mProX™ Human BMPR2 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
Lisa
Verified Customer
Brian
Verified Customer
Any questions about our products? Please visit our frequently asked questions page.
Published Data
Fig.1 Loss of BMPR2 potentiated activin-induced ALK2 activity.
It was possible to create myeloma cell lines that expressed shRNAs, shCTR (non-targeting), shBMPR2, or shALK1. Using the comparative Ct-method, the expression of BMPR2 mRNA in relation to GAPDH in the cell lines was ascertained in INA-6 and IH-1.
Ref: Olsen, Oddrun Elise, et al. "BMPR2 inhibits activin and BMP signaling via wild-type ALK2." Journal of cell science 131.11 (2018): jcs213512.
Pubmed: 29739878
DOI: 10.1242/jcs.213512
Research Highlights
Compared to patients without BMPR2 mutations, those with PAH and BMPR2 mutations appear at a younger age with a more severe disease and are at a higher risk of dying or requiring a transplant.
Evans, Jonathan DW, et al. "BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis." The lancet Respiratory medicine 4.2 (2016): 129-137.
Pubmed:
26795434
DOI:
10.1016/S2213-2600(15)00544-5
This review compiled the most recent research on the molecular underpinnings of BMPR2's roles in BMP signaling as well as the diversity of those activities. Aspects of BMPR2 pathogenic mutations that have been experimentally verified and the associated human disorders will also be covered. These topics are crucial for diagnosis and therapy in clinical settings.
Kim, Myung-Jin, et al. "Clinical significance linked to functional defects in bone morphogenetic protein type 2 receptor, BMPR2." BMB reports 50.6 (2017): 308.
Pubmed:
28391780
DOI:
10.5483/bmbrep.2017.50.6.059