Resources

Proteomics Databases



Metabolomics Databases

• • Following Up on Proteins Identified by Mass Spectrometry

  For differentially expressed proteins identified by mass spectrometry, the following steps are generally involved in subsequent studies: 1. Identification and validation of target proteins: Differentially expressed proteins identified by mass spectrometry form a relatively broad protein collection, which may include various differentially expressed proteins. Therefore, the first step is to determine the target proteins for study.

• • Quantitative Proteomic Study of Yeast Phosphorylation

  Yeast, as a model organism in biological research, has always played an important role in fields such as genetics, biochemistry, and cell biology. Its simple genome structure and abundant genetic resources make it an excellent research subject for functional gene identification, metabolic regulation, and signal transduction. In this context, quantitative phosphoproteomics studies provide a powerful tool for exploring the function and regulatory mechanisms of phosphorylated proteins in yeast.

• • Plant Anther DIA Quantitative Proteomics

  Pollen, as a crucial component of the plant reproductive system, plays an important role in the formation and release of pollen grains. Behind this complex biological process, there is a series of protein interactions and regulatory mechanisms. DIA (Data Independent Acquisition) quantitative proteomics, as an advanced proteomics technology, provides us with an important tool to explore the proteome of pollen.

• • Nasopharyngeal Carcinoma Tissue Exosomal Lipidomics

  In the field of cancer research, nasopharyngeal carcinoma has always been a challenging topic. MtoZ Biolabs is committed to applying innovative lipidomics techniques to explore the lipid composition of extracellular vesicles in nasopharyngeal carcinoma tissues, in order to provide new insights and treatment strategies for this difficult medical problem.

• • Eggshell Protein Glycosylation Sites and Sugar Type Analysis

  When we cook an egg as breakfast every morning, few people would think about the scientific mysteries hidden behind this seemingly ordinary food. In fact, the glycosylation sites and glycan types inside the eggshell protein provide us with a unique window to explore biology and food science.

• • Analysis of Metal Content in Nannochloropsis

  Nannochloropsis, a type of tiny green algae, is renowned for its highly efficient photosynthesis and strong adaptability to the environment. It has attracted widespread attention in recent years in the fields of environmental ecology, bioenergy, food industry, and bioremediation.

• • Quantitative Proteomic Study of Human Cell Phosphorylation

  MtoZ Biolabs utilizes advanced mass spectrometry technology and bioinformatics analysis to perform quantitative analysis of phosphorylated proteins in human cells, revealing their crucial roles in cell signaling, disease development, and drug mechanisms of action. This research provides deep insights into cellular physiology and pathology, promoting advancements in disease diagnosis, treatment strategies, and new drug development.

• • Protein Secondary Structure Analysis of Escherichia Coli

  Secondary Structure Analysis of Escherichia coli Proteins - Sample + Technical Promotion from MtoZ Biolabs The secondary structure of Escherichia coli proteins is formed by the local interactions of amino acid sequences, primarily including α-helices, β-sheets, and β-turns. It provides crucial information for understanding the biological function of proteins. Changes in protein secondary structure may affect the stability and functionality of proteins.

• • Identification of Single Protein Modifications

  In biological research, the identification of protein modifications is an important method that helps us understand the function and characteristics of proteins. This article will focus on the research progress in the identification of single protein modifications.

• • 5X Bradford Method for Protein Concentration Measurement

  The Bradford method is a fast, convenient, and sensitive method for protein concentration determination, widely used in biochemical and molecular biology research. This method relies on the principle that the Coomassie Brilliant Blue G-250 dye changes color when it binds to proteins under acidic conditions. The higher the protein concentration, the darker the color of the sample, and the protein concentration is estimated by measuring the absorbance.