- Primary Structure Analysis
- High-resolution mass spectrometry molecular weight
- MALDI TOF mass spectrometry analysis
- N-terminal sequence analysis
- C-terminal sequence analysis
- N/C terminal sequence analysis
- Analysis of the K deletion ratio at the C-terminus of antibodies
- LC-MS/MS protein full sequence validation
- Peptide coverage / Peptide spectrum analysis
- Protein peptide profile determination
- Amino Acid Composition Analysis
- Extinction coefficient analysis
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- Advanced Structural Analysis
- Charge Heterogeneity Analysis
- Impurity Analysis
- Native Mass Spectrometry
- SDS-PAGE protein purity analysis
- Protein purity analysis (size exclusion/reverse phase chromatography)
- Host Cell Protein Residue (HCP) Analysis Service
- Antibody-Drug Conjugates (ADCs) Analysis
- Protein content analysis
- Product-related impurity analysis
- Analysis of other process-related impurities
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- Special Analysis
- Primary Structure Analysis
Aptamer-Based Proteomics
Aptamer-based proteomics refers to the use of nucleic acid aptamers to specifically recognize and bind to target proteins, thereby enabling qualitative and quantitative analysis of proteins. These nucleic acid aptamers are composed of nucleic acid sequences (such as DNA or RNA) and are selected from a large sequence library through in vitro selection technology (SELEX) for molecules with high affinity and specificity for specific proteins. Compared to traditional antibody detection technologies, aptamer-based proteomics shows significant advantages in specificity, stability, cost, and scalability. This technology is widely used in early disease diagnosis, biomarker discovery, drug target identification, and personalized medicine. In fields such as oncology, immune diseases, and neurodegenerative diseases, aptamer-based proteomics provides strong support for the analysis of disease molecular mechanisms and the optimization of treatment plans. With the development of technology and the expansion of application scenarios, aptamer-based proteomics is gradually becoming an integral part of proteomics research.
1. Common Methods of Aptamer-based Proteomics
1. SELEX Technology
SELEX (Systematic Evolution of Ligands by EXponential enrichment) is the core technology of aptamer-based proteomics. It involves multiple rounds of selection to pick nucleic acid aptamers with high affinity and specificity for the target protein from a random nucleic acid library.
2. High-throughput Detection Platforms
Using high-throughput nucleic acid chips or liquid chromatography-mass spectrometry (LC-MS) technology, interactions between nucleic acid aptamers and target proteins are detected on a large scale to achieve qualitative and quantitative analysis of proteins.
3. Fluorescent Labeling Method
By introducing fluorescent labels onto nucleic acid aptamers, real-time monitoring and quantification of proteins are achieved, particularly suitable for rapid screening of complex samples.
2. Technical Process
1. Target Protein Selection
Select target proteins based on research objectives, usually biomarkers, drug targets, or disease-related proteins.
2. Aptamer Selection
Conduct in vitro screening of nucleic acid aptamers using SELEX technology to ensure high affinity and specificity for target proteins.
3. Aptamer Modification and Optimization
Chemically modify the selected aptamers to enhance their stability and binding efficiency, adapting them to different experimental environments.
4. Proteomics Detection
Utilize aptamers to bind with target proteins in samples for high-throughput screening and data collection.
5. Data Analysis
Analyze proteomics data using bioinformatics tools to identify key proteins and their functional networks.
3. Advantages of Aptamer-based Proteomics Technology
1. High Specificity and Affinity
Aptamers can specifically bind to target proteins, reducing non-specific background noise.
2. Strong Stability
Aptamers exhibit good stability under varying environmental conditions such as temperature and pH, suitable for different sample conditions.
3. Cost-effectiveness
Compared to antibody preparation, the synthesis and selection of aptamers are less costly and have shorter production cycles.
4. Reproducibility
Nucleic acid aptamers have high consistency during synthesis, ensuring reproducibility of experimental results.
5. High Scalability
The sequence design and modification of aptamers are flexible, allowing specific recognition of different proteins.
With profound technical expertise and an experienced research team, Beritac Biotech provides professional aptamer-based proteomics services. Our services cover the entire process of aptamer selection, sample processing, protein identification, and data analysis, ensuring high-quality and accurate proteomics data. Whether in disease biomarker research, drug target discovery, or personalized medicine, Beritac is committed to providing efficient and precise solutions for clients. We look forward to closely collaborating with research partners to promote continuous innovation and development in the life sciences field.
Beritac Biotech - A Leading Provider of Biopharmaceutical Characterization and Multi-omics Mass Spectrometry Analysis Services
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