

| Catalog No. | MV489014 | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Species reactivity | Human, Mouse | ||||||||
| Applications | ELISA, IHC, WB | ||||||||
| Host species | Rabbit | ||||||||
| Isotype | IgG | ||||||||
| Clonality | Polyclonal | ||||||||
| Immunogen | E. coli - derived recombinant Mouse METTL3 (Asp366-Leu580). | ||||||||
| Target | N6-adenosine-methyltransferase subunit METTL3, 2.1.1.348, Methyltransferase-like protein 3, N6-adenosine-methyltransferase 70 kDa subunit, MT-A70, Mettl3, Mta70 | ||||||||
| Purification | Purified by antigen affinity column. | ||||||||
| Accession | Q8C3P7 | ||||||||
| Form | Liquid | ||||||||
| Storage buffer | 0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300. Please refer to the specific buffer information in the hardcopy of datasheet or the lot-specific COA. |
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| Product Usage Information |
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| Stability and Storage | Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt. | ||||||||
| Background | N(6)-adenosine-methyltransferase catalytic subunit METTL3 is a ~64 kDa protein. The METTL3-METTL14 heterodimer forms a N6-methyltransferase complex that methylates adenosine residues at the N(6) position of some RNAs and regulates various processes such as the circadian clock, differentiation of embryonic and hematopoietic stem cells, cortical neurogenesis, response to DNA damage, differentiation of T-cells and primary miRNA processing. In the heterodimer formed with METTL14, METTL3 constitutes the catalytic core. N6-methyladenosine (m6A), which takes place at the 5'-[AG]GAC-3' consensus sites of some mRNAs, plays a role in mRNA stability, processing, translation efficiency and editing. M6A acts as a key regulator of mRNA stability: methylation is completed upon the release of mRNA into the nucleoplasm and promotes mRNA destabilization and degradation. In embryonic stem cells (ESCs), m6A methylation of mRNAs encoding key naive pluripotency-promoting transcripts results in transcript destabilization, promoting differentiation of ESCs. 1. Wang, Y. et al. (2014) Nature cell biology 16, 191-8. PMID: 24394384 2. Batista, PJ. et al. (2014) Cell stem cell 15, 707-19. PMID: 25456834 3. Geula, S. et al. (2015) Science (New York, N.Y.) 347, 1002-6. PMID: 25569111 4. Li, HB. et al. (2017) Nature 548, 338-342. PMID: 28792938 5. Xu, K. et al. (2017) Cell research 27, 1100-1114. PMID: 28809392 6. Zhang, C. et al. (2017) Nature 549, 273-276. PMID: 28869969 7. Yoon, KJ. et al. (2017) Cell 171, 877-889.e17. PMID: 28965759 8. Ke, S. et al. (2017) Genes & development 31, 990-1006. PMID: 28637692 | ||||||||
| Note | For research use only. |
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