| Code | CSB-RA109371A0HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:5000 |
| IF | 1:50-1:200 |
| FC | 1:50-1:200 |
DCP1A, also known as mRNA-decapping enzyme 1A, plays a central role in mRNA turnover by catalyzing the removal of the 5' cap structure, a critical step that commits transcripts to degradation. Beyond its function in mRNA decay, DCP1A also serves as a Smad4-interacting transcriptional co-activator (SMIF), linking it to TGF-β signaling pathways. This dual functionality makes DCP1A a compelling target for researchers investigating post-transcriptional gene regulation, stress granule dynamics, and cellular signaling networks.
This recombinant monoclonal antibody, generated in rabbit using clone 10E12, offers the reproducibility and consistency that demanding experimental workflows require. Because recombinant antibodies are produced from defined sequences, you can expect uniform performance across lots, eliminating the variability often encountered with traditional hybridoma-derived reagents. The antibody has been affinity-purified to ensure high specificity for its target.
Validation studies demonstrate robust performance across multiple applications. Western blot analysis detects a band at the predicted molecular weight of 63 kDa across diverse human cell lines including HeLa, HepG2, COLO-205, Jurkat, and K562, confirming reliable detection in both epithelial and hematopoietic cell contexts. For immunofluorescence microscopy, the antibody successfully visualizes DCP1A localization in SH-SY5Y neuroblastoma cells at dilutions of 1:50 to 1:200. Flow cytometry validation in Jurkat cells shows clear separation between specific signal and isotype control, enabling quantitative analysis of DCP1A expression at the single-cell level.
This antibody is well-suited for studies examining P-body formation, mRNA surveillance mechanisms, and the intersection of transcriptional regulation with mRNA decay pathways in human cell systems.
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