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Titlebook: cDNA Library Protocols; Ian G. Cowell,Caroline A. Austin Book 1997 Springer Science+Business Media New York 1997

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Topological and Algebraic Considerationsdouble-stranded DNA probe containing the sequence recognized by the factor in question. Recombinants expressing a protein capable of binding the probe sequence in the presence of nonspecific competitor DNA are thus identified and can be isolated.
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Book 1997iptase) to convert poly A* mRNA into double-stranded cDNA suitable for insertion into prokaryotic vectors. Since then cDNA technology has become a fundamental tool for the molecular biologist and at the same time some very significant advances have occurred in the methods for con- structing and scre
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Applications in Statistical ComputingA fragments, In this case, treatment of the mRNA with a denaturant, such as methyl-mercuric hydroxide, prior to synthesis may be necessary (.). Other potential difficulties include DNA molecules contaminating the mRNA sample. DNA can clone efficiently, and their introns can confuse results. RNase-free DNase treatment of the sample is recommended.
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Pascal Kerschke,Heike Trautmannnd, the intrinsic difficulty of multiple sequential enzymatic reactions required for cDNA cloning often leads to low yields and truncated clones (.). Finally, screening of a library with hybridization technique is time consuming.
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,cDNA Library Construction for the Lambda ZAP?-Based Vectors,A fragments, In this case, treatment of the mRNA with a denaturant, such as methyl-mercuric hydroxide, prior to synthesis may be necessary (.). Other potential difficulties include DNA molecules contaminating the mRNA sample. DNA can clone efficiently, and their introns can confuse results. RNase-free DNase treatment of the sample is recommended.
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