At1g11920 Antibody

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Description

Nomenclature Analysis

The identifier "At1g11920" follows Arabidopsis thaliana (a model plant species) gene nomenclature conventions, where:

  • At: Arabidopsis thaliana

  • 1g: Chromosome 1

  • 11920: Unique locus identifier

Search Result Review

The provided sources focus on antibodies targeting human receptors (e.g., angiotensin II receptor, endothelin receptor) or pathogens (e.g., HIV, SARS-CoV-2). Key findings from these sources include:

  • Antibody specificity for GPCRs like AT1R and ETAR in COVID-19 patients .

  • Structural insights into HIV-neutralizing antibodies like N6 .

  • Germline-encoded determinants of antibody homotypic interactions .

None mention Arabidopsis thaliana proteins or plant-specific antibodies.

Hypothesis 1: Typographical Error

If the intended target was AT1R (Angiotensin II Receptor Type 1), extensive data exists (e.g., ):

PropertyAnti-AT1R Antibody (AAR-011)
TargetHuman AT1R extracellular domain
ApplicationsWB, IHC, Flow Cytometry
Species ReactivityHuman, Mouse, Rat
Associated DiseasesHypertension, COVID-19

Hypothesis 2: Obscure or Proprietary Antibody

If "At1g11920 Antibody" refers to a proprietary reagent, it may not be published or cataloged in public databases.

Recommendations for Further Investigation

  1. Verify the compound name for typographical errors (e.g., AT1R vs. At1g11920).

  2. Consult Arabidopsis-centric resources:

    • TAIR (The Arabidopsis Information Resource) for gene annotations.

    • ABRC (Arabidopsis Biological Resource Center) for antibodies.

  3. Explore cross-reactivity: Plant FLAs share structural motifs with mammalian proteins, but no cross-reactive antibodies are documented in the provided sources.

Product Specs

Buffer
Preservative: 0.03% Proclin 300
Composition: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
At1g11920 antibody; F12F1.22 antibody; Putative pectate lyase 2 antibody; EC 4.2.2.2 antibody
Target Names
At1g11920
Uniprot No.

Q&A

Here’s a structured collection of FAQs tailored for researchers working with the At1g11920 Antibody in plant molecular biology, integrating experimental design principles and data analysis challenges:

Advanced Research Questions

  • How to resolve contradictions between transcriptomic and proteomic data for At1g11920 under nanoparticle stress?

    • Case study: In AuNP-SCTA-treated Arabidopsis:

      Analysis TypeFold Change (6h)Fold Change (7d)
      RNA-seq+2.1-1.8
      ProteomicsNo change-3.2
    • Resolution workflow:

      1. Verify antibody performance in stressed samples

      2. Perform ribosome profiling to assess translational efficiency

      3. Test protein degradation rates via cycloheximide chase assays

  • What multi-omics strategies best characterize At1g11920's role in cell wall remodeling?

    • Key findings: Co-regulated DEGs/DEPs in pectin catabolism pathways (e.g., PME, PG) suggest compensatory mechanisms [Fig A-1, A-3].

Technical Optimization Questions

  • How to design CRISPR mutants for functional validation of At1g11920 antibodies?

    • Guide RNA design:

      Target ExonsgRNA Sequence (5'-3')Off-Target Score
      Exon 2GACCTGCGATCAGCTCAACG94
      Exon 4TCCGATACGGCTACGTACAA88
    • Validation triad:

      • Antibody signal loss in mutants

      • Complementation assay rescue

      • Phenotypic correlation with cell wall defects

  • What statistical frameworks are robust for time-series analysis of At1g11920 expression?

    • Recommended models:

      • Linear mixed-effects models for longitudinal data

      • Gaussian processes for irregular sampling intervals

    • Case application: Analysis of oxidative burst kinetics (FOX assay) showed time-dependent antibody signal attenuation (p < 0.01, ANOVA) [2.2.7.4].

Data Interpretation Challenges

  • How to distinguish between direct antibody recognition artifacts and true biological variation?

    • Control matrix:

      ConditionWT SignalMutant SignalInterpretation
      Standard IHC+++-Valid
      Heat-denatured++-Partial epitope loss
      Cross-linker treated++++-Improved antigen retrieval
    • Advanced validation: Phos-tag blotting to detect phosphorylation-state dependency .

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