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1  elution from protein G and Galalpha1-3Gal-R immunoadsorbents.
2 tegrins was determined by cell enzyme-linked immunoadsorbent assay (ELISA) and immunoprecipitation.
3 pared with control cell lines, enzyme-linked immunoadsorbent assay (ELISA), immunoprecipitation, and
4 t cytotoxicity tests and by an enzyme-linked immunoadsorbent assay (ELISA).
5                                Enzyme-linked immunoadsorbent assay showed that the complex consisting
6 rified by Western blotting and enzyme-linked immunoadsorbent assay using specific antibodies.
7                     Second, an enzyme-linked immunoadsorbent assay was developed and used to measure
8 d by mixed leukocyte reaction, enzyme-linked immunoadsorbent assay, and ELISPOT assays.
9 factor (PlGF) were measured by enzyme-linked immunoadsorbent assay.
10 actor VEGF-C was quantified by enzyme-linked immunoadsorbent assay.
11 d VEGF levels were assessed by enzyme-linked immunoadsorbent assay.
12                 As assessed by enzyme-linked immunoadsorbent assays and ligand blot binding assays, m
13   A novel reagent for low-level detection in immunoadsorbent assays is described.
14  The peptide mixture was then purified on an immunoadsorbent column containing immobilized antibodies
15    In eluates from both patient and control, immunoadsorbent column immunoglobulins together with C3a
16 bolished after passage of serum over a CD200 immunoadsorbent column.
17              In two recipients, eluates from immunoadsorbent columns were analyzed for C3a, C1q, and
18                                          The immunoadsorbent could quantitatively remove the CR1-cont
19 ically active prior to being passed over the immunoadsorbent for EGF remained dimerized and enzymatic
20 ing EGF and then immediately passed over the immunoadsorbent for EGF.
21 EGF), was passed over a column containing an immunoadsorbent for EGF.
22                                          The immunoadsorbent removed both EGF free in solution and EG
23      The tryptic digests were passed over an immunoadsorbent specific for peptides with the amino-and
24 upled to macroporous glass beads, forming an immunoadsorbent that is mechanically and chemically stab
25                                           An immunoadsorbent that was specific for the carboxy-termin
26 125I]radioiodinated peptides isolated by the immunoadsorbent were submitted to high-pressure liquid c

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