mProX™ Human BMPR1B Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Results of luciferase activity analyses.
The assay results showed that co-transfection with miR-1306 mimics significantly decreased the luciferase activity in cells containing the wild-type vector, suggesting that miR-1306 can suppress the transcriptional activity of the 3'-UTR region of BMPR1B.
Ref: Abdurahman, Anwar, et al. "miR-1306 induces cell apoptosis by targeting BMPR1B gene in the ovine granulosa cells." Frontiers in Genetics 13 (2022): 989912.
Pubmed: 36212145
DOI: 10.3389/fgene.2022.989912
Research Highlights
Of women under 40, 1% suffer from the often occurring condition known as primary ovarian insufficiency (POI). Infertility results from POI, which is characterized by early ovarian follicle depletion and increased follicle-stimulating hormone plasma levels.
Renault, Lucie, et al. "BMPR1A and BMPR1B missense mutations cause primary ovarian insufficiency." The Journal of Clinical Endocrinology & Metabolism 105.4 (2020): e1449-e1457.
Pubmed:
31769494
DOI:
10.1210/clinem/dgz226
One of the primary genes that can be employed as a molecular genetic marker for the early selection of ewes with high productivity is BMPRIB. The initial mutation in the kinase domain of the BMPR1B gene, p.Q249R (g.746A> G), is well-documented and strongly associated with higher ovulation rate and litter size.
Akhatayeva, Zhanerke, et al. "Survey of the relationship between polymorphisms within the BMPR1B gene and sheep reproductive traits." Animal Biotechnology 34.3 (2023): 718-727.
Pubmed:
34586970
DOI:
10.1080/10495398.2021.1979023