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):
- Linearize your vector and amplify your insert using primers with at least 15 bp of homology to the ends of your linearized vector.
- Mix your PCR-amplified inserts with the linearized vector.
- Incubate for 5 minutes at room temperature and then 10 minutes on ice to fuse the insert to the linearized vector.
- 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
Resources
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