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1 rations of (oo)cysts, we used filtration and immunomagnetic separation.
2 tes, microglia, and RGCs were prepared using immunomagnetic separation.
3  (QDs) as a fluorescence marker coupled with immunomagnetic separation.
4 nmental water via vortex flow filtration and immunomagnetic separation.
5  the interleukin 2 receptor) were removed by immunomagnetic separation.
6 formed with CD34+ cell fractions enriched by immunomagnetic separation.
7 bacteria are isolated and concentrated using immunomagnetic separation.
8 uorimmunoassay (MMCIA) is described using an immunomagnetic separation and a fluorescent microplate t
9 functional T cell subsets were determined by immunomagnetic separation and flow immunocytometric anal
10          An integrated system with automated immunomagnetic separation and processing of fluidic samp
11                BChE adducts are extracted by immunomagnetic separation and proteolyzed with pepsin yi
12 icable to the multitude of assays comprising immunomagnetic separation, as a tool to establish quanti
13  electrochemical detection together with the immunomagnetic separation confers high sensitivity, resu
14 d sensitive detection of Salmonella based on immunomagnetic separation, fluorescence labeling and sma
15 t for tumor cells, we tested the efficacy of immunomagnetic separation for enriching fixed solid tumo
16                                              Immunomagnetic separation has become an essential tool f
17  Macrophages isolated from damaged nerves by immunomagnetic separation (IMS) and stimulated with IL-4
18 ed to overnight broth enrichment followed by immunomagnetic separation (IMS) and to direct plating of
19 osomes are preconcentrated from the serum by immunomagnetic separation (IMS) based on a CD326 recepto
20 -based analytical device (PAD) combined with immunomagnetic separation (IMS) for detecting Salmonella
21 e, we have devised an approach that combines immunomagnetic separation (IMS) for targeted bacterial e
22                        Our protocol combines immunomagnetic separation (IMS) for targeted bacterial e
23                 An automated high-throughput immunomagnetic separation (IMS) method for diagnosing ex
24 ribes the development and optimization of an immunomagnetic separation (IMS) method to isolate Mycoba
25 his creates a challenge for using bead-based immunomagnetic separation (IMS) that typically enriches
26                    FMNBs probes also provide immunomagnetic separation (IMS) to enrich the analysts a
27 tion of stx(1) and stx(2) Shiga toxin genes, immunomagnetic separation (IMS), and selective culture e
28                                          The immunomagnetic separation increased the sensitivity of t
29                                              Immunomagnetic separation is a highly specific technique
30                                              Immunomagnetic separation is effective for the enrichmen
31                  Coupled with a large-volume immunomagnetic separation method, LOD for spiked lettuce
32 d adducts in serum samples were processed by immunomagnetic separation of BChE by antibody conjugated
33 red using a semiautomated technique based on immunomagnetic separation of epithelial cell adhesion mo
34                    These new methods include immunomagnetic separation of pathogen, PCR amplification
35                                              Immunomagnetic separation of thymocytes revealed that th
36                 By broth enrichment culture, immunomagnetic separation, or both, 35 cattle had 1 posi
37                  CTCs were measured using an immunomagnetic separation technique.
38  To address this issue, we have developed an immunomagnetic separation technology that can quickly so
39 tion to disassemble pathogens from the meat, immunomagnetic separation to purify meat samples and ind
40  eight TIPS retrieved from liver explants by immunomagnetic separation using monodispersed magnetizab
41                                              Immunomagnetic separation was effective in unembedded fi
42                                              Immunomagnetic separation was then used to select c-kit-
43                                   A specific immunomagnetic separation was used to capture the progen
44 directly in human serum, when performing the immunomagnetic separation with antiCD81 modified magneti
45 d and labeled from 100 muL of whole blood by immunomagnetic separation with magnetic particles modifi
46  the combination of the SPR spectroscopy and immunomagnetic separation with using gold-coated magneti