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1 ssay, indirect immunofluorescence (IIF), and immunodiffusion.
2 cal methods, such as complement fixation and immunodiffusion.
3  performed by immunoprecipitation and double immunodiffusion.
4 subclass levels were determined using radial immunodiffusion.
5  to that of the LOS, as determined by double immunodiffusion.
6 e presence of antibodies to FCS using double immunodiffusion.
7 hat of the LOS alone as determined by double immunodiffusion.
8 ncentrations were determined by using radial immunodiffusion.
9 n 678 samples using the gold standard radial immunodiffusion.
10  immunoassay (EIA), complement fixation, and immunodiffusion.
11 es, predominantly by a standardized agar gel immunodiffusion (AGID) assay in centralized reference la
12 y offers improved sensitivity, compared with immunodiffusion and complement fixation, is not impaired
13 particles was further confirmed using double immunodiffusion, and association of LBP and FHRP in plas
14 rinogen levels were determined by the radial immunodiffusion assay (RID).
15 lated the reactivity of the antiserum in the immunodiffusion assay for CF antibody.
16  CRP serum levels were assessed using radial immunodiffusion assay in 174 subjects, 59 with moderate
17 emagglutination inhibition (HI) and agar gel immunodiffusion assays, and inability to productively re
18 globin, and albumin concentrations by radial immunodiffusion assays.
19 sease is endemic and 44 cases were tested by immunodiffusion at MiraVista Diagnostics.
20 he coccidioidal complement fixation (CF) and immunodiffusion-CF antigen.
21 hitinase and a line of identity with control immunodiffusion-CF-positive antigen.
22 ulmonary histoplasmosis in this assay, while immunodiffusion, complement fixation, and antigen testin
23 se of the commercially available antigens in immunodiffusion-complement fixation tests.
24 that the RBP EIA correlates well with radial immunodiffusion for RBP and with HPLC for retinol, the c
25 8 (92.7%) patients with a positive result by immunodiffusion (ID) and/or complement fixation (CF) had
26 performances of complement fixation (CF) and immunodiffusion (ID) assays for anti-Histoplasma antibod
27 CF antigen formed a line of identity with an immunodiffusion (ID) CF reference antigen (coccidioidin)
28     The sensitivity of antibody detection by immunodiffusion (ID) was 84.2%.
29  Results from nuclear magnetic resonance and immunodiffusion identified each of 16 polysaccharides as
30 unoassay (EIA), complement fixation (CF) and immunodiffusion (IMDF).
31 itive in 7%, antibodies were demonstrated by immunodiffusion in 67% and complement fixation in 70%, a
32    Immunocytochemical studies carried out by immunodiffusion on rat lung with an anti-PV-1 polyclonal
33 weeks in a process similar to an Ouchterlony immunodiffusion precipitate.
34 ociations between newer methods and standard immunodiffusion results were evaluated.
35 d either as thrombin-clottable protein or by immunodiffusion revealed a fibrinogen level ranging betw
36 HA quantification based on the single radial immunodiffusion (SRID) assay, which is time-consuming, l
37 ral vaccines is assayed by the single radial immunodiffusion (SRID) method.
38 xamined the sensitivity of the single radial immunodiffusion (SRID) potency test to differences in HA
39 ed, and the sensitivity of the single radial immunodiffusion (SRID) potency test to glycosylation was
40  sera preparation for use with single-radial immunodiffusion (SRID), the accepted vaccine potency ass
41           As an alternative to Single Radial Immunodiffusion (SRID), we report a new quantitative enz
42 nt with confirmed coccidioidal infection, an immunodiffusion test for CF antigenicity, and substrate
43                  The RT-nPCR assay, agar gel immunodiffusion test, and conventional virus isolation w
44 e values for PCR, serology using an agar gel immunodiffusion test, and tracheal wash fluid culture.
45                                          The immunodiffusion tests detected P.marneffei antigenemia i
46                      In this group, standard immunodiffusion tests of unconcentrated sera were positi
47                      Complement fixation and immunodiffusion tests performed on the patient's serum w
48  available, we attempted to develop separate immunodiffusion tests to detect P. marneffei antigens an
49 pture enzyme-linked immunosorbent assay, and immunodiffusion tests, MAb C3.1 is an IgG3 isotype.
50 antibodies could not be detected by agar gel immunodiffusion until 20 to 23 days p.i.
51                           The sensitivity of immunodiffusion was 60.2%, and the specificity was 98.8%
52       Analysis of culture filtrate by double immunodiffusion yielded a single line of immunoprecipita