mProX™ Human MOS Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 Overexpression of Mos causes genomic instability in stable tetraploid cells.
Stable p53-deficient HCT 116 cells were transfected with a polycistronic plasmid expressing green fluorescent protein (GFP) alone or co-expressing Mos and GFP for 48 hours. The GFP-positive populations were purified using fluorescence-activated cell sorting (FACS), cultured for 48 hours, and subsequently subjected to repetitive transfections with the same constructs at approximately 5-day intervals. The columns represent the percentage of sub-tetraploid cells (mean±s.e.m., n=3 independent experiments) as determined after single (I) or multiple (II, III) rounds of transfection.
Ref: Vitale, Ilio, et al. "Multipolar mitosis of tetraploid cells: inhibition by p53 and dependency on Mos." The EMBO journal 29.7 (2010): 1272-1284.
Pubmed: 20186124
DOI: 10.1038/emboj.2010.11
Research Highlights
Liu, Qing-Yu. et al. "Solar-Driven Photothermal Catalytic Lignocellulosic Biomass-to-H2 Conversion." ACS applied materials & interfaces, 2023.
An effective conversion strategy is crucial for achieving sustainable use of lignocellulosic biomass, a promising source of chemical fuel. However, such strategies have been limited due to existing challenges. In this study, a novel approach involving photothermal catalysis using MoS2 and CeO2 was proposed for the selective conversion of lignocellulosic biomass. Results showed the potential of this method in overcoming the limitations of traditional conversion methods. This approach could significantly contribute to the sustainable utilization of lignocellulosic biomass.
Liu, Qing-Yu. et al. "Solar-Driven Photothermal Catalytic Lignocellulosic Biomass-to-H2 Conversion." ACS applied materials & interfaces, 2023.
Pubmed:
37871167
DOI:
10.1021/acsami.3c11091
Jiao, Guangzhong et al. "MOS mutation causes female infertility with large polar body oocytes." Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology vol. 38,12 (2022): 1158-1163.
The Moloney sarcoma oncogene (MOS) is known to encode a serine/threonine kinase protein and is highly expressed in oocytes undergoing meiotic maturation. This pathway, MOS/MAPK, typically plays a crucial role in maintaining the metaphasic state of microtubules and chromatin during meiotic divisions. To investigate the genetic factors behind female infertility linked to large polar body oocytes, the researchers conducted whole-exome sequencing on the patient and their family members, uncovering a previously unidentified homozygous missense mutation (c.591T> G) in MOS. Bioinformatics analysis confirmed the deleterious nature of this mutation, implicating it in the development of oocytes with large polar bodies and compromised embryonic development. Furthermore, it was suggested that the MOS variant might influence oocyte asymmetric division via the MAPK/WAVE2/Arp2/3/actin signaling pathway, shedding light on its role in early human reproductive processes and offering potential genetic markers for personalized genetic counseling and treatments.
Jiao, Guangzhong et al. "MOS mutation causes female infertility with large polar body oocytes." Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology vol. 38,12 (2022): 1158-1163.
Pubmed:
36403623
DOI:
10.1080/09513590.2022.2147158