| Published Application/Species/Sample/Dilution | Reference |
|---|
- western blot; human; 1:300; loading ...; fig 4b
| O'Grady G, Best H, Sztal T, Schartner V, Sanjuan-Vazquez M, Donkervoort S, et al. Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization. Am J Hum Genet. 2016;99:1086-1105 pubmed publisher |
- immunocytochemistry; human; 1:500; fig 2
- western blot; human; 1:500; fig 9
| Eisch V, Lu X, Gabriel D, Djabali K. Progerin impairs chromosome maintenance by depleting CENP-F from metaphase kinetochores in Hutchinson-Gilford progeria fibroblasts. Oncotarget. 2016;7:24700-18 pubmed publisher |
- immunocytochemistry; mouse; 1:50; fig s2d
| Fuchs C, Gawlas S, Heher P, Nikouli S, Paar H, Ivankovic M, et al. Desmin enters the nucleus of cardiac stem cells and modulates Nkx2.5 expression by participating in transcription factor complexes that interact with the nkx2.5 gene. Biol Open. 2016;5:140-53 pubmed publisher |
- western blot; mouse; 1:5000
| Tapia O, Fong L, Huber M, Young S, Gerace L. Nuclear envelope protein Lem2 is required for mouse development and regulates MAP and AKT kinases. PLoS ONE. 2015;10:e0116196 pubmed publisher |
- immunohistochemistry; mouse; 1:200
| Jung H, Tatar A, Tu Y, Nobumori C, Yang S, Goulbourne C, et al. An absence of nuclear lamins in keratinocytes leads to ichthyosis, defective epidermal barrier function, and intrusion of nuclear membranes and endoplasmic reticulum into the nuclear chromatin. Mol Cell Biol. 2014;34:4534-44 pubmed publisher |
| Vaajanen A, Kalesnykas G, Vapaatalo H, Uusitalo H. The expression of Mas-receptor of the renin-angiotensin system in the human eye. Graefes Arch Clin Exp Ophthalmol. 2015;253:1053-9 pubmed publisher |
| Mewborn S, Puckelwartz M, Abuisneineh F, Fahrenbach J, Zhang Y, MacLeod H, et al. Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation. PLoS ONE. 2010;5:e14342 pubmed publisher |
| Verstraeten V, Caputo S, van Steensel M, Duband-Goulet I, Zinn-Justin S, Kamps M, et al. The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress. J Cell Mol Med. 2009;13:959-71 pubmed publisher |
| Boudreau E, Labib S, Bertrand A, Decostre V, Bolongo P, Sylvius N, et al. Lamin A/C mutants disturb sumo1 localization and sumoylation in vitro and in vivo. PLoS ONE. 2012;7:e45918 pubmed publisher |
| Ho C, Jaalouk D, Vartiainen M, Lammerding J. Lamin A/C and emerin regulate MKL1-SRF activity by modulating actin dynamics. Nature. 2013;497:507-11 pubmed publisher |
