RPL6C Antibody

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Product Specs

Buffer
**Preservative:** 0.03% Proclin 300
**Constituents:** 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
Made-to-order (14-16 weeks)
Synonyms
RPL6C antibody; At1g74050 antibody; F2P9.8 antibody; 60S ribosomal protein L6-3 antibody
Target Names
RPL6C
Uniprot No.

Q&A

The RPL6 antibody (often referenced in research contexts, though "RPL6C" may refer to a specific isoform or be a nomenclature variant) is a critical tool for studying ribosomal biology and cancer mechanisms. Below are FAQs structured for academic research applications, incorporating methodological guidance and evidence-based answers:

Advanced Research Questions

How to resolve contradictions in RPL6 expression data across studies?

  • Context-dependent expression: RPL6 levels vary by cell type (e.g., upregulated in drug-resistant gastric cancer vs. suppressed in gallbladder cancer) .

  • Post-translational modifications: Perform phosphatase/kinase treatments to assess phosphorylation-driven mobility shifts in Western blots.

  • Epitope mapping: Use truncated RPL6 constructs to identify antibody-binding regions (linear vs. conformational epitopes) .

What strategies integrate RPL6 antibody data with multi-omics workflows?

  • Proteomics: Combine immunoprecipitation (IP) with mass spectrometry to identify RPL6 interactors (e.g., histone H2A, NSUN2) .

  • Transcriptomics: Correlate RPL6 protein levels with ribosome profiling data to assess translational regulation.

  • CRISPR screens: Use antibody-based validation of RPL6 knockout phenotypes in genome-wide functional studies.

How to design in vivo studies targeting RPL6?

  • Xenograft models: Inject RPL6-overexpressing cancer cells into immunodeficient mice and monitor tumor growth with/without antibody treatment .

  • Tissue-specific delivery: Use lipid nanoparticles to deliver RPL6-targeting antibodies to hepatic or gallbladder tissues .

  • Pharmacodynamic endpoints: Measure downstream markers (e.g., p-STAT3, SAA) to assess RPL6 pathway modulation .

Methodological Considerations Table

TechniqueApplicationKey Considerations
Western BlotSpecificity validationInclude Jurkat lysate positive control; optimize blocking buffers to reduce background .
IHCTissue localizationAntigen retrieval critical for FFPE; validate with RNAscope for mRNA co-localization .
IP-MSInteraction mappingUse crosslinkers (e.g., DSP) to capture transient interactions; confirm with reciprocal IP .
Competition ELISAEpitope characterizationCompare binding with/without pre-incubation with recombinant protein .

Data Interpretation Challenges

  • Cross-reactivity: RB6-8C5 (anti-Ly-6G/Ly-6C) demonstrates how antibodies may bind homologous targets; apply peptide blocking for RPL6 studies .

  • Functional redundancy: In DNA damage models, use PARP inhibitors to dissect RPL6’s role vs. other repair proteins .

  • Antibody lot variability: Include a reference lysate in all experiments to normalize batch effects .

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