Meanings
- uncountablebiochemistryA protein, characteristic of spastic paraplegia, that mediates autophagic lysosome reformation
1 more example
Antibodies used in this study include in-house antibodies against clathrin, AP-5 ζ (monoclonal antibody used for IF), µ5 and SPG11 monoclonal (4) and spastizin [PER antibody (49)] and commercial antibodies against spastizin (Atlas HPA035693), EEA1 (BD Transduction Labs E41120), LAMP1 (Abcam ab24170 and H4A3), CIMPR (2G11; Calbiochem 444105), AP-2 µ2 (AP50; BD Transduction Labs 611351), LC3 (4E12; MBL M152-3B), LBPA (Jean Gruenberg), CD63 (H5C6; BD Biosciences), tubulin (DM1A, Abcam ab7291) and actin (C4, Abcam ab3280).
2015 June 17, Jennifer Hirst et al., “Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease”, in Human Molecular Genetics, volume 24, →DOI
Cite this entry
spastizin. (n.d.). In WatkinsX Dictionary. Retrieved November 4, 2026, from https://dictionary.watkinsx.com/word/spastizin
“spastizin.” WatkinsX Dictionary, https://dictionary.watkinsx.com/word/spastizin. Accessed November 4, 2026.
WatkinsX Dictionary, s.v. “spastizin,” accessed November 4, 2026, https://dictionary.watkinsx.com/word/spastizin.
Source: spastizin on Wiktionary, CC BY-SA 4.0.