At1g48610 Antibody

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Description

Gene Overview: At1g48610 in Arabidopsis thaliana

The At1g48610 gene is annotated in the Arabidopsis genome but lacks detailed functional characterization in publicly available databases. Proteomic studies involving chromatin-associated proteins and ribosomal biogenesis in Arabidopsis often highlight genes with roles in nucleic acid binding, transcriptional regulation, and RNA processing . While At1g48610 has not been directly linked to these pathways, its inclusion in antibody catalogs suggests potential involvement in cellular processes requiring precise protein detection.

Research Applications and Methodology

While direct studies using the At1g48610 Antibody are not reported in the literature, its utility aligns with established protocols for plant antibody applications:

Protein Localization and Expression Analysis

  • Western Blotting: Detects At1g48610 protein in tissue lysates or subcellular fractions.

  • Immunofluorescence: Identifies subcellular localization (e.g., nuclear, cytoplasmic) in fixed plant cells.

  • ELISA: Quantifies protein abundance in developmental or stress-response studies.

Functional Interactions

  • Co-Immunoprecipitation (Co-IP): Identifies protein complexes involving At1g48610, analogous to methods used for telomerase components in Arabidopsis .

  • Chromatin Enrichment Protocols: Potential application in profiling DNA-protein interactions, as demonstrated for histone-binding proteins .

Comparative Proteomics

  • Cross-Species Reactivity: Limited to Arabidopsis based on current data, but homologous proteins in related species (e.g., Brassica) could be explored.

  • Epitope Mapping: Uncharacterized; requires experimental validation using peptide arrays or mutagenesis .

Knowledge Gaps

  • Functional Annotation: At1g48610 lacks defined biological roles, unlike genes such as AL2 (histone binding) or MOS4 (nucleosome positioning) .

  • Antibody Specificity: No cross-reactivity data is available for non-Arabidopsis species or paralogs.

Opportunities for Innovation

  • CRISPR-Cas9 Knockouts: Combine antibody-based detection with gene-editing tools to study At1g48610 knockouts in planta.

  • Proteomic Integration: Pair with mass spectrometry to map interactomes, as done for ribosomal proteins in Arabidopsis .

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
At1g48610 antibody; T1N15.24 antibody; Putative DNA-binding protein At1g48610 antibody; AT-hook DNA-binding motif-containing protein At1g48610 antibody
Target Names
At1g48610
Uniprot No.

Target Background

Function
Demonstrates DNA binding capacity.
Database Links

KEGG: ath:AT1G48610

STRING: 3702.AT1G48610.1

UniGene: At.26193

Subcellular Location
Nucleus.

Q&A

Given the lack of specific information on "At1g48610 Antibody" in the search results, I will provide a general framework for FAQs related to antibody research, focusing on academic scenarios. This framework can be adapted to any specific antibody, including hypothetical or less-documented ones like "At1g48610 Antibody."

Data Interpretation and Contradiction Analysis

  • Q: What if my data from different experiments using At1g48610 Antibody seem contradictory?

  • A: Analyze potential sources of variation:

    • Experimental Conditions: Check for differences in buffer composition, temperature, or incubation times.

    • Sample Preparation: Ensure consistent sample handling and processing.

    • Antibody Lot Variability: Verify if different lots of the antibody were used.

Advanced Research Questions: Epitope Mapping

  • Q: How can I determine the epitope recognized by At1g48610 Antibody?

  • A: Epitope mapping can be achieved through:

    • Peptide Arrays: Test the antibody against overlapping peptides of the target protein.

    • Mutagenesis Studies: Introduce point mutations in the protein and assess antibody binding.

Methodological Considerations for Antibody Selection

  • Q: What factors should I consider when selecting an antibody for my research?

  • A: Key considerations include:

    • Specificity and Sensitivity: Choose antibodies with high specificity and sensitivity for the target protein.

    • Cross-reactivity: Check for potential cross-reactivity with other proteins.

    • Application Suitability: Ensure the antibody is suitable for the intended experimental technique (e.g., Western blot, immunofluorescence).

Troubleshooting Common Issues

  • Q: My At1g48610 Antibody is not working as expected. What are common issues to troubleshoot?

  • A: Common issues include:

    • Insufficient Antibody Concentration: Increase the antibody concentration or incubation time.

    • Incorrect Blocking Conditions: Adjust blocking agents or times to reduce non-specific binding.

    • Sample Quality: Check for degradation or contamination in samples.

Integrating Antibody Data with Other Research Findings

  • Q: How can I integrate data from antibody experiments with other research findings, such as gene expression or proteomics data?

  • A: Use bioinformatics tools to correlate antibody binding data with gene expression or proteomics data. This can help validate findings and provide a more comprehensive understanding of biological processes.

Advanced Techniques for Antibody Characterization

  • Q: What advanced techniques can I use to further characterize At1g48610 Antibody?

  • A: Consider using:

    • Mass Spectrometry: For detailed analysis of antibody-protein interactions.

    • Single-Molecule Localization Microscopy (SMLM): To study protein localization at the nanoscale.

    • Protein-Protein Interaction Assays: To investigate interactions between the target protein and other proteins.

Collaboration and Resource Sharing

  • Q: How can I collaborate with other researchers or share resources related to At1g48610 Antibody?

  • A: Utilize academic networks, attend conferences, and participate in online forums to share data and collaborate on projects. Consider depositing antibodies in public repositories to facilitate access for other researchers.

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