ライフサイエンスコーパス: cloning vector

1 The vehicle can also be adapted as an ORF-cloning vector.

2 olated the corresponding genomic DNA in a P1 cloning vector.

3 omic library that had been generated in a P1 cloning vector.

4 that focus on the modular nature of plasmid cloning vectors.

5 r chromosome stability and as large-fragment cloning vectors.

6 es make it compatible with most conventional cloning vectors.

7 Escherichia coli DH10B using the pBeloBAC11 cloning vector; 678 individual insert termini of 339 BAC

8 pared with control strains carrying only the cloning vector, adsorbed out antibodies to PS/A from imm

9 The transcripts were cloned in a TA cloning vector and sequenced.

10 We create cloning vector and target molecules flanked with compati

11 in assembly and is employed extensively as a cloning vector and vehicle for peptide display.

12 We have constructed general cloning vectors and demonstrated single-column purificat

13 have many advantages over other large-insert cloning vectors and have been used for a variety of gene

14 protein assembly and are used extensively as cloning vectors and vehicles for peptide display.

15 mutants, for complementation with different cloning vectors, and for methods such as negative select

16 These cloning vectors are derived from a small cryptic plasmid

17 nalyzed and compared in a series of promoter cloning vectors by measuring the amount of lacZ mRNA by

18 p vectors, which contain features for direct cloning vector-cell fusion transcripts and for post-entr

19 transformants had human DNA YACs when a TAR cloning vector contained Alu repeats.

20 iae between genomic DNA and a linearized TAR cloning vector containing targeting sequences homologous

21 TAR cloning vectors containing the F-factor origin of replic

22 ort the creation of a new positive-selection cloning vector dubbed pKILLIN, which overcomes all of th

23 pGK12 or its derivative pED1 to develop new cloning vectors for B. burgdorferi with the rationale th

24 the future expansion of recombination-based cloning vectors for plant research.

25 ion, and the development of extrachromosomal cloning vectors, genetic analysis of Borrelia burgdorfer

26 A series of versatile cloning vectors has been constructed that facilitate the

27 from the FokI restriction endonuclease in a cloning vector of choice.

28 sign of probes that bind specifically to the cloning vector of DNA recombinants to facilitate physica

29 machines frequently contain fragments of the cloning vector on their ends.

30 mmunized with Salmonella containing only the cloning vector or PBS were not.

31 The results with a circular TAR cloning vector or two vectors differed from results with

32 Specifically, the P1 cloning vector pAd10sacBII was modified by the insertion

33 The bacterial cloning vector, pGreenscript A, derived from the mutated

34 We developed a purification-free cloning vector pGT3 with a bright green fluorescent prot

35 e that H1-expressed hairpins, as well as the cloning vector, reduce the plating efficiency of HeLa ce

36 o rearrange upon integration, or because the cloning vectors remain attached to the globin inserts.

37 essment of promoter activities with promoter cloning vectors requires careful analysis and interpreta

38 facilitated by the development of versatile cloning vectors, robust gene transfer systems and transp

39 This new cloning vector should improve the efficiency of performi

40 ibed here delineate the most frequently used cloning vectors such as BACs, P1s, PACs and YACs.

41 -donor commonly employed in Escherichia coli cloning vectors, such as pUC19, did not restore beta-Gal

42 at low temperatures, we constructed a set of cloning vectors suitable for rapidly positioning PCR pro

43 therefore developed a novel Escherichia coli cloning vector (termed 'pJAZZ' vector) that is maintaine

44 address this question, we developed a lambda cloning vector that allowed us to clone fragments spanni

45 ies, we constructed a new TAR-BRV- tTA(VP64) cloning vector that allows a selective isolation of a ge

46 Exogenous DNA is introduced on a cloning vector that contains an FRT, selectable markers,

47 rted into a specialized bacteriophage lambda cloning vector that must acquire a functional lysozyme g

48 We have developed a Gram-positive cloning vector that utilizes the interruption of an alka

49 pment and analysis of broad-host-range (BHR) cloning vectors that carry the araC-PBAD controlled expr

50 hat can be applied to cDNA clones with large cloning vectors, thereby overcoming a potential limitati

51 tion and the DNA-carrying capacity of modern cloning vectors, thus facilitating merger of genetic and

52 The ORFs were captured in a recombinational cloning vector to facilitate high-throughput transfer of

53 ss how to design appropriate C. elegans BiFC cloning vectors to enable visualization of protein inter

54 se of a complete lack of selectable markers, cloning vectors, transposons, and convenient methods of

55 ctor-derived bacterial artificial chromosome cloning vector used in Escherichia coli, with the additi

56 We released HBV genome from the cloning vector using BspQI, an inexpensive isoschizomer

57 The filamentous phages are important as cloning vectors, vehicles for peptide display, and subst

58 A TAR cloning vector was constructed that, when linearized, co

59 A specialized cloning vector was developed for capture and analysis of

60 A family of specific cloning vectors was constructed to express in the cyanob

61 A series of recombination cloning vectors was generated to accelerate the expressi

62 ing an ampicillin resistance gene (bla) from cloning vectors was not detected in either the wastewate

63 d-specific RNA interference gene-suppression cloning vectors were also constructed for silencing of e

64 d a pair of differentially marked linear TAR cloning vectors where one contained a small fragment of

65 A cDNA cloning vector which carries a modified invertase gene l

66 actinomycetes; (2) self-replicating plasmid-cloning vectors, which generally inhibit secondary-metab