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Titlebook: Methods in DNA Amplification; Arndt Rolfs,Ines Weber-Rolfs,Ulrich Finckh Book 1994 Springer Science+Business Media New York 1994 Hepatitis

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Impact of PCR on the Pathologist’s Worldrld that perform PCR, many in a more or less routine manner to detect a variety of conditions. They can be divided into 3 general categories: I) Low copy number of foreign nucleic acid. These are generally infectious diseases. Two examples are Hepatitis C Virus (HCV) and Cytomegalovirus (CMV). II) S
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Polymorphic Keratins as Detected by PCR and SSCPmolecular basis of the differences among the alleles of these genes, we have analyzed their N- and C-terminal domains following amplification of genomic DNA by the polymerase chain reaction. Whereas the Kl and the K10 alleles differ in size of their carboxyl-terminal V2 subdomains, the alleles of th
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Use of Chelex 100TM in the Extraction of Viruses from Diverse Cell-Free Clinical Samples for PCRaddition of a number of reagents. This may cause loss of valuable target material and cross-contamination, and increase the opportunity for errors. It may also reduce the number of samples that might conveniently be handled at one time.
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Resolution of a Secondary Structure in an Unknown mRNA 5’ Ende full-length 5’end of the sense strand. The RACE (rapid amplification of cDNA ends) PCR technique first described by Frohman et al (1988) has proven to be a versatile and fast method for obtaining the complete 5’end of cDNAs.
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