pGreenPuro Scramble Hairpin Control (EF1α) shRNA Expression Lentivector

Streamline your shRNA studies with this ready-to-go non-targeting, scramble hairpin shRNA expression vector – co-expresses puromycin and copGFP from EF1α

Products

Catalog Number Description Size Price Quantity Add to Cart
SI506-000PA-1 pGreenPuro Scramble Hairpin Control - Construct (EF1) 10 µg $616
- +

Overview

Overview

Set up stable, heritable RNAi

Well-regarded in the industry for high, reliable gene expression, SBI’s lentiviral vectors also efficiently deliver RNAi. Generate cell lines with stable, heritable gene silencing to develop a throrough understand of the target gene’s function. Our HIV-based pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector shRNA Cloning and Expression Lentivector drives expression of your shRNA template from the H1 promoter, and after processing in the cell, your shRNA will be converted into siRNA. The vector also co-expresses puromycin and copGFP from the moderate EF1α promoter, with co-expression mediated by a T2A element.

pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector

How It Works

How It Works

Using SBI’s shRNA lentivectors to produce siRNAs

To produce siRNAs for RNAi using the pSIF1-H1-H2Kk Cloning and Expression Lentivector, first clone your shRNA template into the unique BamHI or EcoRI sites in the vector. After packaging and transduction, the vector will integrate into the genome and your shRNA will be transcribed from the H1 promoter using RNA polymerase III. The shRNA is transcribed as a single strand with a sense-loop-anti-sense structure that folds into a hairpin, and is then processed by DICER to produce an active siRNA molecule (Figure 1).

Generating siRNA from the pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector

Figure 1. Generating siRNA from the pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector.

Supporting Data

Supporting Data

Using SBI’s shRNA lentivectors—selecting for transductants

Using SBI’s shRNA lentivectors—selecting for transductants

Figure 2. Using SBI’s shRNA lentivectors. Easily select transductants with one of our markers—these examples show selection using GFP and puromycin markers on either the pSIH1-H1-copGFP (Cat.# SI501B-1) or pGreenPuro™ (Cat.# SI505A-1VB-1) shRNA Cloning and Expression Lentivectors.

FAQs

Resources

Citations

  • Wang, H, et al. (2024) TMIGD2 is an orchestrator and therapeutic target on human acute myeloid leukemia stem cells. Nature communications. 2024; 15(1):11. PM ID: 38167704
  • Jia, W, et al. (2024) Microcystin-RR promote lipid accumulation through CD36 mediated signal pathway and fatty acid uptake in HepG2 cells. Environmental Research. 2024;:118402. Link: Environmental Research
  • O'Dwyer, M, et al. (2024) PSGL-1 decorated with sialyl Lewisa/x promotes high affinity binding of myeloma cells to P-selectin but is dispensable for E-selectin engagement. Scientific reports. 2024; 14(1):1756. PM ID: 38243063
  • Deng, R, et al. (2024) PZR suppresses innate immune response to RNA viral infection by inhibiting MAVS activation in interferon signaling mediated by RIG-I and MDA5. Antiviral research. 2024; 222:105797. PM ID: 38185222
  • Yan, C, et al. (2024) PD-L1 Expression Is Increased in LPS-Induced Acute Respiratory Distress Syndrome by PI3K-AKT-Egr-1/C/EBPδ Signaling Pathway. Inflammation. 2024;. PM ID: 38376609
  • Zeng, ZC, et al. (2023) METTL3 protects METTL14 from STUB1-mediated degradation to maintain m6 A homeostasis. EMBO reports. 2023;:e55762. PM ID: 36597993
  • Sierra-Magro, A, et al. (2023) C/EBPβ Regulates TFAM Expression, Mitochondrial Function and Autophagy in Cellular Models of Parkinson’s Disease. International journal of molecular sciences. 2023; 24(2). PM ID: 36674978
  • Ma, J, et al. (2023) Enhanced E6AP-mediated ubiquitination of ENO1 via LINC00663 contributes to radiosensitivity of breast cancer by regulating mitochondrial homeostasis. Cancer Letters. 2023;:216118. Link: Cancer Letters
  • Wen, J, et al. (2023) Lnc-17Rik promotes the immunosuppressive function of Myeloid-Derived suppressive cells in esophageal cancer. Cellular immunology. 2023; 385:104676. PM ID: 36780770
  • Hasegawa, S, Imai, M & Takahashi, N. (2023) Role of acetoacetyl-CoA synthetase in glucose uptake by HepG2 cells. bioRxiv. 2023;. Link: bioRxiv
  • Agarwal, S, et al. (2023) BZW2 Inhibition Reduces Colorectal Cancer Growth and Metastasis. Molecular cancer research : MCR. 2023;:OF1-OF15. PM ID: 37067340
  • Song, S, et al. (2023) CHMP4A stimulates CD8+ T-lymphocyte infiltration and inhibits breast tumor growth via the LSD1/IFNβ axis. Cancer science. 2023;. PM ID: 37198999
  • Shaker, BT, et al. (2023) The 14-Kilodalton Human Growth Hormone Fragment a Potent Inhibitor of Angiogenesis and Tumor Metastasis. International journal of molecular sciences. 2023; 24(10). PM ID: 37240223
  • Ju, Z, et al. (2023) TXNL4B regulates radioresistance by controlling the PRP3-mediated alternative splicing of FANCI. MedComm. 2023; 4(3):e258. PM ID: 37168687
  • Salehi, S, et al. (2023) Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr. Nature communications. 2023; 14(1):4158. PM ID: 37438340
  • Zhang, B, et al. (2023) WIF1 promoter hypermethylation induce endometrial carcinogenesis through the Wnt/β-catenin signaling pathway. American journal of reproductive immunology (New York, N.Y. : 1989). 2023; 90(2):e13743. PM ID: 37491917
  • Xu, W, et al. (2023) Exosomal PIK3CB promotes PD-L1 expression and malignant transformation in esophageal squamous cell carcinoma. Medical oncology (Northwood, London, England). 2023; 40(8):221. PM ID: 37402056
  • Maruyama, M, et al. (2023) Neat1 lncRNA organizes the inflammatory gene expressions in the dorsal root ganglion in neuropathic pain caused by nerve injury. Frontiers in immunology. 2023; 14:1185322. PM ID: 37614230
  • Ma, Y, et al. (2023) The DACH1 Gene Transcriptional Activation and Protein Degradation Mediated by Transactivator Tas of Prototype Foamy Virus. Viruses. 2023; 15(9). PM ID: 37766305
  • Meng, M, et al. (2023) Eliminating the invading extracellular and intracellular FnBp+ bacteria from respiratory epithelial cells by autophagy mediated through FnBp-Fn-Integrin α5β1 axis. Frontiers in cellular and infection microbiology. 2023; 13:1324727. PM ID: 38264727
pGreenPuro Scramble Hairpin Control (EF1α) shRNA Expression Lentivector $616.00

