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1 (LAC), through on-chip electrical sensing of bacterial lysate.
2 onstrated by the direct detection of rRNA in bacterial lysate.
3              We purified these proteins from bacterial lysates.
4 ot by normal HeLa cell lysates or irrelevant bacterial lysates.
5 both native and recombinant SodA activity in bacterial lysates.
6  as GST fusion proteins, to homogeneity from bacterial lysates.
7 was partially degraded during isolation from bacterial lysates.
8 plying a coumarin-based fluorogenic probe in bacterial lysates.
9 specific electrophoretic patterns from crude bacterial lysates.
10  to extract and focus 16S rRNA directly from bacterial lysate and used molecular beacons to achieve d
11 binds H-Ras.GTP in both pulldown assays from bacterial lysates and by coimmunoprecipitation from HEK2
12    All 13 fusion proteins were purified from bacterial lysates and used to test a panel of anti-HCV p
13 rformance was verified with model samples of bacterial lysates and with four real-matrix samples of k
14 ells are completely lyzed, and the resulting bacterial lysates are thoroughly mixed with the potassiu
15 sponding to whole Gram-negative bacteria and bacterial lysates, as demonstrated by NF-kappaB activati
16 revention of AD by oral supplementation of a bacterial lysate between week 5 and the end of month 7,
17            The protein was purified from the bacterial lysate by affinity chromatography using a biot
18  recapitulate the protection afforded by the bacterial lysate by stimulating the lung epithelium with
19 00Z protein was purified to homogeneity from bacterial lysates by a combination of hydrophobic column
20         The fusion protein was purified from bacterial lysates by affinity chromatography with an amy
21                            When exposed to a bacterial lysate containing estrogen receptor alpha liga
22 of month 7, infants were treated orally with bacterial lysate containing heat-killed gram-negative Es
23 ture of purified rabbit hsp90 and hsp70 with bacterial lysate containing human p60 results in spontan
24         The assay is sensitive enough to use bacterial lysates diluted 20 fold.
25  EIA with the current serodiagnostic test, a bacterial lysate EIA, revealed relatively good correlati
26  A new approach to the isolation of RNA from bacterial lysates employs selective precipitation by com
27           Expression of epitope-tagged S3 in bacterial lysates followed by photoaffinity labeling con
28 ous non-helicobacter bacteria, or with cecal bacterial lysate from uninfected mice.
29 noglobulin M (IgM) and IgA established using bacterial lysates from homologous (the infecting strain)
30 ght to evaluate the effect of orally applied bacterial lysate in infancy on the prevalence of atopic
31                                        Using bacterial lysates in dot blot analysis, a panel of sera
32 e use of prebiotics, probiotic bacteria, and bacterial lysates in early life, this review provides an
33  The effect of H. pylori recombinant urease, bacterial lysate, intact bacteria, and bacterial DNA on
34 ntify proteins and other molecules in single bacterial lysates is encouraging to use the new analysis
35 BFP is a different protein again, and in the bacterial lysate it occurs in multiple forms, ligated to
36                                   Feeding of bacterial lysate might have prevented the development of
37 tibody bound to recombinant SREHP present in bacterial lysates on immunoblots.
38  cell production of IFN-gamma in response to bacterial lysate or LPS was Ag independent and could be
39 te IFN-gamma in response to stimulation with bacterial lysate or LPS.
40 r treated animals with H. pylori components (bacterial lysate or the immunomodulator VacA) and subseq
41 dal lymph node CD4 + T cells stimulated with bacterial lysate-pulsed antigen-presenting cells.
42 stitution of germfree RAG-/- mice with cecal bacterial lysate-pulsed DCs, but not with IL-6-/- or Myd
43 nylation or by Western blotting of the whole bacterial lysate, suggesting that it is not expressed by
44 e induced therapeutically by inhalation of a bacterial lysate that protects mice against otherwise le
45                            The aqueous phase bacterial lysate was isolated in an array of microwells,
46 Ns into Escherichia coli expression vectors, bacterial lysates were found to be most suitable for in

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