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using Primer3 according to the reference sequences in the NCBI Gene database(passive) were designedThe primers ( Table 2 ) for polymerase chain reaction ( PCR
Primer 3 software ( http://primer3.ut.ee/ ) and(passive) were designed byThe primers used for polymerase chain reaction ( PCR
The Primer - BLAST tool uses Primer3to designPCR primers to a sequence template
using the published sequence of the human(passive) were designedoligonucleotide primers for polymerase chain reaction ( PCR
using Primer3 software(passive) were designedPrimers for polymerase chain reaction ( PCR
PCR ) amplification(passive) were designedSpecific primers for polymerase chain reaction
the universal primers(passive) were designedResults For the primer - template mismatch PCR
the software(passive) were designed byMethods Polymerase chain reaction primers
Assay Designer 3.1(passive) were designed byThe primers for polymerase chain reaction ( PCR
However , this approach yields information only for specifically targeted CRISPRs and for organisms with sufficient representation in public databasesto designreliable polymerase chain reaction ( PCR ) primers
for the detection and cloning of the neuraminidase genes that are nanA(passive) are designedThree primer sets for polymerase chain reaction ( PCR
PCR(passive) were designedOligonucleotide primers for polymerase chain reaction
Competitors ... many other software programsdesignprimers for the PCR reaction
A toolto designtarget - specific primers for polymerase chain reaction
to amplify and sequence novel Circovirus DNA from affected feathers(passive) were designedDegenerate polymerase chain reaction primers
to amplify all coding exons and exon / intron boundaries of the COL2A1 gene(passive) were designedPolymerase chain reaction primers
to start from intronic sequences(passive) were designedAll the primers for polymerase chain reaction
to amplify(passive) were designedPolymerase chain reaction primers
amino acidsto designdegenerate primers for polymerase chain reaction
based on conserved motifs within the serine protease and RNA helicase domains encoded by the NS 3 genes of dengue and other flaviviruses(passive) were designedConsensus primers for the polymerase chain reaction
Similarly ,when designingprimers for polymerase chain reaction
to distinguish the TP53 retrogenes from the ancestral sequence and splice variants(passive) were designedPolymerase chain reaction primers
the coverage of the genome ... a single experimentwhere designedprimer in the PCR reaction
to discriminate between mutant and wild - type alleles of glucocerebrosidase and to allow separation from products of the related pseudogene(passive) were designedPrimers for the polymerase chain reaction
The slowly - evolving regions can be usedto designbroad - spectrum primer pairs for polymerase chain reaction
The idea to study and apply molecular genetics in Vietnam appeared in our mind since 1988 ,originatingfrom Kary Mulis 's discovery on Polymerase Chain Reaction ( PCR
Kary Mullis(passive) was discovered byPOLYMERASE CHAIN REACTION The polymerase chain reaction ( PCR
Primer - BLAST(passive) was designedPrimer - BLAST
Primers(passive) were designedPrimers
in the isolation of a human cDNAresultedin the isolation of a human cDNA
in the amplification of target DNAwould resultin the amplification of target DNA
based on the known cDNA sequenceare designedbased on the known cDNA sequence
in the isolation of a human cDNA for a previously unidentified DNA polymerase ( designated DNA polymerase beta2 ) that is closely related to DNA polymerase beta ( Pol betaresultedin the isolation of a human cDNA for a previously unidentified DNA polymerase ( designated DNA polymerase beta2 ) that is closely related to DNA polymerase beta ( Pol beta
to be specific fordesignedto be specific for
displacement of the probe from the template and probe degradationcausesdisplacement of the probe from the template and probe degradation
for mutation screeningdesignedfor mutation screening
with knowledge of the human HK1 cDNA sequencedesignedwith knowledge of the human HK1 cDNA sequence
for early detection of TGIVdesignedfor early detection of TGIV
duplicated sequence(passive) caused byduplicated sequence
from this sequencedesignedfrom this sequence
referring to the NTF4 gene sequence from the Ensembl databasedesignedreferring to the NTF4 gene sequence from the Ensembl database
PCR bias(passive) caused byPCR bias
for Globicephaladesignedfor Globicephala
forth in SEQ IDsetforth in SEQ ID
the bias(passive) caused bythe bias
A fluorescent DNA probe ( LEIS.P1 ) specific for a conserved region of the small - subunit ribosomal RNA gene of Leishmania and a pair of flanking primers ( LEIS.U1 and LEIS.L1(passive) were designedA fluorescent DNA probe ( LEIS.P1 ) specific for a conserved region of the small - subunit ribosomal RNA gene of Leishmania and a pair of flanking primers ( LEIS.U1 and LEIS.L1
allelic dropoutcauseallelic dropout
in poor amplificationresultsin poor amplification
The unexpected ease of extending the C.T mismatch(passive) to have been caused byThe unexpected ease of extending the C.T mismatch
for the simultaneous detection of four viruses involved in reproductive and respiratory failure in pigswas designedfor the simultaneous detection of four viruses involved in reproductive and respiratory failure in pigs
the pair of PCR primers to amplify the segment of interest in the input DNA sequencedesignsthe pair of PCR primers to amplify the segment of interest in the input DNA sequence