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70757 pET Expression System 16b - Novagen

70757
  
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      Overview

      Replacement Information
      Description
      Overview

      This product has been discontinued.





      pET Expression Systems and pET
      pET Expression Systems and pET Expression Systems plus Competent Cells provide core reagents needed for target gene cloning and expression.

      Components: pET Expression Systems
      Components for pET Expression Systems are similar for all systems unless otherwise stated with the specific pET Expression System description. pET Expression Systems include:
      • 10 µg pET vector DNA (for each indicated plasmid)
      • 0.2 ml BL21 Glycerol Stock
      • 0.2 ml BL21(DE3) Glycerol Stock
      • 0.2 ml BL21(DE3)pLysS Glycerol Stock
      • 0.2 ml Induction Control Glycerol Stock

      Components: pET Expression Systems plus Competent Cells
      pET Expression Systems plus Competent Cells contain all of the components of the specific pET Expression System, as well as the following additional components, unless otherwise stated with the specific pET Expression System description:
      • 0.2 ml NovaBlue Competent Cells
      • 0.2 ml BL21(DE3) Competent Cells
      • 0.2 ml BL21(DE3)pLysS Competent Cells
      • 2 × 0.2 ml SOC Medium
      • 10 µl Test Plasmid

      These components are sufficient for up to 10 transformations in each host.

      Purification and Detection Reagents
      Purification and detection reagents are available separately. For complete product descriptions and ordering information, refer to the Protein Purification and Antibodies, Conjugates & Detection Tools chapters.

      pET Expression System 16b
      The pET-16b vector carries an N-terminal His•Tag® sequence followed by a Factor Xa site and three cloning sites. Note that the sequence is numbered by the pBR322 convention, so the T7 expression region is reversed on the vector map, TB046VM.




      Commercial use of this Product requires a commercial license from EMD Millipore Corporation. Commercial use shall include but not be limited to (1) use of the Product or its components in manufacturing; (2) use of the Product or its components to provide a service, information, or data to others in exchange for consideration; (3) use of the Product or its components (or any derivatives thereof) for therapeutic, diagnostic or prophylactic purposes (including as part of a device, chip, assay or other product); or (4) resale of the Product or its components, whether or not such Product or its components are resold for use in research. Nothing contained herein shall be deemed to represent or warrant that additional third party rights are not required for use of this Product.

      This product contains genetically modified organisms (GMO). Within the EU GMOs are regulated by Directives 2001/18/EC and 2009/41/EC of the European Parliament and of the Council and their national implementation in the member States respectively. This legislation obliges MilliporeSigma to request certain information about you and the establishment where the GMOs are being handled. Click here for Enduser Declaration (EUD) Form.
      Catalogue Number70757
      Brand Family Novagen®
      References
      Product Information
      Components
      Fusion tagHis•Tag
      Applications
      Biological Information
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Shipped with Blue Ice or with Dry Ice
      Toxicity Standard Handling
      Storage ≤ -70°C
      Avoid freeze/thaw Avoid freeze/thaw
      Do not freeze Ok to freeze
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Catalogue Number GTIN
      70757 0

