戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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      The range of available copy numbers for cloning vectors is largely restricted to the handful of
28  from the FokI restriction endonuclease in a cloning vector of choice.
29 sign of probes that bind specifically to the cloning vector of DNA recombinants to facilitate physica
30 machines frequently contain fragments of the cloning vector on their ends.
31 mmunized with Salmonella containing only the cloning vector or PBS were not.
32              The results with a circular TAR cloning vector or two vectors differed from results with
33                         Specifically, the P1 cloning vector pAd10sacBII was modified by the insertion
34                                The bacterial cloning vector, pGreenscript A, derived from the mutated
35             We developed a purification-free cloning vector pGT3 with a bright green fluorescent prot
36 e that H1-expressed hairpins, as well as the cloning vector, reduce the plating efficiency of HeLa ce
37 o rearrange upon integration, or because the cloning vectors remain attached to the globin inserts.
38 essment of promoter activities with promoter cloning vectors requires careful analysis and interpreta
39  facilitated by the development of versatile cloning vectors, robust gene transfer systems and transp
40                                     This new cloning vector should improve the efficiency of performi
41 ibed here delineate the most frequently used cloning vectors such as BACs, P1s, PACs and YACs.
42 -donor commonly employed in Escherichia coli cloning vectors, such as pUC19, did not restore beta-Gal
43 at low temperatures, we constructed a set of cloning vectors suitable for rapidly positioning PCR pro
44 therefore developed a novel Escherichia coli cloning vector (termed 'pJAZZ' vector) that is maintaine
45 address this question, we developed a lambda cloning vector that allowed us to clone fragments spanni
46 ies, we constructed a new TAR-BRV- tTA(VP64) cloning vector that allows a selective isolation of a ge
47             Exogenous DNA is introduced on a cloning vector that contains an FRT, selectable markers,
48 rted into a specialized bacteriophage lambda cloning vector that must acquire a functional lysozyme g
49            We have developed a Gram-positive cloning vector that utilizes the interruption of an alka
50 pment and analysis of broad-host-range (BHR) cloning vectors that carry the araC-PBAD controlled expr
51 hat can be applied to cDNA clones with large cloning vectors, thereby overcoming a potential limitati
52 tion and the DNA-carrying capacity of modern cloning vectors, thus facilitating merger of genetic and
53  The ORFs were captured in a recombinational cloning vector to facilitate high-throughput transfer of
54 ss how to design appropriate C. elegans BiFC cloning vectors to enable visualization of protein inter
55 se of a complete lack of selectable markers, cloning vectors, transposons, and convenient methods of
56 ctor-derived bacterial artificial chromosome cloning vector used in Escherichia coli, with the additi
57              We released HBV genome from the cloning vector using BspQI, an inexpensive isoschizomer
58      The filamentous phages are important as cloning vectors, vehicles for peptide display, and subst
59                                        A TAR cloning vector was constructed that, when linearized, co
60                                A specialized cloning vector was developed for capture and analysis of
61                         A family of specific cloning vectors was constructed to express in the cyanob
62                    A series of recombination cloning vectors was generated to accelerate the expressi
63 ing an ampicillin resistance gene (bla) from cloning vectors was not detected in either the wastewate
64 d-specific RNA interference gene-suppression cloning vectors were also constructed for silencing of e
65 d a pair of differentially marked linear TAR cloning vectors where one contained a small fragment of
66                                       A cDNA cloning vector which carries a modified invertase gene l
67  actinomycetes; (2) self-replicating plasmid-cloning vectors, which generally inhibit secondary-metab