Resources
Proteomics Databases

Metabolomics Databases

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• Antibody Drug Excipient Detection
As a class of therapeutic biological products, antibody drugs require precise biotechnology techniques and rely on various raw materials to support drug production and stability. These raw materials include but are not limited to amino acids, carbohydrates, protein stabilizers, buffers, surfactants, etc., which play an essential role in ensuring the efficiency of cell culture processes, the purity of antibody drugs, and the quality of the final formulation.
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• Antibody Drug Ultraviolet Spectrum Analysis
Antibody drugs, as a breakthrough in biotechnology, are now widely used in the treatment of various diseases, including cancer, autoimmune diseases, and infectious diseases. These drugs are usually precisely designed protein molecules that can specifically bind to targets in the human body, such as specific molecules on pathogens or diseased cells, thereby guiding the attack of the immune system or directly blocking the pathological process.
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Secreted proteins refer to proteins that are synthesized by cells and secreted into the extracellular space. They play important roles in various biological processes, such as signal transduction, intercellular communication, immune response, and hormone secretion. These proteins are usually synthesized in the endoplasmic reticulum (ER) of cells and then transported to the extracellular space through a series of biosynthesis and transport processes.
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• Untargeted Proteomics Sequencing
Untargeted Proteomics Sequencing aims to comprehensively analyze all proteins in a biological sample, rather than focusing on specific proteins. It helps study the complexity of the proteome and discover new protein biomarkers. Protein sequencing is the process of determining the amino acid sequence of a protein.
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• Proteomic Screening for Differential Proteins
Proteomics is a method for studying the composition and function of all proteins expressed in an organism. Screening for differentially expressed proteins is one of the important tasks in proteomics research, as it helps researchers identify proteins that show changes in expression levels under different conditions or in different tissues, thus providing insights into biological processes and disease mechanisms within organisms.
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• How to Detect the Level of Histone Methylation?
Histone methylation refers to the process of adding methyl groups to specific lysine (Lys) and arginine (Arg) residues on histone proteins. This is a common epigenetic modification that has significant effects on chromatin structure and gene expression regulation. Detecting the level of histone methylation is one of the fundamental techniques in the study of epigenetics. Here are some commonly used detection methods:
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Label-free proteome typically refers to a group of proteins in proteomics research that does not rely on any form of chemical or isotopic labeling for protein quantification analysis. Their analysis and quantification depend on label-free techniques, such as mass spectrometry-based relative quantification analysis.
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Plasma proteomics is an emerging scientific field that aims to analyze and understand the protein composition and function in plasma. Plasma, as one of the most abundant biological fluids in the human body, contains thousands of proteins that reflect the body's health status, disease processes, and treatment responses. Therefore, plasma proteomics holds great potential for disease diagnosis, treatment, and prognosis assessment.
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• DIA Data Analysis Methods in Proteomics
Data-Independent Acquisition (DIA) is a mass spectrometry technique used for high-throughput, deep analysis of the proteome in complex biological samples. Compared to the traditional Data-Dependent Acquisition (DDA) method, DIA provides a more comprehensive and reproducible proteome analysis.
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• Application and Analysis of TMT Technology in Proteomics
TMT (Tandem Mass Tags) technology is an advanced method used for protein quantification analysis in proteomics research. TMT labeling involves the use of a series of chemically distinct tags with different weights that can be attached to the amino terminus and side chains of peptides. This allows for simultaneous processing of multiple samples which are then combined for mass spectrometry analysis.
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