ライフサイエンスコーパス: forward primer

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1 approach is combined with a mutant-specific forward primer.

2 Then, a DNA polymerase extends the bound forward primer along the C-probe and continuously displa

3 s then performed using a transcript-specific forward primer and a reverse primer that is identical to

4 electrophoresis sequencing with the M13(-21)forward primer and by generating and analyzing a set of

5 The forward primer and fusion probe were redesigned from the

6 imers (i.e. a combination of gene A specific forward primer and gene B specific reverse primer, etc.)

7 By amplification with MLL exon 5 forward primer and reverse primers in MSF, the appropria

8 In the first reaction, the forwarding primer and an additional 20-nt-long sequence

9 n immediately following the 3' end of the E2 forward primer binding site was found to be responsible

10 tubes, the first for yeasts, containing the forward primer CandUn (5'CATGCCTGTTTGAGCGTC) and the rev

11 In the second reaction, a forwarding primer containing as 5' overhang sequence the

12 Two distinct forward primers, each of which contains a 3'-terminal ba

13 second for filamentous fungi, containing the forward primer FilamUn1 (5'TGCCTGTCCGAGCGTCAT) and FungU

14 In both cases, forward primer for Francisella tularensis holarctica gen

15 Reverse transcriptase PCR using a forward primer from ASPL and a TFE3 exon 4 reverse prime

16 ctyls, swine and sheep, was identified using forward primers from the psiJalpha region, and reverse p

17 er (Hbr) and the Helicobacter genus-specific forward primer (H276f) amplified H. bilis DNA but not DN

18 Each of the forward primers has a common 22-base sequence at its 5'

19 Our method uses two species-specific forward primers in combination with a single reverse pri

20 The forward primer is attached to the ECP.

21 was amplified in the envelope gene with the forward primer labeled in the PCR.

22 on and solid-phase elongation of immobilised forward primers on specific rings, at a constant tempera

23 ted within the annealing site of the exon 13 forward primer, prevented amplification of exon 13 in th

24 hod, microbeads functionalized with multiple forward primers targeting specific genes from different

25 assay uses TaqMan technology, employing two forward primers, three reverse primers, and four fluorop

26 An amino-modified forward primer was covalently labeled onto the MPNP surf

27 Forward primers were designed that would specifically am

28 s confirmed by the fact that (i) none of our forward primers were homologous to the 16S rRNA genes of

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