24 research outputs found
MOESM3 of Modelling physiological and pathological conditions to study pericyte biology in brain function and dysfunction
Additional file 3: Table S3. List of antibodies used for ICC and flow cytometry. This table provides a list of antibodies used for the ICC and flow cytometry studies
MOESM4 of Modelling physiological and pathological conditions to study pericyte biology in brain function and dysfunction
Additional file 4: Table S4. List of primers used for qRT-PCR. This table lists the primers used for the qRT-PCR studies
MOESM2 of Modelling physiological and pathological conditions to study pericyte biology in brain function and dysfunction
Additional file 2: Table S2. List of BD Biosciences Flex Sets used for CBA. This table lists the BD Biosciences Flex Sets used for the CBA studies
MOESM1 of Modelling physiological and pathological conditions to study pericyte biology in brain function and dysfunction
Additional file 1: Table S1. In vitro culture conditions of brain pericytes in selected publications. This table lists previous publications describing in vitro pericyte cell culture conditions
Additional file 2: of Unique and shared inflammatory profiles of human brain endothelia and pericytes
Full secretome profiler dataset from Fig. 5. Pericytes or endothelia from two different cases were treated with either vehicle, or IL-1β (10 ng/mL) for 24 h before media were harvested and secretions analysed as per Fig. 5. Values represent intensity measurements from each secretion spot (two spots per secretion) from both biological replicates, from all treatment groups (Vehicle/Pericyte, IL-1β/Pericyte, Vehicle/Endothelial, IL-1β/Endothelial). Data are given in an Excel spreadsheet. (XLSX 41 kb
Full western blots for Fibrils, Ribbons, fibrils65, fibrils91, fibrils110 and no treatment control with AA103-108, AA124-134 and GAPDH.
Two blots used for each alpha synuclein strain. Each blot was labelled with α-syn antibodies (AA103-108 or AA124-134), imaged, stripped and relabelled for GAPDH. (PDF)</p
Life cell imaging (120 hours) of pericytes pre-treated for 4 hours with 100nM fibrils65-atto647.
(AVI)</p
Case information for post-mortem and surgical removedbrain tissue used in this study.
Case information for post-mortem and surgical removedbrain tissue used in this study.</p
Life cell imaging (90 hours) of mixed neuronal cell cultures pre-treated for 4 hours with 100nM fibrils110-atto647.
(AVI)</p