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RNA干扰(RNAi)研究之相关工具
℡ 4000-520-616
℡ 4000-520-616
SBI/pCDH-CuO-MCS-IRES-GFP SparQ™ Cloning and Expression Lentivector/10 µg/QM530A-2-10 µg
产品编号:QM530A-2-10µg
市  场 价:¥11820.00
场      地:美国(厂家直采)
产品分类: 分子类>基因编辑>RNA干扰>
联系QQ:1570468124
电话号码:4000-520-616
邮      箱: info@ebiomall.com
美  元  价:$591.00
品      牌: SBI
公      司:System Biosciences(SBI)
公司分类:
SBI/pCDH-CuO-MCS-IRES-GFP SparQ™ Cloning and Expression Lentivector/10 µg/QM530A-2-10 µg
商品介绍

Overview

Get tight, titratable gene expression

With SBI’s SparQ™ Cumate Switch System, you can get inducible gene expression in mammalian cells with a range of cloning and expression lentivectors. The pCDH-CuO-MCS-IRES-GFP SparQ Cloning and Expression Lentivector (Cat.# QM530A-2) co-expresses both your gene- or miRNA-of-interest and the RFP marker from the inducible cumate switch promoter, enabling measurement of induction by RFP fluorescence. Co-expression is mediated by an IRES element.

With SBI’s SparQ™ Cumate Switch System, you can get inducible gene expression in mammalian cells through the binding of cumate, a non-toxic small molecule, to CymR. CymR can be delivered to cells on its own lentivector (Cat.#s QM200PA/VA-2 and QM300PA/VA-1), or on the same lentivector as your gene-of-interest (Cat.#s QM800A-1 and QM812B-1). Expression levels of your gene-of-interest are tightly controlled and increase with increasing cumate concentration until maximum induction is reached—see as much as a 32-fold increase in gene expression. Even better, induction is reversible, so you can turn expression levels on and off. Delivering negligible background expression in the absence of cumate, the SparQ System is an excellent choice for achieving controlled levels of gene expression.

  • Robust—increase expression up to 32-fold
  • Adjustable—tune expression levels by titrating the amount of cumate
  • Reversible—turn expression on, then off, then on again
  • Versatile—choose from all-in-one formats that co-express CymR and your gene-of-interest, or two-vector systems where CymR is expressed from a different plasmid
  • Powerful—suitable for in vivo applications

How It Works

Tightly-controlled, inducible gene expression

SBI’s SparQ Cumate Switch System delivers robust, titratable gene expression with low background through three components:

  • Cumate, a non-toxic, small-molecule inducer
  • CymR, a repressor that binds to cumate operator sequences in the absence of cumate
  • SparQ Lentivector that contains an MCS to clone-in your gene-of-interest, the cumate inducible promoter with cumate operator sequences (CuO) upstream of the MCS, and one or more markers

CymR has a high binding affinity for cumate and, as more cumate is added, fewer CymR molecules bind to the CuO sequences in the promoter resulting in increased expression. Exhibiting much lower background expression than similar systems, SBI’s cumate-inducible vectors can provide up to 32-fold induction of gene expression.

Supporting Data

Tight expression control with low background with the SparQ Cumate Switch System

Figure 1. Get lower background and higher induction with the SparQ Cumate Switch System than other inducible systems.

Figure 2. Gene expression with the SparQ Cumate SwitchSystem can be turned on and off, then on again.

Figure 3. Gene expression with the SparQ Cumate Switch System is titratable, with increasing amounts of cumate inducing a linear increase in gene expression.

Figure 4. With the SparQ System, gene expression can also be titrated by increasing the amount of transduced SparQ lentivirus, even up to 30 MOI.

Resources

User Manual: SparQ Cumate Switch System
Lentivirus Safety Guidelines
Product Sheet: SparQ Cumate Switch
Brochure: Gene Delivery and Expression Products and Services

