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1               Before labeling, the membranes were incubated with or without a highly charged sulfhydr
2                                 T cell lines were incubated with or without a sonicated heat-killed m
3                   As a negative control, DCs were incubated with or without an irrelevant control pro
4                                        Cells were incubated with or without androgens for 72 hours; t
5 oE and endogenous apoE on TGRP uptake, cells were incubated with or without apoE associated with (3)H
6  patients undergoing coronary bypass surgery were incubated with or without cytokines (interleukin-6/
7 rum samples from normals or patients with HF were incubated with or without exogenous nonglycosylated
8                                        RPTCs were incubated with or without IFN-gamma up to 48 h.
9  active systemic JIA, and 8 healthy controls were incubated with or without IFNgamma to gauge changes
10              Mouse stomach-derived organoids were incubated with or without inhibitors of WNT (DKK1)
11                                    HCE cells were incubated with or without MIP-133 at doses of 7.5,
12                                       ECV304 were incubated with or without native LDL (100 microgram
13 lood and BAL fluid samples from each subject were incubated with or without PPD, and the proportions
14 uman Raji lymphoma cells in log-phase growth were incubated with or without rituximab (20 microg/mL)
15 ells of the human leukemic cell line, HL-60, were incubated with or without the ornithine decarboxyla
16       Human umbilical vein endothelial cells were incubated with or without thrombin (1 U/mL) for 1 t
17         Injured or uninjured cartilage disks were incubated with or without TNFalpha and/or IL-6/sIL-
18 th stable CAD and 19 normal control subjects was incubated with or without various platelet agonists

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