eIF3M inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the eukaryotic translation initiation factor 3 subunit M (eIF3M). eIF3M is a component of the eIF3 complex, which is a crucial player in the initiation phase of eukaryotic translation. The eIF3 complex is the largest and most complex of the translation initiation factors, composed of multiple subunits, including eIF3M. This complex plays a critical role in the recruitment of the small ribosomal subunit to the mRNA, the scanning of the mRNA for the start codon, and the assembly of the translation machinery. Inhibiting eIF3M can disrupt the overall function of the eIF3 complex, thereby impeding the translation initiation process. This makes eIF3M inhibitors important tools in research for studying the specific role of this subunit in translation and its broader impact on protein synthesis.
The study of eIF3M inhibitors provides valuable insights into the mechanistic aspects of translation initiation. By selectively inhibiting eIF3M, researchers can dissect the specific contributions of this subunit to the eIF3 complex's function and its interaction with other components of the translation machinery. This approach allows scientists to explore how eIF3M influences the regulation of gene expression at the translational level, as well as its involvement in various cellular processes that depend on efficient protein synthesis. Furthermore, eIF3M inhibitors can help identify potential regulatory networks that modulate the activity of the eIF3 complex, offering a deeper understanding of how cells control protein production under different physiological conditions. Overall, eIF3M inhibitors are essential tools for advancing our knowledge of translation initiation and the complex molecular mechanisms that govern this fundamental process in eukaryotic cells.
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디스플레이 라벨:
| 제품명 | CAS # | 카탈로그 번호 | 수량 | 가격 | 引用 | RATING |
|---|---|---|---|---|---|---|
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $57.00 $182.00 $92.00 | 21 | |
캠토테신과 프라임이 토포이소머라제 I을 억제하면 DNA 손상이 발생하여 RNAi 과정에 대한 집중력이 감소하고 결과적으로 eIF2C2 발현이 감소할 수 있습니다. | ||||||
Geldanamycin | 30562-34-6 | sc-200617B sc-200617C sc-200617 sc-200617A | 100 µg 500 µg 1 mg 5 mg | $38.00 $58.00 $102.00 $202.00 | 8 | |
겔다나마이신은 Hsp90을 억제함으로써 RNAi와 관련된 단백질을 불안정하게 만들 수 있으며, 이는 eIF2C2 안정성 또는 합성의 감소를 포함할 수 있습니다. | ||||||
Silvestrol | 697235-38-4 | sc-507504 | 1 mg | $920.00 | ||
식물 아글레이아 포베올라타에서 분리한 천연 화합물로, EIF4AI를 강력하게 억제하는 것으로 알려져 있습니다. | ||||||
Rocaglamide | 84573-16-0 | sc-203241 sc-203241A sc-203241B sc-203241C sc-203241D | 100 µg 1 mg 5 mg 10 mg 25 mg | $270.00 $465.00 $1607.00 $2448.00 $5239.00 | 4 | |
아글레이아 속과 같은 여러 식물에서 발견되는 또 다른 천연 화합물로 강력한 EIF4AI 억제 활성을 가지고 있습니다. | ||||||