mProX™ Human ACVR1B Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number
Made to Order Inquiry
InquiryProduct Information
Product Properties
Protocols
Please visit our protocols page.
Customer Reviews
George
Verified Customer
Carol
Verified Customer
Any questions about our products? Please visit our frequently asked questions page.
Published Data
Fig.1 Expression of ACVR1B and SMAD4 in PC cell lines.
mRNA expression levels of the SMAD4 and ACVR1B genes in PC cell lines and normal pancreatic tissue (RNA from Clontech). Real-time RT-PCR was used to assess the expressions. The Sui65, Sui68, and Sui71 cell lines showed very little expression of ACVR1B mRNA, while the Sui65, Sui70, and Sui71 cell lines showed very little expression of SMAD4 mRNA.
Ref: Togashi, Yosuke, et al. "Homozygous deletion of the activin A receptor, type IB gene is associated with an aggressive cancer phenotype in pancreatic cancer." Molecular cancer 13.1 (2014): 1-15.
Pubmed: 24886203
DOI: 10.1186/1476-4598-13-126
Research Highlights
According to these findings, activin A enhances the neurological prognosis of ischemic stroke-affected mice by stimulating oligodendroglial ACVR1B-mediated white matter remyelination, which may offer an effective treatment approach.
Zheng, Jiayin, et al. "Activin A improves the neurological outcome after ischemic stroke in mice by promoting oligodendroglial ACVR1B-mediated white matter remyelination." Experimental Neurology 337 (2021): 113574.
Pubmed:
33345977
DOI:
10.1016/j.expneurol.2020.113574
Atrophy and muscle wasting disorders in skeletal muscle are associated with growth factors belonging to the transforming growth factor-β (TGF-β) family, including TGF-β1 and myostatin.
Hillege, Michèle MG, et al. "Lack of Tgfbr1 and Acvr1b synergistically stimulates myofibre hypertrophy and accelerates muscle regeneration." Elife 11 (2022): e77610.
Pubmed:
35323108
DOI:
10.7554/eLife.77610