3 research outputs found
Identification of novel proteins affected by rotenone in mitochondria of dopaminergic cells-4
<p><b>Copyright information:</b></p><p>Taken from "Identification of novel proteins affected by rotenone in mitochondria of dopaminergic cells"</p><p>http://www.biomedcentral.com/1471-2202/8/67</p><p>BMC Neuroscience 2007;8():67-67.</p><p>Published online 16 Aug 2007</p><p>PMCID:PMC2000881.</p><p></p>ded onto an 8–16% SDS-PAGE and analyzed by WB with indicated antibodies against marker proteins from mitochondria, cytosol, or nucleus. Antibodies against α-tubulin and nucleolin were used as markers for cytosolic and nuclear fractions, respectively. Antibodies directed against cytochrome C were used as markers for mitochondrial fraction
Identification of novel proteins affected by rotenone in mitochondria of dopaminergic cells-0
<p><b>Copyright information:</b></p><p>Taken from "Identification of novel proteins affected by rotenone in mitochondria of dopaminergic cells"</p><p>http://www.biomedcentral.com/1471-2202/8/67</p><p>BMC Neuroscience 2007;8():67-67.</p><p>Published online 16 Aug 2007</p><p>PMCID:PMC2000881.</p><p></p>ded onto an 8–16% SDS-PAGE and analyzed by WB with indicated antibodies against marker proteins from mitochondria, cytosol, or nucleus. Antibodies against α-tubulin and nucleolin were used as markers for cytosolic and nuclear fractions, respectively. Antibodies directed against cytochrome C were used as markers for mitochondrial fraction
Identification of novel proteins affected by rotenone in mitochondria of dopaminergic cells-1
<p><b>Copyright information:</b></p><p>Taken from "Identification of novel proteins affected by rotenone in mitochondria of dopaminergic cells"</p><p>http://www.biomedcentral.com/1471-2202/8/67</p><p>BMC Neuroscience 2007;8():67-67.</p><p>Published online 16 Aug 2007</p><p>PMCID:PMC2000881.</p><p></p>dance changes after rotenone treatment were classified into the following categories: folding degradation stability, metabolism, morphology, respiratory chain, protein synthesis, signaling, transport, miscellaneous, and unknown functions. For a protein with multiple functions, it is assigned to the one that is best known. While this chart reflects the group as a whole, the distribution was the same regardless of response to rotenone. Functional classification of proteins for each of the four groups shown in Table 1 (ASAPRatio = 0, ≥ 2.0, ≤ 0.5, or = 999) resulted in distributions that were not different from each other (χhad P > 0.05 for the four groups)