Resources

Proteomics Databases



Metabolomics Databases

• • DLS (Dynamic Light Scattering) Analysis of Antibody Drugs

  Antibody drugs are a class of drugs that treat diseases through artificially synthesized antibodies, such as monoclonal antibodies, artificially synthesized antibody fragments, immunotoxins, antibody drug conjugates, etc. They bind specifically with target molecules to achieve therapeutic purposes. Antibody drugs have shown significant therapeutic effects in many disease treatments, such as cancer, autoimmune diseases, inflammatory diseases, immune regulation, and ophthalmic diseases.

• • Circular Dichroism Detection of Recombinant Protein Drugs

  Recombinant protein drugs are protein therapeutic drugs produced using DNA recombination technology or other biotechnologies. They include cytokines, polypeptide hormones, recombinant enzymes, monoclonal antibodies, fusion proteins, etc. Compared with traditional low-molecular synthetic drugs, recombinant protein drugs have the advantages of high specificity, low toxicity, and significant therapeutic effects.

• • Analysis of Peptide Drugs: HCP and HCD

  Peptide drugs are bioactive molecules made up of multiple amino acids linked by peptide bonds. Typically, it consists of 10 to 100 amino acids and has a relative molecular mass below 10,000. Most peptide drugs are derived from endogenous peptides or natural peptides, so they have little or no side effects on the human body. Compared to protein drugs, peptide drugs also have advantages such as good stability, high purity, low production cost, and low immunogenicity.

• • Protein Gel Mass Spec: Pros and Cons of Sample Submission

  Proteins are significant functional molecules in organisms, and the study of their structure and function is crucial for understanding life activities. Proteomic analysis is a common technique that can provide information about the structure and composition of proteins. In proteomic analysis, protein gel strip samples are one of the commonly used sample types. This article will focus on the submission methods for proteomic analysis of protein gel strip samples, exploring their pros and cons.

• • What is the Primary Structure of a Protein?

  The primary structure of a protein refers to the linear arrangement of amino acids in the protein. In other words, it is the structure formed by connecting the individual amino acids in a specific order in the protein. Proteins are composed of 20 different amino acids, each with its unique side chain. These amino acids are connected by peptide bonds to form a peptide chain.

• • Protein Amino Acid Sequence Determination

  The determination of the amino acid sequence of a protein is referred to as protein sequence determination. Here is a basic introduction to amino acid sequence determination.

• • Analysis of Protein Sequencing Data Types

  Protein sequencing typically refers to determining the amino acid sequence of a protein. This involves sorting the amino acids of a protein to determine their exact order within the protein.

• • Application of Label Transfer in Protein Interaction Studies

  The core mechanism of the label transfer technique involves using specific labeling reagents to link a target protein with interacting proteins, thereby enabling precise protein interaction analysis. 

• • Workflow of Label Transfer Protein Interaction Analysis

  The core mechanism of the label transfer method involves treating bait proteins with labeling reagents, followed by crosslinking these reagents to prey proteins through light exposure or other activation methods. The detailed steps are as follows:

• • Advantages and Disadvantages of Label Transfer in Protein Interaction

  In protein interaction studies, the label transfer method, combined with crosslinking techniques, provides an effective means of marking proteins that interact with target proteins. This technique not only facilitates the discovery of new interactions but also validates proteins identified by other methods and analyzes protein complexes.