shRNA or negative control shRNA (Origene) using LipofectamineTM 3000. ..

    Article Title: The Role of CPNE7 (Copine-7) in Colorectal Cancer Prognosis and Metastasis
    Article Snippet: For transfections, cells were incubated with CPNE7 shRNA (ORIGENE, Rockville, MD, USA, TL305242) at 50 μmol/L concentrations in Opti MEM medium. .. The transfection efficiencies of cell lines were tested by transfection of the shRNA plasmid negative control vector (ORIGENE, Rockville, MD, USA, TR30008). ..

    Control:

    Article Title: Altered glucuronidation deregulates androgen dependent response profiles and signifies castration resistance in prostate cancer
    Article Snippet: To generate UGDH overexpression lines, LNCaP AD and LNCaP CR cells were transduced with lentiviral particles packaged to contain plasmids encoding wild type UGDH with a C-terminal Flag epitope tag, or a vector control expressing EGFP (UGDH EX-Q0483-Lv102 and EX-EGFP-Lv105, respectively, from GeneCopoeia, Rockville, MD, USA). .. To achieve UGDH knockdown, LNCaP AD and LNCaP CR cells were transfected with plasmids encoding shRNA targeted to UGDH or a scrambled non-targeting control (UGDH shRNA-pGFP-V-RS #TG334012 and 29-mer oligo-pGFP-V-RS #TR30008, respectively, from Origene Technologies, Rockville, MD, USA). .. Stable integration of the overexpression, shRNA, and respective vector control plasmids was achieved by clonal selection in RPMI-1640 with 10% FBS and 1 μg/ml puromycin.

    Article Title: Long non-coding RNA H19 promotes the proliferation, migration and invasion while inhibits apoptosis of hypertrophic scarring fibroblasts by targeting miR-3187-3p/GAB1 axis.
    Article Snippet: Background: It had been reported that long non-coding RNA (lncRNA) H19 was associated with the proliferation of fibroblasts.. However, the regulatory mechanism of H19 remains unclear.. Thus, the study was designed to explore the underlying mechanism of H19 in the process of Hypertrophic scarring (HS).

    Article Title: Glia Maturation Factor-Gamma Regulates Autophagy and Scavenger Receptor-Mediated Phagocytosis in Murine Macrophages
    Article Snippet: For GMFγ + Nrf2 double-knockdown, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with an siRNA against Nrf2 (SR427248; ORIGENE), followed by transfection with an siRNA against GMFg for another 48 h, using Nucleofector II. .. For GMFγ overexpression studies, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with a GMFgGFP (ORIGENE) or GFP control plasmid (ORIGENE) using Nucleofector II. ..

    Expressing:

    Article Title: Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
    Article Snippet: Ba/F3 cells were plated onto 3.5 cm dishes coated with fibronectin fragments (Retronectin dish, Takara, Shiga, Japan) and cultured with 1 ml virus supernatant for 72 h. Retrovirus-infected Ba/F3 cells were isolated as GFP-positive cells by FACS Aria (BD Biosciences, Franklin Lakes, NJ). .. Expression vectors for CALM-specific shRNA and SCR shRNA (a negative control) were generated by cloning these sequences into pGFP-V-RS (OriGene Technologies, Rockville, MD). ..

    Negative Control:

    Article Title: Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
    Article Snippet: Ba/F3 cells were plated onto 3.5 cm dishes coated with fibronectin fragments (Retronectin dish, Takara, Shiga, Japan) and cultured with 1 ml virus supernatant for 72 h. Retrovirus-infected Ba/F3 cells were isolated as GFP-positive cells by FACS Aria (BD Biosciences, Franklin Lakes, NJ). .. Expression vectors for CALM-specific shRNA and SCR shRNA (a negative control) were generated by cloning these sequences into pGFP-V-RS (OriGene Technologies, Rockville, MD). ..

    Article Title: Pseudolaric Acid B Targets CD147 to Selectively Kill Acute Myeloid Leukemia Cells
    Article Snippet: .. CD147 gene-specific short hairpin RNA (shRNA-CD147-A and shRNA-CD147-B; OriGene; Rockville, MD, USA; see for sequences) and a scrambled shRNA negative control (shRNA-NC; OriGene) were transfected into HEK293T cells (cultured in antibiotic-free DMEM media with 10% FBS). .. Transfection was carried out with a TransIT-LT1 transfection reagent (MirusBio; Madison, WI, USA), according to the manufacturer’s protocol.

    Article Title: Long non-coding RNA H19 promotes the proliferation, migration and invasion while inhibits apoptosis of hypertrophic scarring fibroblasts by targeting miR-3187-3p/GAB1 axis.
    Article Snippet: Background: It had been reported that long non-coding RNA (lncRNA) H19 was associated with the proliferation of fibroblasts.. However, the regulatory mechanism of H19 remains unclear.. Thus, the study was designed to explore the underlying mechanism of H19 in the process of Hypertrophic scarring (HS).

    Article Title: FAT4 loss initiates hepatocarcinogenesis through the switching of canonical to noncanonical WNT signaling pathways
    Article Snippet: .. Stable shRNA-mediated PAK6 transfection For stable clone generation, L02 cells with FAT4-KO were transfected with 2 μg of p21 (RAC1)-activated kinase 6 (PAK6)–specific shRNA or negative control shRNA (Origene) using LipofectamineTM 3000. ..

