Detection of p62/SQSTM1 Aggregates in Cellular Models of CCM Disease by Immunofluorescence.
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DOI: 10.1007/978-1-0716-0640-7_30
Abstract: Cerebral cavernous malformations (CCM) is a familial or sporadic rare disorder that is characterized by capillary vascular lesions with a mulberry-like appearance on MRI scans. Three distinct genes have been associated to CCM disease, known… read more here.
Keywords: p62 sqstm1; immunofluorescence; ccm disease; detection p62 ... See more keywords
Spectrophotometric Method for Determining Glyoxalase 1 Activity in Cerebral Cavernous Malformation (CCM) Disease.
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DOI: 10.1007/978-1-0716-0640-7_33
Abstract: Glyoxalase 1 (Glo1) is a glutathione (GSH)-dependent enzyme that catalyzes the isomerization of the hemithioacetal formed non-enzymatically from methylglyoxal (MG) and GSH to S-D-lactoylglutathione (SLG). The activity of Glo1 is measured spectrophotometrically by following the… read more here.
Keywords: glyoxalase; ccm disease; malformation ccm; cerebral cavernous ... See more keywords