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