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/带活性细胞的冷融合克隆试剂盒/10反应/MC010B-1-10反应
商品详细SBI/带活性细胞的冷融合克隆试剂盒/10反应/MC010B-1-10反应
SBI/带活性细胞的冷融合克隆试剂盒/10反应/MC010B-1-10反应
SBI/带活性细胞的冷融合克隆试剂盒/10反应/MC010B-1-10反应
商品编号: MC010B-1-10Reactions
品牌: System Biosciences
市场价: ¥4820.00
美元价: 2892.00
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

Quick and easy ligation-free cloning

Fast, easy, and efficient, SBI’s Cold Fusion Cloning is an excellent choice for any cloning project. Whether you’re assembling multiple fragments of DNA or simply adding an insert or gBlock® to a vector, the Cold Fusion Cloning Kit will take you to transformation-ready DNA in a single step—just incubate your DNA fragment(s) with linearized vector for five minutes at room temperature and ten minutes on ice. A typical cloning reaction will deliver a successful cloning rate of more than 90%.

  • Fast—get transformation-ready DNA in as little as twenty minutes
  • Easy—a phosphatase-free and ligation-free system that eliminates the need for specific restriction enzymes
  • Efficient—typically achieve >90% positive clones
  • Versatile—add any insert into any site in any vector using manual or automated workflows

“I have designed and made hundreds and hundreds of clones using the traditional and not so traditional methods since I started doing research. I must say the Cold Fusion kit makes it way too easy to design a vector or new construct—it’s a really good product.”

~Hidevaldo B. Machado, PhD., UCLA

How It Works

Streamlining vector construction with Cold Fusion Cloning

Cold Fusion Cloning is a quick and easy way to place an insert—or multiple inserts simultaneously—into a linearized vector. The Cold Fusion Master mix contains a proprietary blend of enzymes that prepares DNA fragments ends for sequence-directed alignment. Homologous DNA ends are efficiently fused together and produce vector clones with great accuracy.

The four-step process is as follows (see workflow illustration below):

  1. Linearize your vector and amplify your insert using primers with at least 15 bp of homology to the ends of your linearized vector.
  2. Mix your PCR-amplified inserts with the linearized vector.
  3. Incubate for 5 minutes at room temperature and then 10 minutes on ice to fuse the insert to the linearized vector.
  4. Transform competent cells with the fusion mix. A typical Cold Fusion Cloning reaction delivers 90% positive clones.

Supporting Data

See the results of a better way to clone

Figure 1. Cold Fusion Cloning can clone 3′, 5′, and blunt-end fragments efficiently.

Figure 2. Simultaneously insert multiple fragments into a vector in a defined order. Using Cold Fusion technology, the team at SBI built a 4-in-1 construct to generate iPSCs in only three days.

Resources

User Manual: Cold Fusion Cloning
Protocol: Cold Fusion Cloning
Product Sheet: Cold Fusion Cloning Kit
Brochure: Gene Delivery and Expression Products and Services

Citations

  • Lamborn, IT, et al. (2017) Recurrent rhinovirus infections in a child with inherited MDA5 deficiency. J. Exp. Med..2017 Jul 3; 214(7):1949-1972. PM ID:28606988
  • Verhelle, A, et al. (2017) AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model.. Hum. Mol. Genet..2017 Jun 9;. PM ID:28605435
  • Bardwell, AJ, et al. (2017) The WW domain of the scaffolding protein IQGAP1 is neither necessary nor sufficient for binding to the MAPKs ERK1 and ERK2. J. Biol. Chem..2017 May 26; 292(21):8750-8761. PM ID:28396345
  • 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
  • Tidd, N, et al. (2017) Minicircle Mediated Gene Delivery to Canine and Equine Mesenchymal Stem Cells. Int J Mol Sci.2017 Apr 12; 18(4). PM ID:28417917
  • Sathyan, KM, Fachinetti, D & Foltz, DR. (2017) α-amino trimethylation of CENP-A by NRMT is required for full recruitment of the centromere. Nat Commun.2017 Mar 7; 8:14678. PM ID:28266506
  • Hattori, A, et al. (2017) RNA binding protein MSI2 positively regulates FLT3 expression in myeloid leukemia. Leuk. Res..2017 Mar 1; 54:47-54. PM ID:28107692
  • Yuan, Y, et al. (2017) The molecular basis of talin2’s high affinity toward β1-integrin. Sci Rep.2017 Feb 3; 7:41989. PM ID:28155884
  • Gieseler-Halbach, S, et al. (2017) RSK-mediated nuclear accumulation of the cold-shock Y-box protein-1 controls proliferation of T cells and T-ALL blasts. Cell Death Differ..2017 Feb 1; 24(2):371-383. PM ID:28009354
  • Dauden, MI, et al. (2017) Architecture of the yeast Elongator complex.. EMBO Rep..2017 Feb 1; 18(2):264-279. PM ID:27974378
  • Sugiyama, H, et al. (2017) Nat1 promotes translation of specific proteins that induce differentiation of mouse embryonic stem cells. Proc. Natl. Acad. Sci. U.S.A..2017 Jan 10; 114(2):340-345. PM ID:28003464
  • Brett, E, et al. (2017) Magnetic Nanoparticle-Based Upregulation of B-Cell Lymphoma 2 Enhances Bone Regeneration. Stem Cells Transl Med.2017 Jan 1; 6(1):151-160. PM ID:28170185
  • Chen, B, et al. (2016) ERK-mediated NF-κB activation through ASIC1 in response to acidosis. Oncogenesis.2016 Dec 12; 5(12):e279. PM ID:27941930
  • Jiménez-Amilburu, V, et al. (2016) In Vivo Visualization of Cardiomyocyte Apicobasal Polarity Reveals Epithelial to Mesenchymal-like Transition during Cardiac Trabeculation. Cell Rep.2016 Dec 6; 17(10):2687-2699. PM ID:27926871
  • Verhelle, A, et al. (2016) Non-Invasive Imaging of Amyloid Deposits in a Mouse Model of AGel Using (99m)Tc-Modified Nanobodies and SPECT/CT.. Mol Imaging Biol.2016 Dec 1; 18(6):887-897. PM ID:27130233
  • Martínez-Barricarte, R, et al. (2016) Transduction of Herpesvirus saimiri-Transformed T Cells with Exogenous Genes of Interest. Curr Protoc Immunol.2016 Nov 1; 115:7.21C.1-7.21C.12. PM ID:27801513
  • Sprowl-Tanio, S, et al. (2016) Lactate/pyruvate transporter MCT-1 is a direct Wnt target that confers sensitivity to 3-bromopyruvate in colon cancer. Cancer Metab.2016 Oct 12; 4:20. PM ID:27729975
  • Qi, L, et al. (2016) Talin2-mediated traction force drives matrix degradation and cell invasion. J. Cell. Sci..2016 Oct 1; 129(19):3661-3674. PM ID:27694340
  • Lin, B, et al. (2016) The protective role of p72 in doxorubicin‑induced cardiomyocytes injury in vitro. Mol Med Rep.2016 Oct 1; 14(4):3376-80. PM ID:27510756
  • Dincer, E, et al. (2016) Canine Infections and Partial S Segment Sequence Analysis of Toscana Virus in Turkey. Vector Borne Zoonotic Dis..2016 Sep 1; 16(9):611-8. PM ID:27400226
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