Discover top-quality products tailored for scientific and medical research. Request a personalized quote today
to enhance your projects.
Species | Human |
Cat.No | AM2481 |
Product Category | MicroRNA Agomir/Antagomir |
Size/Quantity | 2 OD, 4 OD, 50 OD (size by request, 1 OD corresponds to 33 ug) |
Shipping Info | Room Temperature |
Storage | -20°C / -80°C |
Product Type | microRNA Agomir/Antagomir |
Label | FAM, CY3, CY5, etc. (optional) |
Component | hsa-miR-653-5p Agomir and/or Antagomir (Product Form: Dry Powder) |
Key Features | *cover all human, mouse, and rat miRNAs listed in miRBase |
MIRacle™ hsa-miR-653-5p miRNA Agomir/Antagomir is a chemically modified synthetic oligonucleotide developed to precisely modulate the activity of endogenous microRNAs. The Agomir functions as a miRNA mimic, effectively enhancing the expression and biological activity of hsa-miR-653-5p. Whereas the Antagomir serves as a sequence-specific antagonist, inhibiting hsa-miR-653-5p function. Both formulations are optimized for high stability and efficacy in in vitro and in vivo settings. AcceGen provides the MIRacle™ series in multiple specifications (2 OD, 4 OD, 50 OD) with HPLC purification to accommodate a diverse range of experimental requirements. These reagents are ideal for exploring the biological functions of hsa-miR-653-5p in disease contexts such as prostate cancer metastasis, osteoarthritis progression via chondrocyte senescence regulation, and breast cancer suppression.
When you publish your research, please cite our product as “AcceGen Biotech Cat.# XXX-0000”. In return, we’ ll give you a $100 coupon. Simply click here and submit your paper’ s PubMed ID (PMID).
MIRacle™ hsa-miR-653-5p Agomir and Antagomir are optimized tools for modulating miR-653-5p activity with high stability and cellular uptake. The Agomir mimics endogenous miR-653-5p, enhancing its function, while the Antagomir binds complementarily to inhibit it. These reagents are ideal for studying miR-653-5p’s role in regulating EMT, apoptosis, and inflammatory pathways. Relevant disease contexts include prostate cancer metastasis, breast cancer suppression, and osteoarthritis via chondrocyte senescence. Their versatility in both in vitro and in vivo applications makes them essential for functional miRNA studies.