UGT91C1 Antibody

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Product Specs

Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
UGT91C1 antibody; At5g49690 antibody; K2I5.5 antibody; UDP-glycosyltransferase 91C1 antibody; EC 2.4.1.- antibody
Target Names
UGT91C1
Uniprot No.

Q&A

FAQs for UGT91C1 Antibody in Academic Research

Advanced Research Questions

  • How to resolve contradictions in UGT91C1 subcellular localization data?

    • Hypothesis testing:

      TechniqueLocalization ReportedConflict Resolution Strategy
      ICC/IFCytoplasmic Use compartment-specific markers (e.g., ER-Tracker)
      FractionationNuclear Verify purity of subcellular fractions via organelle-specific antibodies
    • Perform cross-validation with orthogonal methods (e.g., TEM immunogold labeling) .

  • What statistical frameworks are robust for analyzing UGT91C1 expression variability across tissues?

    • Apply mixed-effects models to account for biological replicates and technical variability.

    • Use Benjamini-Hochberg correction for multiple comparisons when assessing significance across >10 tissue types .

Methodological Insights from Recent Studies

  • How to design a CRISPR-based validation pipeline for UGT91C1 antibody specificity?

    • Step 1: Generate UGT91C1 knockout lines in Arabidopsis using SUNY Biotech’s CRISPR protocol .

    • Step 2: Compare antibody binding in wild-type vs. knockout lysates via:

      • Western blotting (reduced/no signal in knockouts)

      • Flow cytometry (shift in fluorescence intensity)

    • Efficiency metrics:

      AssayWild-Type SignalKnockout Signal
      WB57 kDa bandNo band
      Flow85% positivity<5% positivity
  • What bioinformatics tools enhance UGT91C1 epitope mapping for antibody validation?

    • Use IgBLAST to annotate antibody variable regions and predict cross-reactivity .

    • Integrate AlphaFold-predicted structures of UGT91C1 to identify surface-exposed epitopes.

Data Contradiction Analysis

  • Why do some studies report UGT91C1 involvement in flavonoid glycosylation while others do not?

    • Potential factors:

      • Genetic background: Use Arabidopsis ecotypes with sequenced genomes (e.g., Col-0 vs. Ler) .

      • Growth conditions: Standardize light intensity (e.g., 120 μmol/m²/s) and soil nitrate levels.

    • Cross-reference with RNA-seq data to confirm UGT91C1 expression correlates with flavonoid levels .

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