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1 resent in both the high salt-extractable and RIPA-resistant, SDS-extractable fraction in young human
2 induced IRF-3-mediated pathway of apoptosis (RIPA).
3 o extraction by both Triton X-100 as well as RIPA buffers.
4              Radioimmunoprecipitation assay (RIPA) and CBA were used to test for standard AChR antibo
5          The radioimmunoprecipitation assay (RIPA) has been used as a confirmatory test in several on
6  P protein in a partially denaturing buffer (RIPA) and a physiological buffer (IPP150).
7                            Thus, we compared RIPA with two indirect hemagglutination assays (Biolab D
8 ry test, few studies are available comparing RIPA to commercially available serologic test methods.
9 en compared with several other test formats, RIPA demonstrated equivalent or superior rates of agreem
10 rted that the pathway of IRF-3 activation in RIPA was independent of and distinct from the known path
11 ls treated for 5 to 60 minutes were lysed in RIPA buffer and subjected to Western blot with phospho (
12 en the activated T-lymphocytes were lysed in RIPA buffer containing anti-GraB, no proteolytic process
13 eal and conjunctival epithelia were lysed in RIPA buffer for Western blot with MAPK antibodies, or th
14 ls treated for 5 to 60 minutes were lysed in RIPA buffer for Western blot with phospho-specific antib
15 ormation of P but were exposed when P was in RIPA.
16 noprecipitated in vitro translated P well in RIPA, but three immunoprecipitated P poorly in IPP150.
17 A detected antibodies in 38.1% (16 of 42) of RIPA-negative patients with MG with 100% specificity.
18 useful procedure in the routine diagnosis of RIPA-negative MG, particularly in children.
19                      To evaluate the role of RIPA in viral pathogenesis, we engineered a genetically
20 tibody detected by radioimmunoprecipitation (RIPA) was > or =401.
21  of protection against disease and show that RIPA is most sensitive for detection of early vaccine-in
22       In particular, at titers of >1:40, the RIPA compared favorably with other test methods currentl
23  considerably among the tests, with only the RIPA and the Organon and Gull assays identifying reactiv
24 ed in vitro, and lysates were prepared using RIPA buffer which contains 1% Nonidet P-40, 0.5% deoxych
25 use, which expressed a mutant IRF-3 that was RIPA-competent but transcriptionally inert; this single-

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