PSMB2 and RPL32 are suitable denominators to normalize gene expression profiles in bronchoalveolar cells1 Department of Immunology, Palacky University, The Czech Republic 2 Department of Respiratory Medicine, Palacky University & Faculty Hospital, Olomouc, The Czech Republic 3 Interstitial Lung Disease Unit, Royal Brompton Hospital, London, UK
BMC Molecular Biology 2008, 9:69doi:10.1186/1471-2199-9-69
Additional filesAdditional file 1: Description of used statistical approaches. Format: DOC Size: 89KB Download file This file can be viewed with: Microsoft Word Viewer Additional file 2: Table E1. Clinical and laboratory characteristics of investigated subjects. Format: DOC Size: 57KB Download file This file can be viewed with: Microsoft Word Viewer Additional file 3: Definition of terms. Format: DOC Size: 33KB Download file This file can be viewed with: Microsoft Word Viewer Additional file 4: Figure E1. RNA quality assessment (a representative example) by 2100 Bioanalyzer (Agilent Technologies, Palo Alto, USA). This figure shows typical chromatogram of microcapillary electrophoresis of total RNA preparation of good quality extracted from bronchoalveolar lavage cells. Electropherogram shows 18S and 28S rRNA peaks. FU – Fluorescence units. Format: DOC Size: 200KB Download file This file can be viewed with: Microsoft Word Viewer Additional file 5: Figure E2. Expression levels of ten housekeeping genes in bronchoalveolar cells from sarcoidosis patients and normal subjects from the 2nd cohort. Expression levels of ten housekeeping genes in CTt values in bronchoalveolar cells from sarcoidosis patients (n = 63) a normal subjects (n = 17). The data are presented as means (columns) ± SD (errorbars). White columns represent the control group, dark columns sarcoidosis patients. Format: DOC Size: 731KB Download file This file can be viewed with: Microsoft Word Viewer |




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