    Article Title: The Role of CPNE7 (Copine-7) in Colorectal Cancer Prognosis and Metastasis
    Article Snippet: For transfections, cells were incubated with CPNE7 shRNA (ORIGENE, Rockville, MD, USA, TL305242) at 50 μmol/L concentrations in Opti MEM medium. .. The transfection efficiencies of cell lines were tested by transfection of the shRNA plasmid negative control vector (ORIGENE, Rockville, MD, USA, TR30008). ..

    Generated:

    Article Title: Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
    Article Snippet: Ba/F3 cells were plated onto 3.5 cm dishes coated with fibronectin fragments (Retronectin dish, Takara, Shiga, Japan) and cultured with 1 ml virus supernatant for 72 h. Retrovirus-infected Ba/F3 cells were isolated as GFP-positive cells by FACS Aria (BD Biosciences, Franklin Lakes, NJ). .. Expression vectors for CALM-specific shRNA and SCR shRNA (a negative control) were generated by cloning these sequences into pGFP-V-RS (OriGene Technologies, Rockville, MD). ..

    Cloning:

    Article Title: Chlorpromazine eliminates acute myeloid leukemia cells by perturbing subcellular localization of FLT3-ITD and KIT-D816V
    Article Snippet: Ba/F3 cells were plated onto 3.5 cm dishes coated with fibronectin fragments (Retronectin dish, Takara, Shiga, Japan) and cultured with 1 ml virus supernatant for 72 h. Retrovirus-infected Ba/F3 cells were isolated as GFP-positive cells by FACS Aria (BD Biosciences, Franklin Lakes, NJ). .. Expression vectors for CALM-specific shRNA and SCR shRNA (a negative control) were generated by cloning these sequences into pGFP-V-RS (OriGene Technologies, Rockville, MD). ..

    Cell Culture:

    Article Title: Pseudolaric Acid B Targets CD147 to Selectively Kill Acute Myeloid Leukemia Cells
    Article Snippet: .. CD147 gene-specific short hairpin RNA (shRNA-CD147-A and shRNA-CD147-B; OriGene; Rockville, MD, USA; see for sequences) and a scrambled shRNA negative control (shRNA-NC; OriGene) were transfected into HEK293T cells (cultured in antibiotic-free DMEM media with 10% FBS). .. Transfection was carried out with a TransIT-LT1 transfection reagent (MirusBio; Madison, WI, USA), according to the manufacturer’s protocol.

    Small Interfering RNA:

    Article Title: Long non-coding RNA H19 promotes the proliferation, migration and invasion while inhibits apoptosis of hypertrophic scarring fibroblasts by targeting miR-3187-3p/GAB1 axis.
    Article Snippet: Background: It had been reported that long non-coding RNA (lncRNA) H19 was associated with the proliferation of fibroblasts.. However, the regulatory mechanism of H19 remains unclear.. Thus, the study was designed to explore the underlying mechanism of H19 in the process of Hypertrophic scarring (HS).

    Stable Transfection:

    Article Title: FAT4 loss initiates hepatocarcinogenesis through the switching of canonical to noncanonical WNT signaling pathways
    Article Snippet: .. Stable shRNA-mediated PAK6 transfection For stable clone generation, L02 cells with FAT4-KO were transfected with 2 μg of p21 (RAC1)-activated kinase 6 (PAK6)–specific shRNA or negative control shRNA (Origene) using LipofectamineTM 3000. ..

    Plasmid Preparation:

    Article Title: The Role of CPNE7 (Copine-7) in Colorectal Cancer Prognosis and Metastasis
    Article Snippet: For transfections, cells were incubated with CPNE7 shRNA (ORIGENE, Rockville, MD, USA, TL305242) at 50 μmol/L concentrations in Opti MEM medium. .. The transfection efficiencies of cell lines were tested by transfection of the shRNA plasmid negative control vector (ORIGENE, Rockville, MD, USA, TR30008). ..

    Article Title: Glia Maturation Factor-Gamma Regulates Autophagy and Scavenger Receptor-Mediated Phagocytosis in Murine Macrophages
    Article Snippet: For GMFγ + Nrf2 double-knockdown, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with an siRNA against Nrf2 (SR427248; ORIGENE), followed by transfection with an siRNA against GMFg for another 48 h, using Nucleofector II. .. For GMFγ overexpression studies, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with a GMFgGFP (ORIGENE) or GFP control plasmid (ORIGENE) using Nucleofector II. ..

    Over Expression:

    Article Title: Glia Maturation Factor-Gamma Regulates Autophagy and Scavenger Receptor-Mediated Phagocytosis in Murine Macrophages
    Article Snippet: For GMFγ + Nrf2 double-knockdown, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with an siRNA against Nrf2 (SR427248; ORIGENE), followed by transfection with an siRNA against GMFg for another 48 h, using Nucleofector II. .. For GMFγ overexpression studies, RAW264.7 cells (2 × 106 cells) were transiently transfected for 24 h with a GMFgGFP (ORIGENE) or GFP control plasmid (ORIGENE) using Nucleofector II. ..



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