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FAQs for Nucleic Acids Technical Reference for Nucleic Acids Enzyme Finder NEBcutter NEBuffer Chart Double Digest Finder Isoschizomers DNA Sequences and Maps REBASE IMPACT-CN System pKYB1 Vector pTYB1 Vector pTYB11 Vector pTYB12 Vector pTYB2 Vector pTYB4 Vector

Home > Products > Nucleic Acids > IMPACT Vectors > pTYB3 Vector pTYB3 Vector Catalog # Size Concentration Price Qty   N6703S 10 μg 200 μg/ml $79.00 Prices are in US dollars and valid only for US orders. Download: MSDS PDF Description: pTYB3 is an E. coli expression vector (7,477 bp) used in the IMPACT™ Protein Purification System (1). This C-terminal fusion vector is designed for the in-frame insertion of a target gene into a polylinker upstream of an intein tag (the Sce VMA intein/chitin binding domain, 55 kDa) (1,2). This results in the fusion of the C-terminus of the target protein to the N-terminus of the intein tag. Thiol-induced self-cleavage of the intein releases the target protein from the chitin-bound intein tag, resulting in a single column purification of the target protein (3). For fusion of the N-terminus of the target protein to the intein tag, use pTYB11 (NEB #N6901S) or pTYB12 (NEB #N6902S). Source: pTYB3 is isolated from an E. coli strain (r? m?) by a standard plasmid purification procedure. Advantages: The NcoI site in the polylinker contains an ATG sequence for translation initiation. Use of the SapI site allows cloning of the target protein adjacent to the intein, resulting in cleavage of the target protein without any additional amino acids at its C-terminus. Unique sites are indicated in bold. Expression of the fusion gene is under the control of an IPTG-inducible T7 promoter (4). Origin of DNA replication from bacteriophage M13, which allows for the production of single-stranded DNA by helper phage superinfection of cells bearing the plasmid (M13K07 Helper Phage, NEB #N0315S). A pBR322 derivative with a ColE1 replication origin. Ampicillin resistance. T7 Universal Primer (NEB #S1248S) and Intein Reverse Primer (NEB #S1261S) are available for Sequencing the insert. Other IMPACT vectors are available which allow for fusion of a target gene to N- or C- terminus of an intein. The cleavage reaction may be induced by thiol reagent or temperature/pH shift. Companion vectors (pTYB1, pTYB2, pTYB4) differ only in the sites present in the polylinker. A wide range of E. coli host strains: ER2566 (NEB) or BL21 (DE3) and derivatives. Concentration: 200 μg/ml Storage Conditions Storage Conditions: 10 mM Tris-HCl 1 mM EDTA pH 8.0 @ 25°C Storage Temperature: -20°C Notes General notes: E. coli strain ER2566 is only available to purchasers of the IMPACT™ System or replacement vectors. References Chong, S., Mersha, F.B., Comb, D.G., Scott, M.E., Landry, D., Vence, L.M., Perler, F.B., Benner, J., Kucera, R.B., Hirvonen, C.A., Pelletier, J.J., Paulus, H. and Xu, M.-Q.  (1997) Single-column purification of free recombinant proteins using a self-cleavable affinity tag derived from a protein splicing element. Gene, 192, 271-281. Watanabe, T., Ito, Y., Yamada, T., Hashimoto, M., Sekine, S. and Tanaka, H. (1994) The role of the C-terminal domain and type III domains of chitinase A1 from Bacillus circulans WL-12 in chitin degradation. J. Bacteriol., 176, 4465-4472. Chong, S., Shao, Y., Paulus, H., Benner, J., Perler F.B. and Xu, M.-Q. (1996) Protein splicing involving the Saccharomyces, cerevisiae VMA intein: the steps in the splicing pathway, side reactions leading to protein cleavage, and establishment of an in vitro splicing system . J. Biol. Chem., 271, 22159-22168. Dubendorff, J.W. and Studier, F.W. (1991) Controlling basal expression in an inducible T7 expression system by blocking the target T7 promoter with lac repressor . J. Mol. Biol., 219, 45-59. Companion Products pKYB1 Vector pTYB1 Vector pTYB11 Vector pTYB12 Vector pTYB2 Vector pTYB4 Vector Legal Research Use Assurance: The buyer and user have a nonexclusive sublicense to use this system for any component thereof for RESEARCH PURPOSES ONLY, based upon agreement to the following assurances. Transfer of this vector in host cells that contain the cloned copy of the T7 gene 1 to third parties is explicitly prohibited. Licenses/Patents/Disclaimers: Notice to Buyer/User: the buyer/user has a non-exclusive license to use this system or any components thereof for RESEARCH PURPOSES ONLY. See Research Use Assurance Statement for details on terms of the license granted hereunder. A license to use this system or any components thereof for commercial purposes may be obtained from New England Biolabs, Inc.: Commercial Laboratory Buyer/User: Use of the vector in host cells that contain the cloned copy of T7 gene 1, the gene for T7 RNA polymerase for any purpose other than in combination with the IMPACT™ System is explicitly prohibited. Use of the host cells that contain the copy of the T7 gene 1, the gene for T7 RNA polymerase with any other vector(s) containing a T7 promoter to direct the production of RNA or protein requires a license from Brookhaven National Laboratory. Information about research-use or commercial-use license agreements may be obtained from the Office of Technology Transfer, Brookhaven National Laboratory, Building 475D, P.O. Box 5000, Upton, New York 11973-5000; Tel. 631-344-7134, Fax: 631-344-3729. You may refuse this non-exclusive research license agreement by returning the enclosed materials unused. By keeping or using the enclosed materials, you agree to be bound by the terms of this sub-license. Note: E. coli strain ER2566 is only available to purchasers of the IMPACT™ System or replacement vectors.