At5g49000 Antibody

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Description

Target Protein: At5g49000

The antibody targets the protein encoded by the At5g49000 locus in Arabidopsis thaliana. Key characteristics include:

  • UniProt ID: Q9FI70 .

  • Gene Function: The biological role of At5g49000 remains uncharacterized in published literature, though its presence in antibody catalogs suggests interest in its regulatory or structural functions .

Research Applications

While no peer-reviewed studies specifically using the At5g49000 antibody were identified, its potential applications include:

  • Protein Localization: Tracking subcellular distribution via immunocytochemistry .

  • Expression Profiling: Quantifying protein levels under stress conditions, akin to methods used for ASK13 in seed germination studies .

  • Interaction Studies: Identifying binding partners through techniques like yeast two-hybrid screening .

Availability and Validation

  • Commercial Sources: Available through Cusabio ($50 delivery fee) and PhytoAB .

  • Validation Status: No independent validation data or user reviews are publicly documented .

Future Directions

  • Functional Studies: Characterizing At5g49000’s role in plant development or stress responses.

  • Technical Optimization: Developing protocols for Western blotting or immunofluorescence using this antibody.

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M Phosphate Buffered Saline (PBS), pH 7.4
Form
Liquid
Lead Time
14-16 week lead time (made-to-order)
Synonyms
At5g49000 antibody; K19E20.13F-box/kelch-repeat protein At5g49000 antibody
Target Names
At5g49000
Uniprot No.

Q&A

The At5g49000 antibody is widely used in plant molecular biology research, particularly for studying Arabidopsis thaliana proteins. Below are structured FAQs addressing both foundational and advanced methodological considerations for academic researchers.

Advanced Research Challenges

Resolving tissue-specific detection discrepancies

  • Problem: Variable signal intensity in root vs. leaf extracts.

  • Solution:

    • Validate RNA expression correlation using qRT-PCR (ΔΔCt method)

    • Test protease inhibitor cocktails for tissue-specific protein degradation

    • Perform subcellular fractionation to identify localization differences

Cross-reactivity analysis with homologous proteins

  • Method:

    • BLAST alignment of antigenic peptide against Brassicaceae proteomes

    • Quantitative comparison via ELISA cross-adsorption assays

Co-immunoprecipitation experimental design

  • Critical parameters:

    • Lysis buffer composition (RIPA vs. native buffers)

    • Crosslinker choice (DSP vs. formaldehyde) for transient interactions

    • Elution conditions for MS-compatible workflows

Data Interpretation Framework

Experimental contradiction resolution:

  • Validate antibody lot consistency via parallel testing with previous batches

  • Compare results across orthogonal methods (e.g., IF vs. Western)

  • Analyze post-translational modifications using Phos-tag® gels

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