ライフサイエンスコーパス: cloned DNA

1 8 kb, and is expected to contain ~1.54 GB of cloned DNA.

2 ble array construction from small amounts of cloned DNA.

3 nce of large arrays of repeated sequences in cloned DNA.

4 by contig construction of maps derived from cloned DNA.

5 herichia coli to produce large quantities of cloned DNA.

6 e levels of both the recombinational map and cloned DNA.

7 ctor, we have mapped wun to within 100 kb of cloned DNA.

8 WMHBV replication following transfection of cloned DNA.

9 c regulatory aspects of mRNA biogenesis from cloned DNAs.

10 spsK gene and the pssDE genes by segments of cloned DNA and by the SpsK-dependent incorporation of ra

11 RT dimerization, we introduced changes into cloned DNA and tested the mutant subunits for their capa

12 al for the amplification and manipulation of cloned DNA and the production of recombinant proteins.

13 Expression of several of the ORFs from cloned DNA appears to be toxic to the host bacteria.

14 olecules are produced from either genomic or cloned DNA by PCR using labeled primers and are tethered

15 ong-range restriction mapping of genomic and cloned DNA by pulsed-field gel electrophoresis.

16 Mutations in ine were localized on cloned DNA by restriction mapping and restriction fragme

17 nsertion site was cloned from RS218, and the cloned DNA complemented the TnphoA mutant in invasion of

18 ymorphism (RFLP) analysis confirmed that the cloned DNA contained the arg-14 gene.

19 ish overlaps between contiguous stretches of cloned DNA derived from genomic regions.

20 munoglobulin heavy chain expression, we have cloned DNA downstream from the two human Calpha genes, c

21 Using a PCR approach, we have cloned DNA encoding a catalytic subunit isoform (SnRK1-a

22 ties of human MT4-MMP (i.e. MMP-17), we have cloned DNA encoding its catalytic domain (CD) from a bre

23 Cells heterologously expressing the cloned DNA encoding the GABA(B)R1 protein exhibit high-a

24 RNA polymerase III of purified, circularized cloned DNAs encoding genes for 5S rRNA was detectable lo

25 calization of selectable marker genes in the cloned DNA ensures the integrity of the genomic fragment

26 Evidence that the cloned DNA faithfully represents the source genomic DNA

27 a suppressor gene, and provide the necessary cloned DNA for more detailed physical mapping and gene i

28 e candidate genes, and provide the necessary cloned DNA for the positional cloning of the RP10 gene.

29 rified Escherichia coli RNA polymerase and a cloned DNA fragment carrying the entire melibiose operon

30 A 13-kb cloned DNA fragment containing the P. putida crc gene re

31 DNA sequencing of the cloned DNA fragment suggested that a previously characte

32 rtial open reading frame were located on the cloned DNA fragment.

33 Cloned DNA fragments containing the parental dapB gene r

34 lly bind a well-characterized yeast SAR, and cloned DNA fragments derived from the 3'-flanking region

35 Sequence analysis of cloned DNA fragments expanded by Taq polymerase indicate

36 ential hybridization of arrayed libraries of cloned DNA fragments was developed.

37 The cloned DNA fragments were used as probes to perform Nort

38 NA complementary to mRNA populations (cDNA), cloned DNA fragments, and even PCR products.

39 ymphoblast cell cultures (CHR and 9947A) and cloned DNA from the CHR HV1 region, which contains a C s

40 hen a replicative plasmid carrying a USS and cloned DNA from the chromosome of A. actinomycetemcomita

41 Cloned DNAs from the characteristic bulbous structure at

42 Characterization of the cloned DNA in the recombinant YAC demonstrated that it w

43 om coverage of the whole genome using 200 kb cloned DNA inserts to detailed analysis using PCR produc

44 The introduction of cloned DNA into mammalian cells allows functional testin

45 cumvent host restriction, and integration of cloned DNA into neutral genomic sites prevents product i

46 PCR (MSP) and by bisulfite DNA sequencing of cloned DNA of PCR amplicons.

47 The distribution of cloned DNAs on chromosome 16 was determined by fluoresce

48 Of the five cloned DNA polymerases, the Thermococcus sp. 9 degrees N

49 Cloned DNA probes containing the lactose operon (lac) an

50 an E. coli entF mutant complemented with the cloned DNA regained the ability to synthesize enterobact

51 f human chromosome 17p, and will provide the cloned DNA required for ascertaining the nucleotide sequ

52 Sequence analysis of the cloned DNA revealed an open reading frame of 290 codons

53 recombinase of yeast to introduce exogenous cloned DNA reversibly at defined locations in the Escher

54 between the targets, or by the length of the cloned DNA segments.

55 one-hybrid system, where the activation of a cloned DNA sequence from a library of random DNA-binding

56 Analysis of the cloned DNA sequence revealed a 438-bp open reading frame

57 is and high-resolution functional mapping of cloned DNA sequences.

58 e (TIL), which can minimize manipulations in cloned DNA sequencing and in bioinformatics.

59 s identified numerous instances in which the cloned DNAs shared significant sequence similarities to

60 Clustered in the center of the cloned DNA stretch are six genes responsible for the con

61 iments comparing genomic DNA to unmethylated cloned DNA suggested that the melting variants were most

62 d protein NAP-1 in assembling chromatin onto cloned DNA templates in cooperation with the remodeling

63 be important to determine whether mutants of cloned DNAs that produce abnormal amounts of stable mRNA

64 Here we use recently cloned DNA to demonstrate that segments located sequenti

65 We have cloned DNA upstream of the omega 4403 insertion site, lo

66 or, fepA, and the utilization gene, fes, the cloned DNA was examined for the ability to restore sider

67 was cloned and sequenced, and 3.5 kb of the cloned DNA was targeted for PCR amplification.