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    Resources

      Proteomics Databases

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      Metabolomics Databases

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    • • Protein Primary Structure Determination

      Protein structures can be divided into four levels: primary, secondary, tertiary, and quaternary structure. The primary structure of a protein refers to the linear sequence composed of amino acids. Each amino acid is connected by a peptide bond to form a polypeptide chain. The primary structure of a protein determines the formation of its secondary, tertiary, and quaternary structures, which in turn determines the functions and interactions of the protein.

    • • Protein Ubiquitination Sites Identification by Mass Spectrometry

      Ubiquitination modification is an important post-transcriptional modification of proteins in living organisms, with profound effects on many physiological processes such as gene expression, cell cycle regulation, and immune responses. However, the accurate identification of ubiquitination sites and their specific biological significance is one of the frontier challenges in the field of biopharmaceuticals.

    • • Quantitative Proteomics in Cancer Research

      Cancer, as a serious disease, significantly affects human health and quality of life. Early diagnosis and effective treatment of cancer are crucial for improving patient survival rates. In recent years, quantitative proteomics, as a powerful technique, has played an important role in cancer research. We will explore the use of quantitative proteomics in cancer research, focusing on its potential to identify biomarkers and therapeutic targets.

    • • Comprehensive Analysis of Protein-Protein Interaction Verification Methods

      MtoZ Biolabs is your optimum choice for protein-protein interactions services, with high-quality and efficient solutions.   Proteins are among the most significant molecules in living organisms, playing various key roles within cells and controlling physiological processes within the organism. Furthermore, interactions between proteins, also known as protein-protein interactions, form the basis of cellular function networks.

    • • Analyze the Dynamic Changes of Histone Modifications Using Mass Spectrometry

      Histone modification is an important regulatory mechanism in cells, affecting gene expression by altering the structure and function of chromatin. Recent developments in mass spectrometry technology have allowed us to further investigate the dynamic changes in histone modification.

    • • Protein Translation and Post-Translational Modification Detection Methods

      Post-translational modifications (PTMs) are key biochemical processes in cells that modify the chemical properties, structure, function, and location of proteins. Common post-modification of proteins includes phosphorylation, acetylation, ubiquitination, glycosylation, pantothenylation, etc. Detecting these modifications is crucial for understanding the role and regulatory mechanisms of proteins. Below are the commonly used methods to detect protein post-translational modifications:

    • • Profiling Cell Surface Proteins by Orbitrap Mass Spectrometry

      Cell surface proteins hold a crucial position in life sciences, being key players in processes such as cell signaling, substance transport, immune response, cell recognition, and pathological processes. Understanding and characterizing the expression profiles of cell surface proteins is vital for elucidating cell functions and disease mechanisms.

    • • Quantitative Analysis of Cell Surface Proteins in Cancer Research

      Cancer research is a crucial area in modern biomedical science. Cell surface proteins play a key role in the onset, progression, and metastasis of cancer, serving as important molecular markers for cancer diagnosis, prognosis assessment, and targeted therapy. Therefore, the quantitative analysis of cell surface proteins in cancer cells is of great significance.

    • • Procedure for Enriching Cell Surface Proteins Using Biotin Affinity

      Cell surface proteins play critical roles in cellular interactions with the external environment, participating in signal transduction, transport, and cell recognition. Studying these proteins is not only essential for understanding fundamental cell biology but also has applications in drug development, disease diagnosis, and therapy.

    • • Quantitative Analysis of Peptides Using Parallel Reaction Monitoring

      In proteomics research, precise quantification of proteins is crucial for uncovering the molecular mechanisms underlying biological processes. Traditional protein quantification methods include isotope labeling techniques (e.g., SILAC, iTRAQ) and label-free quantification methods (e.g., DIA).

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