Examples of using PCR amplification in English and their translations into Spanish
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gain of a cysteine residue in the extracellular regions of NOTCH3 gene associated with CADASIL, by PCR amplification and subsequent sequencing of exons 3,
It is suggested to start the study by PCR amplification followed by sequencing CDKN2A if prior family history of melanomas and, if found necessary,
RT of the extracted RNA,(iii) PCR amplification of the RT product and(iv)
bubaline herpesvirus 1), improved methods are available using monoclonal antibodies(Keuser et al., 2004) or PCR amplification and sequencing Ros et al., 1999.
by commercial kits that are widely available;(b) standard PCR amplification using oligonucleotide sequences(primers) selected from the small-subunit rRNA gene(Mathis& Deplazes,
Duplicate PCR amplifications should be carried out for each DNA preparation(six amplifications in total)
MRPY gene detection by PCR amplification.
PCR amplification of the RT product is performed by a different procedure.
The samples were screened by PCR amplification of the meq full-length gene.
COL genes were obtained by PCR amplification.
Kb PCR amplification with 20 pg of template or less.
Molecular Detection by genomic PCR amplification followed by sequencing if desired to know the species.
in IVAMI perform detection HLA-B* 5701, using the complete PCR amplification and subsequent sequencing.
ready-to-load reaction cocktail for PCR amplification of up to 4 kb.
Molecular detection of each species/ strains of Avipoxvirus, by genomic PCR amplification and their typing by nucleic acid sequencing.
diarrhea syndrome, by PCR amplification of the corresponding genes.
For multiplex PCR amplification of partial 16S rRNA(=SSU rRNA) gene fragments, the following primer combination can be used.
If negative result is the possibility of carrying out the sequence analysis CDKN2A complete by PCR amplification followed by direct sequencing.
PCR amplification, either for real-time PCR
in IVAMI perform detection of mutations associated with Kearns-Sayre syndrome, by PCR amplification of complete deletions in mitochondrial DNA.