Rat Liver QUICK-Clone cDNA

Rat Liver QUICK-Clone cDNA

Brand: Takara Bio.
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Rat Liver QUICK-Clone cDNA
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Rat Liver QUICK-Clone™ cDNA
SKU: 637313
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Rat Liver QUICK-Clone cDNA
Rat Liver QUICK-Clone cDNA

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A high-quality cDNA template is necessary to obtain good results from PCR amplification. QUICK-Clone cDNA is premade double-stranded cDNA from which you can amplify sequences of interest using gene-specific primers, and is ideal for amplifying previously isolated, structurally related, or cross-species cDNAs. Synthesized from premium, high-quality poly A+ RNA from various rat tissues using an oligo(dT) primer, QUICK-Clone cDNA is purified to remove residual RNA and size-selected to eliminate cDNA fragments smaller than 400 bp.  QUICK-Clone cDNA allows you to amplify cDNAs of interest while avoiding traditional library construction and screening steps, and can also be used to generate hybridization probes using gene-specific or degenerate primers (Parmentier et al. 1989; Wilks et al. 1989; Vallins et al. 1990; Lee et al. 1988; Schuchman, Jackson, and Desnick 1990).

Overview

  • Highly purified double-stranded cDNA
  • Clone genes directly by PCR, rather than library screening
  • Prepared from high-quality human tissues and cell lines
  • Ideal for amplifying previously isolated, structurally related, or cross-species cDNAs

Applications

  • Clone cDNAs without library screening
  • Generate hybridization probes using gene-specific or degenerate primers
  • Ideal for amplifying previously isolated, structurally related, or cross-species cDNAs

Lee, C. C. et al. Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase. Science 239, 1288–91 (1988).

Parmentier, M. et al. Molecular cloning of the thyrotropin receptor. Science 246, 1620–2 (1989).

Schuchman, E. H., Jackson, C. E. & Desnick, R. J. Human arylsulfatase B: MOPAC cloning, nucleotide sequence of a full-length cDNA, and regions of amino acid identity with arylsulfatases A and C. Genomics 6, 149–58 (1990).

Vallins, W. J. et al. Molecular cloning of human cardiac troponin I using polymerase chain reaction. FEBS Lett. 270, 57–61 (1990).

Wilks, A. F., Kurban, R. R., Hovens, C. M. & Ralph, S. J. The application of the polymerase chain reaction to cloning members of the protein tyrosine kinase family. Gene 85, 67–74 (1989).    

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A high-quality cDNA template is necessary to obtain good results from PCR amplification. QUICK-Clone cDNA is premade double-stranded cDNA from which you can amplify sequences of interest using gene-specific primers, and is ideal for amplifying previously isolated, structurally related, or cross-species cDNAs. Synthesized from premium, high-quality poly A+ RNA from various rat tissues using an oligo(dT) primer, QUICK-Clone cDNA is purified to remove residual RNA and size-selected to eliminate cDNA fragments smaller than 400 bp.  QUICK-Clone cDNA allows you to amplify cDNAs of interest while avoiding traditional library construction and screening steps, and can also be used to generate hybridization probes using gene-specific or degenerate primers (Parmentier et al. 1989; Wilks et al. 1989; Vallins et al. 1990; Lee et al. 1988; Schuchman, Jackson, and Desnick 1990).

Overview

  • Highly purified double-stranded cDNA
  • Clone genes directly by PCR, rather than library screening
  • Prepared from high-quality human tissues and cell lines
  • Ideal for amplifying previously isolated, structurally related, or cross-species cDNAs

Applications

  • Clone cDNAs without library screening
  • Generate hybridization probes using gene-specific or degenerate primers
  • Ideal for amplifying previously isolated, structurally related, or cross-species cDNAs

Lee, C. C. et al. Generation of cDNA probes directed by amino acid sequence: cloning of urate oxidase. Science 239, 1288–91 (1988).

Parmentier, M. et al. Molecular cloning of the thyrotropin receptor. Science 246, 1620–2 (1989).

Schuchman, E. H., Jackson, C. E. & Desnick, R. J. Human arylsulfatase B: MOPAC cloning, nucleotide sequence of a full-length cDNA, and regions of amino acid identity with arylsulfatases A and C. Genomics 6, 149–58 (1990).

Vallins, W. J. et al. Molecular cloning of human cardiac troponin I using polymerase chain reaction. FEBS Lett. 270, 57–61 (1990).

Wilks, A. F., Kurban, R. R., Hovens, C. M. & Ralph, S. J. The application of the polymerase chain reaction to cloning members of the protein tyrosine kinase family. Gene 85, 67–74 (1989).    

Write Your Own Review
You're reviewing:Rat Liver QUICK-Clone cDNA
Your Rating