pLenti-III-mir-GFP Control Vector

Cat. No.
m001
Unit
500 ng
Price
$185.00
Cat. No. m001
Name pLenti-III-mir-GFP Control Vector
Unit 500 ng
Category Control Vectors & Viruses
Description

This miRNA lentiviral vector is part of abm’s Lentivirus Expression System and can be packaged into virus using an appropriate packaging mix to over-express your miRNA of interest in a wide range of host cells or animal models. This construct cont

Vector Map pLenti-III-mir-GFP-Blank (click blue link to view)
Storage Condition

Store at -20°C or below upon receipt

Material Citation If use of this material results in a scientific publication, please cite the material in the following manner: Applied Biological Materials Inc, Cat. No. m001
Print & Download Datasheet
  • Xin, H et al. " MiR-133b Promotes Neural Plasticity and Functional Recovery After Treatment of Stroke with Multipotent Mesenchymal Stromal Cells in Rats Via Transfer of Exosome-Enriched Extracellular Particles" STEM CELLS 31:2737-2746 (2013). DOI: 10.1002/stem.1409. Application: miRNA control vector.
  • He, Q;Zhou, X;Li, S;Jin, Y;Chen, Z;Chen, D;Cai, Y;Liu, Z;Zhao, T;Wang, A;, et al. "MicroRNA-181a suppresses salivary adenoid cystic carcinoma metastasis by targeting MAPK-Snai2 pathway" Biochim. Biophys. Acta 1830-11:5258-66 (2013). PubMed: 23911747.
  • Bibikova, E et al. "Identification of Novel Pathways in the Pathogenesis of Diamond-Blackfan Anemia" Thesis : (0). Application: miRNA Expression Control.
  • Sun, Y et al. "Reduced miR-3127-5p expression promotes NSCLC proliferation/invasion and contributes to dasatinib sensitivity via the c-Abl/Ras/ERK pathway" Sci. Rep 4:6527 (2014). DOI: 10.1038/srep06527. PubMed: 25284075. Application: Control Vector.
  • Chopp, M et al. "MiR-133b Promotes Neural Plasticity and Functional Recovery After Treatment of Stroke with Multipotent Mesenchymal Stromal Cells in Rats Via Transfer of Exosome-Enriched Extracellular Particles" AlphaMed Press 12:2737-2746 (2013). DOI: 10.1002/stem.1409. Application: microRNA.
  • Zhao, G et al. ""miR-203 Functions as a Tumor Suppressor by Inhibiting Epithelial to Mesenchymal Transition in Ovarian Cancer"" J Cancer Sci Thr 2:34-43 (2015). DOI: 10.4172/1948-5956.1000322.
  • Jafarian, A et al. "The Generation of Insulin Producing Cells from Human Mesenchymal Stem Cells by MiR-375 and Anti-MiR-9" PLoS One 6: (2015). DOI: 10.1371/journal.pone.0128650. PubMed: 26047014.
  • Sendi, H et al. "miR-122 decreases HCV entry into hepatocytes through binding to the 3′ UTR of OCLN mRNA" Liver Int 6:1315-1323 (2015). DOI: 10.1111/liv.12698.
  • Pajoohesh, M et al. "MicroRNA-145-based differentiation of human mesenchymal stem cells to smooth muscle cells" Biotechnol. Lett 38.11:1975 (2016). DOI: 10.1007/s10529-016-2177-1. Application: Lentiviral production.
  • Ding, et al. "MicroRNA-585 acts as a tumor suppressor in non-small-cell lung cancer by targeting hSMG-1" Clinical and Translational Oncology 2016:1 (2016). DOI: 10.1007/s12094-016-1562-5. Application: Cloning.
  • Kobayashi, M., Benakis, C., Anderson, C., Moore, M. J., Poon, C., Uekawa, K., … Darnell, R. B. "AGO CLIP Reveals an Activated Network for Acute Regulation of Brain Glutamate Homeostasis in Ischemic Stroke" Cell Reports 28(4):979–991.e6 (2019). DOI: 10.1016/j.celrep.2019.06.075.
  • Lu, Y., Huang, W., Chen, H., Wei, H., Luo, A., Xia, G., Deng, X., Zhang, G. "MicroRNA-224, negatively regulated by c-jun, inhibits growth and epithelial-to-mesenchymal transition phenotype via targeting ADAM17 in oral squamous cell carcinoma" Journal of cellular an dmolecular medicine 23(8):4913-4920 (2019). DOI: 10.1111/jcmm.14107.
  • Lu., Yaoyong., . "“MicroRNA‐224, Negatively Regulated by c‐Jun, Inhibits Growth and Epithelial‐to‐Mesenchymal Transition Phenotype via Targeting ADAM17 in Oral Squamous Cell Carcinoma”" Journal of Cellular and Molecular Medicine vol. 23:no. 8 (2019). DOI: 10.1111/jcmm.14107..
  • Zhang, H., Jiang, S., Guo, L., & Li, X. "MicroRNA‐1258, regulated by c‐Myb, inhibits growth and epithelial‐to‐mesenchymal transition phenotype via targeting SP1 in oral squamous cell carcinoma" Journal of Cellular and Molecular Medicine 23(4):2813–2821 (2019). DOI: 10.1111/jcmm.14189.
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