Citations

  • Shinmura, K, et al. (2017) WDR62 overexpression is associated with a poor prognosis in patients with lung adenocarcinoma. Mol. Carcinog..2017 Aug 1; 56(8):1984-1991. PM ID:28277612
  • Maegawa, KI, et al. (2017) The Highly Dynamic Nature of ERdj5 Is Key to Efficient Elimination of Aberrant Protein Oligomers through ER-Associated Degradation. Structure.2017 Jun 6; 25(6):846-857.e4. PM ID:28479060
  • Park, TS, Kim, SW & Lee, JH. (2017) Efficient transgene expression system using a cumate-inducible promoter and Cre-loxP recombination in avian cells. Asian-australas. J. Anim. Sci..2017 Jun 1; 30(6):886-892. PM ID:27764912
  • Herrington, KA, et al. (2017) Spatial analysis of Cdc42 activity reveals a role for plasma membrane-associated Cdc42 in centrosome regulation. Mol. Biol. Cell.2017 May 24;. PM ID:28539409
  • Qi, Z, et al. (2017) An optimized, broadly applicable piggyBac transposon induction system. Nucleic Acids Res..2017 Apr 20; 45(7):e55. PM ID:28082389
  • Jain, A, et al. (2017) Abl kinase regulation by BRAF/ERK and cooperation with Akt in melanoma. Oncogene.2017 Apr 3;. PM ID:28368422
  • O"Hara, SP, et al. (2017) ETS Proto-oncogene 1 Transcriptionally Up-regulates the Cholangiocyte Senescence-associated Protein Cyclin-dependent Kinase Inhibitor 2A. J. Biol. Chem..2017 Mar 24; 292(12):4833-4846. PM ID:28184004
  • Ikushima, S & Boeke, JD. (2017) New Orthogonal Transcriptional Switches Derived from Tet Repressor Homologues for Saccharomyces cerevisiae Regulated by 2,4-Diacetylphloroglucinol and Other Ligands. ACS Synth Biol.2017 Mar 17; 6(3):497-506. PM ID:28005347
  • Shinmura, K, et al. (2017) Reduced expression of the DNA glycosylase gene MUTYH is associated with an increased number of somatic mutations via a reduction in the DNA repair capacity in prostate adenocarcinoma. Mol. Carcinog..2017 Feb 1; 56(2):781-788. PM ID:27253753
  • Liu, L, Huang, W & Huang, JD. (2017) Synthetic circuits that process multiple light and chemical signal inputs. BMC Syst Biol.2017 Jan 19; 11(1):5. PM ID:28103878
  • Ando, T, et al. (2017) Ameloblastin induces tumor suppressive phenotype and enhances chemosensitivity to Dox via Src-Stat3 inactivation in osteosarcoma. Sci Rep.2017 Jan 5; 7:40187. PM ID:28054649
  • Barta, T, Peskova, L & Hampl, A. (2016) miRNAsong: a web-based tool for generation and testing of miRNA sponge constructs in silico. Sci Rep.2016 Nov 18; 6:36625. PM ID:27857164
  • Choi, JS, et al. (2016) cIAPs promote the proteasomal degradation of mutant SOD1 linked to familial amyotrophic lateral sclerosis. Biochem. Biophys. Res. Commun..2016 Nov 18; 480(3):422-428. PM ID:27773815
  • Ushioda, R, et al. (2016) Redox-assisted regulation of Ca2+ homeostasis in the endoplasmic reticulum by disulfide reductase ERdj5. Proc. Natl. Acad. Sci. U.S.A..2016 Oct 11; 113(41):E6055-E6063. PM ID:27694578
  • Welti, J, et al. (2016) Analytical Validation and Clinical Qualification of a New Immunohistochemical Assay for Androgen Receptor Splice Variant-7 Protein Expression in Metastatic Castration-resistant Prostate Cancer. Eur. Urol..2016 Oct 1; 70(4):599-608. PM ID:27117751
  • Narumi, S, et al. (2016) SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7. Nat. Genet..2016 Jul 1; 48(7):792-7. PM ID:27182967
  • Park, BO, et al. (2016) Selective novel inverse agonists for human GPR43 augment GLP-1 secretion. Eur. J. Pharmacol..2016 Jan 15; 771:1-9. PM ID:26683635
  • Herrington, KA. (2016) New technologies for a better understanding of the Golgi: FLIM-FRET and click chemistry. Thesis.;. Link:Thesis
  • Shinmura, K, et al. (2015) NEIL1 p.Gln282Stop variant is predominantly localized in the cytoplasm and exhibits reduced activity in suppressing mutations. Gene.2015 Oct 15; 571(1):33-42. PM ID:26095805
  • Cheng, YS, et al. (2015) PPP2R5C Couples Hepatic Glucose and Lipid Homeostasis. PLoS Genet..2015 Oct 1; 11(10):e1005561. PM ID:26440364
Search all Citations
品牌介绍

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,提供基于慢病毒的所有相关产品、质粒、试剂盒及相关配套试剂和慢病毒延伸产品如IPS细胞多功能性诱导试剂盒和RNAi筛选文库。

SBI focuses on developing unique, innovative technologies that provide researchers with the tools to investigate and understand genomic and proteomic function. Our mission is to provide tools for the genome-wide analysis of the mechanisms that regulate cellular processes and biological responses.

Headquartered in Palo Alto about 30 miles south of San Francisco, SBI is geographically surrounded by highly successful research biotech companies (e.g., Affymetrix, Life Technologies, and Genentech) and some of the premier life science institutes in the world, including Stanford and the University of California, San Francisco.

As a small private biotechnology company, SBI capitalizes on a rich network of consultants and colleagues and continually collaborates to accelerate its development of innovative and novel applications. Currently, SBI has partnerships with over thirty scientists from several institutes.System Biosciences (SBI) consists of a highly motivated team committed to realizing the potential of its mission to develop and bring to market unique and innovative technology to investigate and understand genomic and proteomic function.

Possessing a diverse range of experience and knowledge, SBI's management and staff bring the skills, talent, and interest needed to support the company's continuing rapid growth.

A strong and proven background in creative research and product development with proficiency in genetic analysis, microarray technology, and cell biology

Extensive business development and management experience

A keen understanding of the needs of life scientists

Expertise in developing, marketing, and supporting consistent, high-quality research products

A clear focus on the need to build and maintain lasting customer relationships through support, service, and close customer interaction

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