mProX™ Human ACVRL1 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Generation of embryoid bodies (EBs).
To create embryoid bodies (EBs), ACVRL1wt/wt and ACVRL1wt/mut iPSCs were cultivated in a nonadherent environment. Endothelial differentiation was triggered when EBs got to be about 200 µm in diameter. The diameter of EBs was measured and their growth was tracked.
Ref: Xiang-Tischhauser, Li, et al. "Generation of a Syngeneic Heterozygous ACVRL1 (wt/mut) Knockout iPS Cell Line for the In Vitro Study of HHT2-Associated Angiogenesis." Cells 12.12 (2023): 1600.
Pubmed: 37371070
DOI: 10.3390/cells12121600
Research Highlights
Rendu-Osler-Weber (ROW) syndrome, also known as Hereditary Hemorrhagic Telangiectasia syndrome (HHT), is an autosomal dominant vascular condition. HHT1 and HHT2, the two most prevalent types of HHT, have been associated with mutations in the genes encoding endoglin (ENG) and activin receptor-like kinase 1 (ACVRL1 or ALK1), respectively.
Alaa el Din, Ferdos, et al. "Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia." PLoS One 10.7 (2015): e0132111.
Pubmed:
26176610
DOI:
10.1371/journal.pone.0132111
These findings imply that ALK1 expression in blood vessels is likewise susceptible to the AD pathophysiologic process, possibly connected to CAA, as previously shown for particular neuronal populations. However, in early and moderate AD, cerebral arterioles could still respond to ALK1 ligands like BMP9 and BMP10.
Anderson, Kelley E., et al. "The expression of Activin Receptor-Like Kinase 1 (ACVRL1/ALK1) in hippocampal arterioles declines during progression of Alzheimer's disease." Cerebral Cortex Communications 1.1 (2020): tgaa031.
Pubmed:
32974611
DOI:
10.1093/texcom/tgaa031