4000-520-616
欢迎来到免疫在线!(蚂蚁淘生物旗下平台)  请登录 |  免费注册 |  询价篮
System Biosciences(授权代理)
主营:RNA干扰(RNAi)研究之相关工具
咨询热线电话
4000-520-616
当前位置: 首页 > 产品中心 > juhewu > SBI/PB-CMV-GreenPuro-H1-MCS shRNA克隆和表达载体/10µg/PBSI505A-1-10µg
商品详细SBI/PB-CMV-GreenPuro-H1-MCS shRNA克隆和表达载体/10µg/PBSI505A-1-10µg
SBI/PB-CMV-GreenPuro-H1-MCS shRNA克隆和表达载体/10µg/PBSI505A-1-10µg
SBI/PB-CMV-GreenPuro-H1-MCS shRNA克隆和表达载体/10µg/PBSI505A-1-10µg
商品编号: PBSI505A-1-10µg
品牌: System Biosciences
市场价: ¥12240.00
美元价: 7344.00
产地: 美国(厂家直采)
公司:
产品分类: 聚合物
公司分类: juhewu
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

Overview

Easy and consistent shRNA delivery and expression

Not just for genes, the PiggyBac system is also an excellent choice for reliably producing shRNA. The PB-CMV-GreenPuro-H1-MCS shRNA Cloning and Expression Vector (Cat.# PBSI505A-1) drives production of your shRNA from the strong H1 promoter. The vector also features GFP and puromycin resistance co-expressed from the strong CMV promoter, with co-expression mediated by the T2A element.

With the PiggyBac Transposon System, you can:

  • Make transgenic cell lines with a single transfection
  • Integrate multiple PiggyBac Vectors in a single transfection
  • Insert an expression cassette into human, mouse, and rat cells
  • Deliver virtually any-sized DNA insert, from 10 – 100 kb
  • Choose from PiggyBac Vectors that express your gene-of-interest from constitutive or inducible promoters and include a variety of markers
  • Determine the number of integration events with the PiggyBac qPCR Copy Number Kit (# PBC100A-1)

Customer AgreementsAcademic customers can purchase PiggyBac Transposon System components for internal research purposes for indefinite use, whereas commercial customers must sign a customer agreement for a four-month, limited-use license to evaluate the technology.For end user license information, see the following:

  • Academic Customers—End-User License Information
  • Commercial Customers—End-User License Information

* SBI is fully licensed to distribute PiggyBac vectors as a partnership with Hera BioLabs, Inc.

How It Works

The PiggyBac Transposon System’s Cut-and-Paste Mechanism

The efficient PiggyBac Transposon System uses a cut-and-paste mechanism to transfer DNA from the PiggyBac Vector into the genome. If only temporary genomic integration is desired, the Excision-only PiggyBac Transposase can be transiently expressed for footprint-free removal of the insert, resulting in reconstitution of the original genome sequence.

Figure 1. The PiggyBac Transposon System’s cut-and-paste mechanism.

  • The Super PiggyBac Transposase binds to specific inverted terminal repeats (ITRs) in the PiggyBac Cloning and Expression Vector and excises the ITRs and intervening DNA.
  • The Super PiggyBac Transposase inserts the ITR-Expression Cassette-ITR segment into the genome at TTAA sites.
  • The Excision-only Super PiggyBac Transposase can be used to remove the ITR-Expression Cassette-ITR segment from the genome, for footprint-free removal

Resources

User Manual: PiggyBac Transposon System
Product Sheet: PiggyBac Transposon System
Brochure: Gene Delivery and Expression Products and Services

