Resources

Proteomics Databases



Metabolomics Databases

• • Workflow of Protein Gel and Imaging Analysis

  Protein gel electrophoresis and imaging analysis are essential techniques for studying protein structure and function. This technique involves the separation, transfer, and detection of protein samples, providing insights into their molecular weight, polymorphism, and expression levels. The following sections detail the workflow of protein gel electrophoresis and imaging analysis.

• • Application of Protein Gel and Imaging Analysis

  Protein gel and imaging analysis techniques hold a pivotal role in modern biological research. These technologies not only offer efficient methods for protein separation, purification, and identification but also significantly aid in understanding protein functions, interactions, and their roles in various diseases.

• • Workflow of Protein Hydrolysis

  Protein hydrolysis is a crucial process in biological research, widely used in protein function studies, proteomics analysis, and drug development. Protein hydrolysis refers to the process of breaking down proteins into smaller peptides or amino acids through physical, chemical, or enzymatic means. This article will detail the workflow of protein hydrolysis, focusing on the specific operations and considerations at each step.

• • Advantages and Disadvantages of Protein Gel and Imaging Analysis

  Protein gel electrophoresis and image analysis are pivotal techniques in contemporary biological research. These methodologies are extensively utilized not only in foundational research but also in clinical diagnostics and drug discovery. This article aims to elucidate the advantages and disadvantages of protein gels and image analysis to assist researchers in optimizing their use of these technologies.

• • Principle of Protein Hydrolysis

  Protein hydrolysis is a crucial process in the fields of biology and biochemistry, involving the breakdown of proteins into their constituent amino acids or peptides. This process plays a key role in many biological functions, including digestion, cellular metabolism, signal transduction, and protein turnover. This article will delve into the basic principles of protein hydrolysis, the main types of hydrolytic enzymes, and its biological significance.

• • Principle of Protein Gel and Imaging Analysis

  Protein gel and imaging analysis technologies are pivotal in modern biological research. They are extensively used in protein separation and analysis, as well as in disease diagnosis, drug development, and basic research. This article provides a comprehensive overview of the fundamental principles of protein gel electrophoresis and imaging analysis, aiming to offer researchers a systematic knowledge background.

• • Application of Protein Sample Preparation

  Protein sample preparation is a critical step in biological and biochemical research, significantly impacting downstream analyses such as mass spectrometry, X-ray crystallography, and nuclear magnetic resonance (NMR). With advances in technology, methods for protein sample preparation have continually improved and refined.

• • Workflow of Protein Sample Preparation

  Protein sample preparation is a critical step in biological research. High-quality protein samples are essential for subsequent biochemical analyses, structural studies, and functional investigations. The following sections detail the workflow for protein sample preparation, including protein extraction, purification, quantification, and quality control.

• • Principle of Protein Sample Preparation

  Protein sample preparation is a critical step in biological research, directly impacting the accuracy and reliability of subsequent experiments. To obtain high-quality protein samples, scientists must adhere to a series of strict operational steps and principles. This article will detail the fundamental principles and related methods of protein sample preparation.

• • Differences of Labeled and Label-free Quantitative Proteomics

  Quantitative proteomics in proteinomics mainly involves two major strategies: labeled quantification and label-free quantification, which are used to compare protein abundance in different samples or under different treatment conditions.