REM16 (Responsive to Embryo/Endosperm) is a member of the AP2/B3-like transcription factor family. It contains two B3 domains and regulates flowering time by directly activating key genes such as SOC1 (SUPPRESSOR OF OVEREXPRESSION OF CONSTANS) and FT (FLOWERING LOCUS T) .
Flowering Regulation:
Molecular Interactions:
REM16 interacts with ADF1 (actin-depolymerizing factor 1), suggesting a potential link between cytoskeletal dynamics and transcriptional regulation .
No specific DNA-binding sequence has been identified for REM16, aligning with the broader hypothesis that REM family proteins lack conserved DNA-binding motifs .
While REM16 itself is not associated with antibody research, the search results emphasize methodologies for antibody development and characterization. Below are key insights from antibody-focused studies that could inform hypothetical REM16 antibody projects:
If REM16 were targeted for antibody development, the following considerations would apply:
Immunohistochemistry: Localizing REM16 protein in Arabidopsis tissues during floral transition.
Western Blotting: Quantifying REM16 expression under different growth conditions.
ChIP Assays: Confirming REM16’s binding to SOC1/FT promoters .
Antigen Design: REM16’s B3 domains may lack immunogenic epitopes, requiring recombinant protein or peptide immunogens.
Cross-Reactivity: Antibodies must distinguish REM16 from other B3 domain-containing proteins.
Here’s a structured FAQ collection for researchers studying REM16 Antibody in academic contexts, synthesized from peer-reviewed studies and technical methodologies:
What computational tools analyze REM16 Antibody NGS data for epitope mapping?
Output: Clustered epitope regions with binding affinity scores (Table 1).
Table 1: REM16 Epitope Binding Profiles
How to resolve contradictions in REM16’s role across flowering pathways?
What orthogonal methods confirm REM16 Antibody specificity in structural studies?
How to standardize REM16 Antibody validation across labs?
What statistical models improve REM16 titer quantification in ELISA?