Products

Catalog Number Description Size Price Quantity Add to Cart
SI506-000PA-1 pGreenPuro Scramble Hairpin Control - Construct (EF1) 10 µg $616
- +

Overview

Overview

Set up stable, heritable RNAi

Well-regarded in the industry for high, reliable gene expression, SBI’s lentiviral vectors also efficiently deliver RNAi. Generate cell lines with stable, heritable gene silencing to develop a throrough understand of the target gene’s function. Our HIV-based pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector shRNA Cloning and Expression Lentivector drives expression of your shRNA template from the H1 promoter, and after processing in the cell, your shRNA will be converted into siRNA. The vector also co-expresses puromycin and copGFP from the moderate EF1α promoter, with co-expression mediated by a T2A element.

pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector

How It Works

How It Works

Using SBI’s shRNA lentivectors to produce siRNAs

To produce siRNAs for RNAi using the pSIF1-H1-H2Kk Cloning and Expression Lentivector, first clone your shRNA template into the unique BamHI or EcoRI sites in the vector. After packaging and transduction, the vector will integrate into the genome and your shRNA will be transcribed from the H1 promoter using RNA polymerase III. The shRNA is transcribed as a single strand with a sense-loop-anti-sense structure that folds into a hairpin, and is then processed by DICER to produce an active siRNA molecule (Figure 1).

Generating siRNA from the pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector

Figure 1. Generating siRNA from the pGreenPuro (EF1α) shRNA Cloning and Expression Lentivector.

Supporting Data

Supporting Data

Using SBI’s shRNA lentivectors—selecting for transductants

Using SBI’s shRNA lentivectors—selecting for transductants

Figure 2. Using SBI’s shRNA lentivectors. Easily select transductants with one of our markers—these examples show selection using GFP and puromycin markers on either the pSIH1-H1-copGFP (Cat.# SI501B-1) or pGreenPuro™ (Cat.# SI505A-1VB-1) shRNA Cloning and Expression Lentivectors.

