At1g69290 Antibody

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Description

Definition and Target Protein

At1g69290 antibody is an immunological reagent targeting the pentatricopeptide repeat-containing protein At1g69290 in Arabidopsis thaliana. This protein, encoded by the gene At1g69290, belongs to the pentatricopeptide repeat (PPR) superfamily, which is involved in RNA binding, editing, and processing in plant organelles . The protein comprises 658 amino acids and contains conserved PPR motifs critical for its role in mitochondrial or plastid RNA metabolism .

Antigenic Regions

The antibody is generated against synthetic peptides representing specific regions of the protein:

  • N-terminus: Amino acids 1–30

  • C-terminus: Amino acids 629–658

  • Mid-region (M): Non-terminal sequences .

Antibody Types

TypeHost SpeciesClonalityApplications
Monoclonal (X-P0C7R4)MouseCombination mAbsELISA, Western Blot (WB)
PolyclonalRabbitAntigen-affinityWB, Immunoprecipitation (IP)

Monoclonal antibodies from Abmart are provided as combinations (e.g., X-P0C7R4-N for N-terminus targeting) with ELISA titers of 10,000 and WB detection limits of ~1 ng .

Subcellular Localization

Studies using fluorescent tagging and mass spectrometry confirm that At1g69290 localizes to mitochondria or plastids, consistent with its role in organellar RNA processing .

Study ModelLocalization PredictionExperimental Confirmation
ArabidopsisMitochondria/PlastidFluorescent signal (M/C)
Transfected COS-7N/AMitochondrial targeting

Biological Role

At1g69290 participates in:

  • RNA editing (e.g., rpoB, ndhB in plastids) .

  • Stabilization of organellar transcripts critical for plant development .

Key Products

SupplierProduct CodeTypePrice (USD)Applications
AbmartX-P0C7R4-NMonoclonal$599ELISA, WB
MyBioSourceMBS7150860PolyclonalUndisclosedWB, ELISA, IP

Experimental Validation

  • Western Blot: Detects ~75 kDa band in Arabidopsis extracts .

  • ELISA: High specificity with no cross-reactivity reported .

Applications in Plant Biology

  1. Functional Studies: Elucidating RNA metabolism mechanisms in plant organelles .

  2. Diagnostic Tools: Used in Western blotting to validate CRISPR-edited Arabidopsis lines .

  3. Protein Interaction Mapping: Identifies binding partners via immunoprecipitation .

Challenges and Future Directions

  • Epitope Specificity: Further validation required to distinguish between isoforms .

  • In Vivo Function: Limited data on knockout phenotypes; CRISPR-based studies are ongoing .

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
At1g69290 antibody; F23O10.12 antibody; F23O10.28 antibody; Pentatricopeptide repeat-containing protein At1g69290 antibody
Target Names
At1g69290
Uniprot No.

Q&A

Based on a comprehensive analysis of available research literature, here is a structured FAQ addressing key technical and methodological aspects of working with At1g69290 antibody in plant molecular biology research. While no direct references to At1g69290 antibody were found in the examined literature, these questions are framed using established antibody development and validation methodologies from related studies.

Advanced Research Questions

How to resolve contradictory ChIP-seq vs Y1H data for At1g69290 binding targets?

Conflict Resolution Workflow:

  • Technical audit:

    • Verify antibody batch consistency (historical lot data)

    • Re-analyze raw sequencing data with updated genome annotation

  • Biological context analysis:

    • Compare growth conditions (light/temp differences between studies)

    • Test dimerization partners through co-IP/MS

  • Functional validation:

    • CRISPR-Cas9 editing of disputed binding sites

    • Luciferase reporter assays with mutated cis-elements

Approach adapted from TF target validation in and antibody characterization in

How to establish species cross-reactivity while maintaining specificity?

Develop a decision matrix:

Test SpeciesExpected Cross-ReactivityValidation Assay
Arabidopsis (Col-0)100% (positive control)Western blot
Arabidopsis (Ler)≥90%ELISA
Brassica napus50-70%Immunofluorescence
Oryza sativa≤10%SPR kinetics

Design principle from multi-species validation in and

What statistical approaches handle batch effects in long-term studies?

Implement mixed-effects model:

yij=μ+αi+βj+ϵijy_{ij} = \mu + \alpha_i + \beta_j + \epsilon_{ij}
Where:

  • αi\alpha_i: Antibody lot fixed effect

  • βj\beta_j: Experimental batch random effect

  • ϵij\epsilon_{ij}: Measurement error

Critical validation steps:

  • ANOVA with Tukey post-hoc for lot comparisons

  • PCA of raw fluorescence intensities

  • Standard curve parallelism testing

Statistical framework adapted from and

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