ライフサイエンスコーパス: terminator sequence

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1 poly(A) (pA) signal and, often, a downstream terminator sequence.

2 monly used Hsp70A-RBCS2 (AR) hybrid promoter/terminator sequences.

3 ontext of both natural and artificial Pol II terminator sequences.

4 ired for the removal of the 3' Rho-dependent terminator sequences.

5 en the RNA polymerase I (pol I) promoter and terminator sequences.

6 e a reduced frequency of termination at T(5) terminator sequences.

7 n by simply attaching mammalian promoter and terminator sequences.

8 ic Tet repressor and elongation halted by T7 terminator sequences.

9 flanked by Aspergillus nidulans promoter and terminator sequences.

10 iboswitch by extending alignments to include terminator sequences.

11 f the sagA promoter and (ii) downstream of a terminator sequence after sagI did not affect SLS produc

12 Sanger dideoxy terminator sequencing allows for rapid development and i

13 tion mechanisms and the relationship between terminator sequence and steps in the termination mechani

14 Termination begins in the wild-type trp t' terminator sequence approximately 97 bps downstream of t

15 transcription antiterminator and attenuation terminator sequences are absent from their pyr 5' leader

16 confirm that complementary direct repeat and terminator sequences are involved in the formation of th

17 In yeast, terminator sequences are present in rDNA non-transcribed

18 osition near the 5'-end, and a rho-dependent terminator sequence at the 3'-end to which complementary

19 ll 135 reported terminators and 940 putative terminator sequences beginning no more than 60 nt away f

20 A rho-independent terminator sequence between sagA and sagB appears to reg

21 e terminator, tR1, containing inserts of non-terminator sequences between its rut and tsp regions wer

22 A DNA replication terminator sequence blocks an approaching replication fo

23 mer extension DNA fragments generated in dye-terminator sequencing cause background noise in fluoresc

24 B1-Alu genes that differ only in terminator sequence context direct differential RNA 3' e

25 We used these data to determine how the terminator sequence contributes to its strength.

26 o consensus sequence dideoxynucleotide chain terminator sequencing for detection of 91 drug resistanc

27 rbonate (PC) for purification of dye-labeled terminator sequencing fragments using solid-phase revers

28 SPRI cleanup of dye-terminator sequencing fragments using the photoactivated

29 By virtue of weak terminator sequences in some T-DNA constructs, transcrip

30 resulted in the incorporation of the t(Mx8) terminator sequence, in addition to a short sequence of

31 ion extension past a potential transcription terminator sequence IRS1.

32 ganese salt to the PE Applied Biosystems dye-terminator sequencing kits overcomes these limitations f

33 oligos have been synthesized for use in dye terminator sequencing reactions, polymerase chain reacti

34 from a classical pol III gene (tRNAiMet) in terminator sequence requirements.

35 ene under the control of the U1 promoter and terminator sequences resulted in the highest levels of c

36 pothesize that the integration of the t(Mx8) terminator sequence results in reduced levels of mature

37 t of the HasS variations were located in the terminator sequences, suggesting that this region is und

38 , and both provide more even peak heights in terminator sequencing than the dye-terminators consistin

39 th the putative promoter and rho-independant terminator sequences that flank these two genes.

40 mismatch repair detection (MRD) with dideoxy terminator sequencing to detect SNPs in pooled DNA sampl

41 Modified dye terminator sequencing was generally useful for the seque

42 tion followed by Illumina NextSeq reversible terminator sequencing with DNA selection by amplificatio

43 istently gave read lengths comparable to dye-terminator sequencing with longer primers.

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