At1g15480 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
At1g15480 antibody; F9L1.43Pentatricopeptide repeat-containing protein At1g15480 antibody; mitochondrial antibody
Target Names
At1g15480
Uniprot No.

Target Background

Database Links

KEGG: ath:AT1G15480

STRING: 3702.AT1G15480.1

UniGene: At.41932

Protein Families
PPR family, P subfamily
Subcellular Location
Mitochondrion.

Q&A

FAQs for Researchers on AT1R (AT1g15480) Antibody in Academic Research
(Note: "AT1g15480" is assumed to refer to angiotensin receptor type 1 [AT1R] based on contextual alignment with provided literature. Adjust nomenclature as needed for specific organisms.)

Advanced Research Questions

  • How do AT1R autoantibodies contribute to disease pathogenesis at a molecular level?

    • Key mechanisms:

      • Receptor activation: AT1R antibodies enhance angiotensin II-mediated signaling via conformational changes, measured by dynamic mass redistribution (DMR) in HEK293 cells .

      • Immune cell crosstalk: Antibody-bound AT1R activates monocytes, inducing profibrotic markers (e.g., TGFβ) in dermal fibroblasts .

    • Contradiction resolution: Conflicting reports on protective vs. pathogenic roles (e.g., COVID-19 outcomes in ) may arise from:

      • Titer thresholds: Use quantitative ELISA with standardized positivity cutoffs (≥10 U/mL in ).

      • Epitope heterogeneity: Map antigenic regions via PhIP-Seq or peptide arrays (e.g., residues 149–172 in ).

  • What computational tools enable rational design of anti-AT1R antibodies?

    • Framework:

      • RosettaAntibodyDesign (RAbD): Optimize interface energy and structural stability by grafting CDR loops from canonical clusters (e.g., CYP11A1/SOX10 antigenic regions in ).

      • Risk mitigation: Calculate the design risk ratio (DRR) to prioritize native-like CDR conformations .

Data Integration Table

Research GoalMethodKey ParametersSource Example
Epitope mappingPhIP-Seq≥10-fold IP enrichment vs. mock controlsAPS1 autoantigens
Functional validationDMR technologyReal-time mass redistribution kineticsHEK293-AT1R activation
Pathogenicity assessmentHistology/IHCPerivascular inflammation scoring (0–4)Skin/lung sections
Therapeutic profilingC. elegans AD modelsAβ40 oligomer toxicity reduction (%)DesAb 18-24 efficacy

Methodological Pitfalls & Solutions

  • Low-affinity antibodies: Use high-avidity formats (e.g., IgG3) or yeast display libraries to enhance binding .

  • Non-specific aggregation: Pre-clear sera with protein A/G beads and include 0.1% Tween-20 in buffers .

  • Species cross-reactivity: Validate antibody binding across human, murine, and rat AT1R orthologs via SPR .

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