| Code | CSB-RA056935A0HU |
| Size | US$210 |
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| Application | Recommended Dilution |
|---|---|
| WB | 1:500-1:2000 |
| IF | 1:50-1:200 |
| FC | 1:50-1:200 |
SMAD1 serves as a critical intracellular signal transducer in the bone morphogenetic protein (BMP) signaling pathway, playing essential roles in embryonic development, cell differentiation, and tissue homeostasis. As a receptor-regulated SMAD, it becomes phosphorylated upon BMP receptor activation and subsequently translocates to the nucleus to regulate target gene expression. This central position in BMP signaling makes SMAD1 a key target for researchers investigating developmental biology, stem cell differentiation, bone formation, and various disease processes including cancer and fibrosis.
This recombinant monoclonal antibody, clone 8G10, offers the reproducibility and consistency that demanding experimental workflows require. Generated against a synthetic peptide from human SMAD1, the recombinant production method ensures sequence-defined specificity and eliminates the lot-to-lot variability that can compromise longitudinal studies or multi-site collaborations.
Validation across multiple applications demonstrates this antibody's experimental flexibility. Western blot analysis successfully detects SMAD1 in U-87MG glioblastoma, A549 lung carcinoma, and HEK293 cell lysates, with an observed band at approximately 50 kDa. The slight difference from the predicted 52 kDa molecular weight likely reflects post-translational processing or variations in gel migration conditions. Immunofluorescence staining in HeLa cells reveals clear intracellular localization patterns, while flow cytometry analysis in Jurkat cells shows distinct positive signal separation from isotype controls, confirming utility for quantitative single-cell analyses.
Whether investigating BMP-mediated differentiation programs, characterizing SMAD1 expression across cell populations, or examining subcellular localization dynamics, this antibody provides researchers with a reliable tool for exploring this fundamental signaling pathway across diverse experimental platforms.
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