This antibody targets a plant-specific microtubule-associated protein (MAP) that regulates cortical microtubule orientation and subsequent organ growth direction. It modulates microtubule severing, thereby influencing microtubule organization.
Relevant Research:
Golgi-localized TORC1: Antibodies must distinguish between cytoplasmic and Golgi pools. In colorectal cancer, Rab1A-mTORC1 interactions occurred specifically in the Golgi, requiring high-resolution imaging .
Nuclear vs. cytoplasmic roles: Validate with fractionation assays. TOR1 regulates RNA Pol I localization in the nucleolus, necessitating nuclear-cytoplasmic separation .
Proximity ligation assays (PLA): Detect direct protein interactions in situ, reducing false positives from co-IP .
Single-cell RNA sequencing: Identify heterogeneity in TOR1 expression across cell populations, addressing variability in bulk assays .
CRISPR-Cas9 tagging: Endogenously tag TOR1 to bypass antibody limitations in certain models .
Epitope mapping: Compare conserved regions across species. For example, TbTOR1 shares 28% identity with human mTOR, requiring custom antibody validation .
Cross-validation: Use orthogonal methods (e.g., metabolic labeling for protein synthesis) to confirm antibody-based findings .
Phosphorylation at regulatory sites (e.g., Ser/Thr residues) can alter epitope accessibility. Use phosphatase-treated lysates to assess modification-dependent binding .
Ubiquitination or SUMOylation may require specialized lysis buffers (e.g., inclusion of N-ethylmaleimide) .