      Documentation

      pET Expression System 16b - Novagen Certificates of Analysis

      TitleLot Number
      70757

      Citations

      Title
    • Franca Rossi, et al. (2008) Crystal structure of human kynurenine aminotransferase II, a drug target for the treatment of Schizophrenia. Journal of Biological Chemistry 283, 3559-3566.
    • Nadine Kröning, et al. (2007) ATP binding to the KTN/RCK subunit KtrA from the K+-uptake system KtrAB of Vibrio alginolyticus: Its role in the formation of the KtrAB complex and its requirement in vivo. Journal of Biological Chemistry 282, 14018-14027.
    • Michele M. Otte, Jesse D. Woodson and Jorge C. Escalante-Semerena. (2007) The thiamine kinase (YcfN) enzyme plays a minor but significant role in cobinamide salvaging in Salmonella enterica. Journal of Bacteriology 189, 7310-7315.
    • Pascale Plamondon, Nicole R. Luke and Anthony A. Campagnari. (2007) Identification of a novel two-partner secretion locus in Moraxella catarrhalis. Infection and Immunity 75, 2929-2936.
    • Krishna Murari Sinha, et al. (2007) Mycobacterial UvrD1 is a ku-dependent DNA helicase that plays a role in multiple DNA repair events, including double-strand break repair. Journal of Biological Chemistry 282, 15114-15125.
    • Zhong Yu, et al. (2007) The protein that binds to DNA base J in trypanosomatids has features of a thymidine hydroxylase. Nucleic Acids Research 35, 2107-2115.
    • Claudia Colasante, et al. (2006) Characterization and developmentally regulated localization of the mitochondrial carrier protein homologue MCP6 from Trypanosoma brucei. Eukaryotic Cell 5, 1194-1205.
    • Mieke F. Roelofs, et al. (2006) Identification of small heat shock protein B8 (HSP22) as a novel TLR4 ligand and potential involvement in the pathogenesis of rheumatoid arthritis. Journal of Immunology 176, 7021-7027.
    • Hiroyuki Ashida, Yoshihiro Sawa and Hitoshi Shibata. (2005) Cloning, biochemical and phylogenetic characterizations of γ-glutamylcysteine synthetase from Anabaena sp. PCC 7120. Plant and Cell Physiology 46, 557-562.
    • Peter T. Beernink, et al. (2005) Specificity of protein interactions mediated by BRCT domains of the XRCC1 DNA repair protein. Journal of Biological Chemistry 280, 30206-30213.
    • Nobutaka Funa, et al. (2005) A novel quinone-forming monooxygenase family involved in modification of aromatic polyketides. Journal of Biological Chemistry 280, 14514-14523.
    • Boris Hambsch, et al. (2005) γ-Protocadherins: presenilin-mediated release of C-terminal fragment promotes locus expression. Journal of Biological Chemistry 280, 15888-15897.
    • Takashi Iwata, et al. (2005) Frequent immune responses to a cancer/testis antigen, CAGE, in patients with microsatellite instability-positive endometrial cancer. Clinical Cancer Research 11, 3949-3957.
    • Alla Korepanova, et al. (2005) Cloning and expression of multiple integral membrane proteins from Mycobacterium tuberculosis in Escherichia coli. Protein Science 14, 148-158.
    • Dong Liu, et al. (2005) Human homologue of cement gland protein, a novel metastasis inducer associated with breast carcinomas. Cancer Research 65, 3796-3805.
    • Peter J. O'Brien, et al. (2005) The novel apolipoprotein A5 is present in human serum, is associated with VLDL, HDL, and chylomicrons, and circulates at very low concentrations compared with other apolipoproteins. Clinical Chemistry 51, 351-359.
    • Annabelle Varrot, et al. (2005) Mycobacterium tuberculosis strains possess functional cellulases. Journal of Biological Chemistry 280, 20181-20184.
    • Adam Wilkinson, et al. (2005) Analysis of ligation and DNA binding by Escherichia coli DNA ligase (LigA). Biochimica et Biophysica Acta 1749, 113-122.
    • Xiansi Zhao, et al. (2005) Apoptosis factor EI24/PIG8 is a novel endoplasmic reticulum-localized Bcl-2-binding protein which is associated with suppression of breast cancer invasiveness. Cancer Research 65, 2125-2129.
    • Hui Zhu and Stewart Shuman. (2005) A primer-dependent polymerase function of Pseudomonas aeruginosa ATP-dependent DNA ligase (LigD). Journal of Biological Chemistry 280, 418-427.
    • Simon R. Andrews, et al. (2004) The use of forced protein evolution to investigate and improve stability of family 10 Xylanases: the production of Ca2+-independent stable xylanases. Journal of Biological Chemistry 279, 54369-54379.
    • Daisuke Kobayashi, et al. (2003) Molecular characterization and redox regulation of phosphoribulokinase from the cyanobacterium Synechococcus sp. PCC 7942. Plant and Cell Physiology 44, 269-276.
    • Kaisa Huhtinen, et al. (2002) The peroxisome proliferator-induced cytosolic type I acyl-CoA thioesterase (CTE-I) is a serine-histidine-aspartic acid α/β hydrolase. Journal of Biological Chemistry 277, 3424-3432.
    • N. Funa, et al. (1999) A new pathway for polyketide synthesis in microorganisms. 400, 897-899.
    • Ning Zheng and Lila M. Gierasch. (1997) Domain interactions in E. coli SRP: Stabilization of M domain by RNA is required for effective signal sequence modulation of NG domain. Molecular Cell 1, 79-87.
    • Quinn Deveraux, Chris Jensen and Martin Rechsteiner. (1995) Molecular cloning and expression of a 26S protease subunit enriched in dileucine repeats. Journal of Biological Chemistry 270, 23726-23729.
    • Olivia C. Ong, et al. (1995) Molecular cloning and characterization of the G protein γ subunit of cone photoreceptors. Journal of Biological Chemistry 270, 8495-8500.
    • Yukiko Gotoh, et al. (1994) Characterization of recombinant Xenopus MAP kinase kinases mutated at potential phosphorylation sites. Oncogene 9, 1891-1898.
    • C.A. Franke and D.E. Hruby. (1993) Expression and single-step purification of enzymatically active vaccinia virus thymidine kinase containing an engineered oligohistidine domain by immobilized metal affinity chromatography.. Protein Expression and Purification 4, 101-109.
    • User Protocols

      Title
      TB053 Academic and Non-profit Laboratory Assurance Letter
      TB055 pET System Manual

      Vector Map

      Title
      TB046VM pET-16b Vector Map

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