FAQs

Citations

  • Wang, H, et al. (2024) TMIGD2 is an orchestrator and therapeutic target on human acute myeloid leukemia stem cells. Nature communications. 2024; 15(1):11. PM ID: 38167704
  • Jia, W, et al. (2024) Microcystin-RR promote lipid accumulation through CD36 mediated signal pathway and fatty acid uptake in HepG2 cells. Environmental Research. 2024;:118402. Link: Environmental Research
  • O'Dwyer, M, et al. (2024) PSGL-1 decorated with sialyl Lewisa/x promotes high affinity binding of myeloma cells to P-selectin but is dispensable for E-selectin engagement. Scientific reports. 2024; 14(1):1756. PM ID: 38243063
  • Deng, R, et al. (2024) PZR suppresses innate immune response to RNA viral infection by inhibiting MAVS activation in interferon signaling mediated by RIG-I and MDA5. Antiviral research. 2024; 222:105797. PM ID: 38185222
  • Yan, C, et al. (2024) PD-L1 Expression Is Increased in LPS-Induced Acute Respiratory Distress Syndrome by PI3K-AKT-Egr-1/C/EBPδ Signaling Pathway. Inflammation. 2024;. PM ID: 38376609
  • Zeng, ZC, et al. (2023) METTL3 protects METTL14 from STUB1-mediated degradation to maintain m6 A homeostasis. EMBO reports. 2023;:e55762. PM ID: 36597993
  • Sierra-Magro, A, et al. (2023) C/EBPβ Regulates TFAM Expression, Mitochondrial Function and Autophagy in Cellular Models of Parkinson’s Disease. International journal of molecular sciences. 2023; 24(2). PM ID: 36674978
  • Ma, J, et al. (2023) Enhanced E6AP-mediated ubiquitination of ENO1 via LINC00663 contributes to radiosensitivity of breast cancer by regulating mitochondrial homeostasis. Cancer Letters. 2023;:216118. Link: Cancer Letters
  • Wen, J, et al. (2023) Lnc-17Rik promotes the immunosuppressive function of Myeloid-Derived suppressive cells in esophageal cancer. Cellular immunology. 2023; 385:104676. PM ID: 36780770
  • Hasegawa, S, Imai, M & Takahashi, N. (2023) Role of acetoacetyl-CoA synthetase in glucose uptake by HepG2 cells. bioRxiv. 2023;. Link: bioRxiv
  • Agarwal, S, et al. (2023) BZW2 Inhibition Reduces Colorectal Cancer Growth and Metastasis. Molecular cancer research : MCR. 2023;:OF1-OF15. PM ID: 37067340
  • Song, S, et al. (2023) CHMP4A stimulates CD8+ T-lymphocyte infiltration and inhibits breast tumor growth via the LSD1/IFNβ axis. Cancer science. 2023;. PM ID: 37198999
  • Shaker, BT, et al. (2023) The 14-Kilodalton Human Growth Hormone Fragment a Potent Inhibitor of Angiogenesis and Tumor Metastasis. International journal of molecular sciences. 2023; 24(10). PM ID: 37240223
  • Ju, Z, et al. (2023) TXNL4B regulates radioresistance by controlling the PRP3-mediated alternative splicing of FANCI. MedComm. 2023; 4(3):e258. PM ID: 37168687
  • Salehi, S, et al. (2023) Cytosolic Ptbp2 modulates axon growth in motoneurons through axonal localization and translation of Hnrnpr. Nature communications. 2023; 14(1):4158. PM ID: 37438340
  • Zhang, B, et al. (2023) WIF1 promoter hypermethylation induce endometrial carcinogenesis through the Wnt/β-catenin signaling pathway. American journal of reproductive immunology (New York, N.Y. : 1989). 2023; 90(2):e13743. PM ID: 37491917
  • Xu, W, et al. (2023) Exosomal PIK3CB promotes PD-L1 expression and malignant transformation in esophageal squamous cell carcinoma. Medical oncology (Northwood, London, England). 2023; 40(8):221. PM ID: 37402056
  • Maruyama, M, et al. (2023) Neat1 lncRNA organizes the inflammatory gene expressions in the dorsal root ganglion in neuropathic pain caused by nerve injury. Frontiers in immunology. 2023; 14:1185322. PM ID: 37614230
  • Ma, Y, et al. (2023) The DACH1 Gene Transcriptional Activation and Protein Degradation Mediated by Transactivator Tas of Prototype Foamy Virus. Viruses. 2023; 15(9). PM ID: 37766305
  • Meng, M, et al. (2023) Eliminating the invading extracellular and intracellular FnBp+ bacteria from respiratory epithelial cells by autophagy mediated through FnBp-Fn-Integrin α5β1 axis. Frontiers in cellular and infection microbiology. 2023; 13:1324727. PM ID: 38264727