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69992 OrientExpress™ Random Primer cDNA Synthesis Kit

69992
  
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      Overview

      Replacement Information
      Description
      OverviewThe OrientExpress™ cDNA Synthesis and Cloning Systems are complete sets of reagents designed for rapid, efficient construction of cDNA libraries having inserts in a defined orientation. Six systems are available based on the following vectors: a bacteriophage lambda insertion vector, λSCREEN-1, and two bacteriophage T7 vectors, T7Select1-1 and T7Select10-3. Each vector is available as a kit designed for either random or oligo(dT) priming. The OrientExpress Random Primer System is based on a patented, directional random primer strategy. The OrientExpress Oligo(dT) System uses a modification of conventional oligo(dT) priming to achieve orientation-specific cloning between EcoR I and Hind III sites. Starting with high-quality poly(A)+ RNA, up to five cDNA libraries can be constructed with either system.

      The strategies for directional random primed and oligo(dT) primed cDNA synthesis are shown below. Both priming methods utilize special EcoR I/Hind III Linkers that generate a Hind III site only when ligated to sequences having AA at the 3′-end. The proper 3′-end is specified by the Hind III Random primers or by the Oligo(dT) primer used for first strand synthesis. Digestion with EcoR I and Hind III produces cDNA with an EcoR I site on one end and a Hind III site on the other, corresponding to the 5′- and 3′-ends of the mRNA, respectively. Ligation into EcoR I/Hind III vector arms produces inserts having a "sense" orientation relative to upstream expression signals.

      Both methods produce large libraries; however, random primed libraries provide more even sequence representation and offer the ability to modify average insert size by adjusting the ratio of primers to mRNA in the first strand reaction. This feature is useful for creating libraries of protein functional domains for screening by ligand binding assays. It should be noted that, unlike oligo(dT), random primers will efficiently prime any RNA present in the sample. Therefore, we recommend using highly purified poly(A)+ RNA for random primed library construction to minimize the occurrence of rRNA and other "junk" sequences in the library. The Straight A's™ mRNA Isolation System is designed for the preparation of poly(A)+ RNA suitable for random priming.





      For rapid, size fractionation of DNA and removal of small molecules (<300bp) from DNA solutions, please consider the Mini Column Fractionation Kit (Cat. No. 69995).
      Catalogue Number69992
      Brand Family Novagen®
      References
      Product Information
      Components
      DeclarationThis product is covered by U.S. Patent 5,629,179 owned by EMD Chemicals Inc. or its Affiliates
      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 Blue Ice Only
      Toxicity Multiple Toxicity Values, refer to MSDS
      Storage Multiple storage requirements
      Avoid freeze/thaw Avoid freeze/thaw
      Do not freeze Ok to freeze
      Packaging Information
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      Supplemental Information
      Specifications
      Global Trade Item Number
      Catalogue Number GTIN
      69992 0

      Documentation

      Required Licenses

      Title
      PRODUCTO REGULADO POR LA SECRETARÍA DE SALUD

      OrientExpress™ Random Primer cDNA Synthesis Kit Certificates of Analysis

      TitleLot Number
      69992

      Citations

      Title
    • Xinchun Shen, et al. (2005) Scanning the human proteome for calmodulin-binding proteins. Proceedings of the National Academy of Sciences (USA) 102, 5969-5974.
    • Paul Whitley, et al. (2003) Identification of mammalian Vps24p as an effector of phosphatidylinositol 3,5-bisphosphate-dependent endosome compartmentalization. Journal of Biological Chemistry 278, 38786-38795.
    • Valerie A Fadok, et al. (2000) A receptor for phosphatidylserine-specific clearance of apoptotic cells. 405, 85-90.
    • Huiming Guo, et al. (2000) EMMPRIN (CD147), an inducer of matrix metalloproteinase synthesis, also binds interstitial collagenase to the tumor cell surface. Cancer Research 60, 888-891.
    • M. Yamamoto, Y. Kominato and F. Yamamoto. (1999) Phage display cDNA cloning of protein with carbohydrate affinity. Biochemical and Biophysical Research Communications 255, 194-199.
    • User Protocols

      Title
      TB178 T7Select® System Manual
      TB247 OrientExpress™ cDNA Manual

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      Categories

      Life Science Research > Genomic Analysis > DNA Preparation & Cloning > Cloning > Cloning Kits
      Life Science Research > Genomic Analysis > Transfection and Protein Expression > Bacterial Expression > Bacterial Expression Vectors