Citations

  • Schertzer, MD, et al. (2019) lncRNA-Induced Spread of Polycomb Controlled by Genome Architecture, RNA Abundance, and CpG Island DNA. Mol. Cell.2019 Jun 27;. PM ID:31256989
  • Denes, LT, et al. (2019) Culturing C2C12 myotubes on micromolded gelatin hydrogels accelerates myotube maturation. Skelet Muscle.2019 Jun 7; 9(1):17. PM ID:31174599
  • Richter, JF, et al. (2019) Occludin knockdown is not sufficient to induce transepithelial macromolecule passage. Tissue Barriers.2019 Jun 4; 7(2):1612661. PM ID:31161924
  • Mao, X, et al. (2019) Schedule-dependent potentiation of chemotherapy drugs by the hypoxia-activated prodrug SN30000. Cancer Biol. Ther..2019 May 26;:1-12. PM ID:31131698
  • Chapnick, DA, et al. (2019) Temporal Metabolite, Ion, and Enzyme Activity Profiling Using Fluorescence Microscopy and Genetically Encoded Biosensors. Methods Mol. Biol..2019 May 24; 1978:343-353. PM ID:31119673
  • Shinmura, K, et al. (2019) POLQ Overexpression Is Associated with an Increased Somatic Mutation Load and PLK4 Overexpression in Lung Adenocarcinoma. Cancers (Basel).2019 May 24; 11(5). PM ID:31137743
  • Li, F, et al. (2019) A piggyBac-based TANGO GFP assay for high throughput screening of GPCR ligands in live cells. Cell Commun. Signal.2019 May 23; 17(1):49. PM ID:31122241
  • Shrestha, M, et al. (2019) The transition of tissue inhibitor of metalloproteinases from -4 to -1 induces aggressive behavior and poor patient survival in dedifferentiated liposarcoma via YAP/TAZ activation. Carcinogenesis.2019 May 10;. PM ID:31074490
  • Gan, L, et al. (2019) The lysosomal GPCR-like protein GPR137B regulates Rag and mTORC1 localization and activity. Nat. Cell Biol..2019 May 1; 21(5):614-626. PM ID:31036939
  • Ahmad, ST, et al. (2019) Capicua regulates neural stem cell proliferation and lineage specification through control of Ets factors. Nat Commun.2019 May 1; 10(1):2000. PM ID:31043608
  • Rivera, FJ, et al. (2019) Aging restricts the ability of mesenchymal stem cells to promote the generation of oligodendrocytes during remyelination. Glia.2019 Apr 30;. PM ID:31038798
  • Inoue, M, et al. (2019) Structural Basis of Sarco/Endoplasmic Reticulum Ca2+-ATPase 2b Regulation via Transmembrane Helix Interplay. Cell Rep.2019 Apr 23; 27(4):1221-1230.e3. PM ID:31018135
  • Bielczyk-Maczyńska, E, et al. (2019) Loss of adipocyte identity through synergistic repression of PPARγ by TGF-β and mechanical stress. bioRxiv.2019 Apr 11;. Link:bioRxiv
  • Paydarnia, N, et al. (2019) Synergistic effect of granzyme B-azurin fusion protein on breast cancer cells. Mol. Biol. Rep..2019 Apr 1;. PM ID:30937652
  • Sakahara, M, et al. (2019) IFN/STAT signaling controls tumorigenesis and the drug response in colorectal cancer. Cancer Sci..2019 Apr 1; 110(4):1293-1305. PM ID:30724425
  • Jones, EM, et al. (2019) A Scalable, Multiplexed Assay for Decoding GPCR-Ligand Interactions with RNA Sequencing. Cell Syst.2019 Mar 27; 8(3):254-260.e6. PM ID:30904378
  • Sauter, EJ, et al. (2019) Induced Neurons for the Study of Neurodegenerative and Neurodevelopmental Disorders. Methods Mol. Biol..2019 Mar 23; 1942:101-121. PM ID:30900179
  • Laugsch, M, et al. (2019) Modeling the Pathological Long-Range Regulatory Effects of Human Structural Variation with Patient-Specific hiPSCs. Cell Stem Cell.2019 Mar 21;. PM ID:30982769
  • Farhadi, A, et al. (2019) Ultrasound Imaging of Gene Expression in Mammalian Cells. bioRxiv.2019 Mar 18;. Link:bioRxiv
  • Garivet, G, et al. (2019) Small-Molecule Inhibition of the UNC-Src Interaction Impairs Dynamic Src Localization in Cells. Cell Chem Biol.2019 Mar 13;. PM ID:30956149
Search all Citations
品牌介绍
美国SBI代理 System Biosciences,简称SBI,美国加州湾区新成立的生技公司,致力于独特、创新生物技术之开发,以研发利于基因及蛋白质功能鉴定、研究之崭新方法和工具为宗旨。 现阶段研发重心为RNA干扰(RNAi)研究之相关工具。 System Biosciences (SBI) 致力于开发独特、革新的技术,为客户研究蛋白组学和基因组学功能提供研究工具。SBI 是专业的慢病毒产品公司,提供基于慢病毒 美国SBI代理 ExoQuick and ExoQuick-TC Products Product Size Catalog # ExoQuick serum exosome precipitation solution (5 ml) 75 reactions EXOQ5A-1 ExoQuick Plasma prep and Exosome precipitation kit (5 ml ExoQuick plus 500 ul Thrombin at 500U/mL), replaces EXOQ5TD-1 product 75 reactions EXOQ5TM-1 Thrombin Plasma prep for Exosome precipitation (500 ul at 500U/mL), replaces TDEXO-1 product 100 reactions TMEXO-1 ExoQuick serum exosome precipitation solution (20 ml) 300 reactions EXOQ20A-1 ExoQuick-TC for Tissue Culture Media and Urine (10ml) 10 reactions EXOTC10A-1 ExoQuick-TC for Tissue Culture Media and Urine (50ml) 50 reactions EXOTC50A-1 Exosome-depleted FBS Media Supplement - USA Certified 50 ml EXO-FBS-50A-1 Exosome-depleted FBS Media Supplement - USA Certified 250 ml EXO-FBS-250A-1 ExoQuick-LP Lipoprotein Pre-Clear & Exosome Precipitation Kit 5 reactions EXOLP5A-1
联络我们
服务热线:4000-520-616
(限工作日9:00-18:00)
QQ :1570468124
手机:18915418616