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1 urface, previously modified with a thiolated forward primer.
2  approach is combined with a mutant-specific forward primer.
3 ads were functionalized with biotin-modified forward primers.
4     Then, a DNA polymerase extends the bound forward primer along the C-probe and continuously displa
5                          Using a universal G forward primer and a newly designed reverse primer and T
6 s then performed using a transcript-specific forward primer and a reverse primer that is identical to
7  electrophoresis sequencing with the M13(-21)forward primer and by generating and analyzing a set of
8                                          The forward primer and fusion probe were redesigned from the
9 imers (i.e. a combination of gene A specific forward primer and gene B specific reverse primer, etc.)
10             By amplification with MLL exon 5 forward primer and reverse primers in MSF, the appropria
11                   In the first reaction, the forwarding primer and an additional 20-nt-long sequence
12 ndent qPCR due to sequence information for a forward primer, and for a reverse primer binding site, a
13 ases. Polymerase chain reaction (PCR) with a forward primer bearing a methanol-responsive polymer gen
14 n immediately following the 3' end of the E2 forward primer binding site was found to be responsible
15 ified point mutations C744T and A756G in the forward primer binding sites and G795A in the reverse pr
16  tubes, the first for yeasts, containing the forward primer CandUn (5'CATGCCTGTTTGAGCGTC) and the rev
17 lification of all target regions by up to 15 forward primers combined with 4 reverse primers.
18                    In the second reaction, a forwarding primer containing as 5' overhang sequence the
19                                 Two distinct forward primers, each of which contains a 3'-terminal ba
20 second for filamentous fungi, containing the forward primer FilamUn1 (5'TGCCTGTCCGAGCGTCAT) and FungU
21                               In both cases, forward primer for Francisella tularensis holarctica gen
22 nal oligonucleotide probes integrating (1) a forward primer for RPA, (2) a C9 spacer to stop polymera
23            Reverse transcriptase PCR using a forward primer from ASPL and a TFE3 exon 4 reverse prime
24              When the PCR is performed using forward primers from one chromosome and reverse primers
25 ctyls, swine and sheep, was identified using forward primers from the psiJalpha region, and reverse p
26 er (Hbr) and the Helicobacter genus-specific forward primer (H276f) amplified H. bilis DNA but not DN
27                                  Each of the forward primers has a common 22-base sequence at its 5'
28         Our method uses two species-specific forward primers in combination with a single reverse pri
29                                          The forward primer is attached to the ECP.
30  was amplified in the envelope gene with the forward primer labeled in the PCR.
31 on and solid-phase elongation of immobilised forward primers on specific rings, at a constant tempera
32 ted within the annealing site of the exon 13 forward primer, prevented amplification of exon 13 in th
33 hod, microbeads functionalized with multiple forward primers targeting specific genes from different
34  assay uses TaqMan technology, employing two forward primers, three reverse primers, and four fluorop
35                            An amino-modified forward primer was covalently labeled onto the MPNP surf
36 merase amplification using ferrocene labeled forward primers was employed to generate single stranded
37                                              Forward primers were designed that would specifically am
38 s confirmed by the fact that (i) none of our forward primers were homologous to the 16S rRNA genes of