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70777 pET Expression System 28 - Novagen

pET vectors plus host strains with induction control

pET Expression System 28 - Novagen MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
70777
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Overview

Replacement Information

Products

Catalogue NumberPackaging Qty/Pack
70777-3 Sklená flaša 1 ea
Description
OverviewpET 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 28
The pET Expression System 28 contains 10 µg each of the four versions of pET-28 (pET-28a–c(+)). The pET-28a–c(+) vectors carry an N-terminal His•Tag®/thrombin/T7•Tag® configuration plus an optional C-terminal His•Tag sequence. Note that the sequence is numbered by the pBR322 convention, so the T7 expression region is reversed on the vector map, TB074VM.




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 Number70777
Brand Family Novagen®
References
Product Information
•10 µg eachpET-28a-c(+) vector DNA
•0.2 mlHost bacterial strains BL21, BL21(DE3), and BL21(DE3)pLysS, glycerol stocks
•0.2 mlInduction control clone, glycerol stock
Fusion tagHis•Tag, T7•Tag
Quality LevelMQ100
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
70777-3 04055977273205

Documentation

pET Expression System 28 - Novagen Certificates of Analysis

TitleLot Number
70777

Citations

Title
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  • Brian P. Anton, et al. (2008) RimO, a MiaB-like enzyme, methylthiolates the universally conserved Asp88 residue of ribosomal protein S12 in Escherichia coli. Procedings of the National Academy of Science 105, 1826-1831.
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  • Jennifer L. Farmer, et al. (2008) Galectin 15 (LGALS15) functions in trophectoderm migration and attachment. Federation of American Societies for Experimental Biology Journal 22, 548-560.
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  • Bidyottam Mittra, et al. (2008) The TbMTr1 spliced leader RNA cap 1 2 '-O-Ribose methyltransferase from Trypanosoma brucei acts with substrate specificity. Journal of Biological Chemistry 283, 3161-3172.
  • Sunish Kumar Radhakrishnan, Martin Thanbichler and Patrick H. Viollier. (2008) The dynamic interplay between a cell fate determinant and a lysozyme homolog drives the asymmetric division cycle of Caulobacter crescentus. Genes and Development 22, 212-225.
  • A. Reza Radjabi, et al. (2008) Thrombin induces tumor invasion through the induction and association of matrix metalloproteinase-9 and 1-integrin on the cell surface. Journal of Biological Chemistry 283, 2822-2834.
  • Dashuang Shi, et al. (2008) The crystal structure of N-acetyl-L-glutamate synthase from Neisseria gonorrhoeae provides insights into mechanisms of catalysis and regulation. Journal of Biological Chemistry 283, 7176-7184.
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  • Antonella Antignani and Richard J. Youle. (2007) The cytokine, granulocyte-macrophage colony-stimulating factor (GM-CSF), can deliver Bcl-XL as an extracellular fusion protein to protect cells from apoptosis and retain differentiation induction. Journal of Biological Chemistry 282, 11246-11254.
  • Carol S. Baker, et al. (2007) CsrA inhibits translation initiation of Escherichia coli hfq by binding to a single site overlapping the Shine-Dalgarno sequence. Journal of Bacteriology 189, 5472-5481.
  • Priscilla Braglia, et al. (2007) Requirement of Nhp6 proteins for transcription of a subset of tRNA genes and heterochromatin barrier function in Saccharomyces cerevisiae. Molecular and Cellular Biology 27, 1545-1557.
  • Nicholas E. Burgis and Richard P. Cunningham. (2007) Substrate specificity of RdgB protein, a deoxyribonucleoside triphosphate pyrophosphohydrolase. Journal of Biological Chemistry 282, 3531-3538.
  • Elena Curti, Stephen J. Smerdon and Elaine O. Davis. (2007) Characterization of the helicase activity and substrate specificity of Mycobacterium tuberculosis UvrD. Journal of Bacteriology 189, 1542-1555.
  • Michael A. Fischbach, et al. (2007) Directed evolution can rapidly improve the activity of chimeric assembly-line enzymes. Procedings of the National Academy of Science 104, 11951-11956.
  • Daphna Frenkiel-Krispin, et al. (2007) Plant transformation by Agrobacterium tumefaciens: modulation of single-stranded DNA-Vir2 complex assembly by VirE1. Journal of Biological Chemistry 282, 3458-3464.
  • Vanessa Gonzalez-Covarrubias, et al. (2007) A functional genetic polymorphism on human carbonyl reductase 1 (CBR1) impacts on catalytic activity and NADPH binding affinity.. Drug Metabolism and Disposition 35, 973-980.
  • Changhui Guan, et al. (2007) Signal mimics derived from a metagenomic analysis of the gypsy moth gut microbiota. Applied and Enviornmental Microbiology 73, 3669-3676.
  • Bei Han, et al. (2007) Molecular characterization of a glucokinase with broad hexose specificity from Bacillus sphaericus strain C3-41. Applied and Enviornmental Microbiology 73, 3581-3586.
  • Marcel Hohl, et al. (2007) Domain swapping between FEN-1 and XPG defines regions in XPG that mediate nucleotide excision repair activity and substrate specificity. Nucleic Acids Research 35, 3053-3063.
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  • Marie Johansson, et al. (2007) Activation of endosomal dynein motors by stepwise assembly of Rab7-RILP-p150Glued, ORP1L, and the receptor ßlll spectrin. Journal of Cell Biology 176, 459-471.
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  • 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.
  • Ferdinand Steinboeck, et al. (2007) The nuclear actin-related protein of Saccharomyces cerevisiae, Arp4, directly Interacts with the histone acetyltransferase Esa1p. Journal of Biochemistry (Tokyo) 141, 661-668.
  • Keith A. Stubbs, et al. (2007) Small molecule inhibitors of a glycoside hydrolase attenuate inducible AmpC mediated β-lactam resistance. Journal of Biological Chemistry 282, 21382-21391.
  • Ken-ichiro Taoka, et al. (2007) Reciprocal phosphorylation and glycosylation recognition motifs control NCAPP1 interaction with pumpkin phloem proteins and their cell-to-cell movement. Plant Cell 19, 1866-1884.
  • Susanne Textor, et al. (2007) MAM3 catalyzes the formation of all Aliphatic glucosinolate chain lengths in Arabidopsis. Plant Physiology 144, 60-71.
  • Giuseppe D. Tocchini-Valentini, Paolo Fruscoloni and Glauco P. Tocchini-Valentini. (2007) The dawn of dominance by the mature domain in tRNA splicing. Procedings of the National Academy of Science 104, 12300-12305.
  • Daqi Tu, et al. (2007) Structure and function of the yeast U-box-containing ubiquitin ligase Ufd2p. Procedings of the National Academy of Science 104, 15599-15606.
  • Spencer M. Whitney and Robert E. Sharwood. (2007) Linked rubisco subunits can assemble into functional oligomers without impeding catalytic performance. Journal of Biological Chemistry 282, 3809-3818.
  • Alexander T. H. Wu, et al. (2007) PAWP, a sperm specific WW-domain binding protein, promotes meiotic resumption and pronuclear developmen
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    User Protocols

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

    Vector Map

    Title
    TB074VM pET-28a-c(+) Vector Map

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