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相关概念视频

Size-Exclusion Chromatography01:08

Size-Exclusion Chromatography

665
In size-exclusion chromatography (SEC), also known as molecular-exclusion or gel-permeation chromatography, molecules are separated based on their sizes. This technique is important for separating large molecules such as polymers and biomolecules. The two classes of micron-sized stationary phases encountered in SEC are silica particles and cross-linked polymer resin beads. Both materials are porous, but their pore sizes vary significantly.
Silica particles offer advantages such as rigidity,...
665
Capillary Electrophoresis: Applications01:30

Capillary Electrophoresis: Applications

441
Capillary electrophoretic separations offer various modes, each with unique applications. These modes include capillary zone electrophoresis, capillary gel electrophoresis, capillary array electrophoresis, capillary isoelectric focusing, capillary isotachophoresis, micellar electrokinetic chromatography, and capillary electrochromatography.
Capillary zone electrophoresis (CZE) separates ionic components based on their electrophoretic mobility. It has been used to separate proteins, amino acids,...
441
Centrifugation01:05

Centrifugation

2.4K
Centrifugation is a separation technique based on differences in density or size. It is commonly used to separate solids from aqueous interferents. During centrifugation, the sample is placed in centrifugation tubes and spun at high angular velocity, which allows centrifugal force to act differentially on the different densities or masses of the components. After spinning, the supernatant liquid is decanted. Depending on the specific application, either the pellet or the supernatant is retained...
2.4K
Two-dimensional Gel Electrophoresis01:22

Two-dimensional Gel Electrophoresis

6.1K
Two-dimensional gel electrophoresis is a high-resolution protein separation method first introduced by O' Farrell and Klose in 1975. This method involves protein separation by two dimensions, mass and charge, making it more accurate than one-dimensional gel electrophoresis.
The first dimension separation uses the isoelectric focusing or IEF technique performed on immobilized pH gradient (IPG) strips that separate proteins according to their isoelectric points.
Biological samples, such...
6.1K
Overview Of Cell Separation And Isolation01:20

Overview Of Cell Separation And Isolation

5.8K
Cell separation was first achieved in 1964 by S. H. Seal, who separated large tumor cells from the smaller blood cells using filtration. Two years later, Pohl and Hawk performed experiments on how cells respond differently to a nonuniform electric field based on the cell type. Such observations were the inception of cell separation methods, which allow isolating a single cell type from a heterogeneous sample.
5.8K
Subcellular Fractionation01:32

Subcellular Fractionation

7.1K
The homogenate obtained after cell lysis contains various membrane-bound organelles that can be further separated into pure fractions by subcellular fractionation. These isolates are used to study specific cellular components, analyze localized protein activity, and are even employed in diagnostics. Fractionation is typically achieved using centrifugation methods, the most common being density-gradient and differential centrifugation.
Differential Centrifugation
Differential centrifugation is...
7.1K

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相关实验视频

Updated: Jul 25, 2025

Identification of Protein Complexes in Escherichia coli using Sequential Peptide Affinity Purification in Combination with Tandem Mass Spectrometry
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Identification of Protein Complexes in Escherichia coli using Sequential Peptide Affinity Purification in Combination with Tandem Mass Spectrometry

Published on: November 12, 2012

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蛋白质分离通过连续的选择性复合同化.

Jin Zhou1, Ying Cai1, Yuting Wan1

  • 1State-Key Laboratory of Chemical Engineering, and Shanghai Key Laboratory of Multiphase Materials Chemical Engineering, East China University of Science and Technology, 130 Meilong Road, 200237 Shanghai, People's Republic of China.

Journal of colloid and interface science
|June 24, 2023
PubMed
概括
此摘要是机器生成的。

这项研究引入了一种连续的联合化方法,用于净化像牛血清白蛋白 (BSA) 和马过氧化酶 (HRP) 等蛋白质. 该过程有效地分离具有不同同电点的蛋白质,提供可持续的工业解决方案.

关键词:
复杂的联合化.聚电解质是一种多电解质.蛋白质分离 蛋白质分离有选择性的复杂化.

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Resolving Affinity Purified Protein Complexes by Blue Native PAGE and Protein Correlation Profiling

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Identification of protein complexes with quantitative proteomics in S. cerevisiae
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Identification of Protein Complexes in Escherichia coli using Sequential Peptide Affinity Purification in Combination with Tandem Mass Spectrometry
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Resolving Affinity Purified Protein Complexes by Blue Native PAGE and Protein Correlation Profiling
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Identification of protein complexes with quantitative proteomics in S. cerevisiae
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科学领域:

  • 生物化学 生物化学
  • 材料科学 材料科学 材料科学
  • 化学工程是化学工程的重要组成部分.

背景情况:

  • 对特定蛋白质的有效隔离对于食品制造和生物医学应用至关重要.
  • 从自然来源净化蛋白质带来了重大挑战.
  • 现有的方法经常在选择性和可扩展性方面扎.

研究的目的:

  • 为选择性蛋白质隔离和净化开发一个连续的同化过程.
  • 为了从混合溶液中分离牛血清白蛋白 (BSA) 和马过氧化酶 (HRP).
  • 展示一个可扩展和可持续的蛋白质分离策略.

主要方法:

  • 使用了由多电解质 (聚乙烯胺和聚烯酸) 触发的序列复合协.
  • 操纵pH和离子强度以实现选择性蛋白质复合.
  • 采用相位分离来分离和净化蛋白 (BSA和HRP).

主要成果:

  • 在第一步中达到100%的马过氧化酶 (HRP) 在上游剂中达到91%的纯度.
  • 在第二步中回收了大约75%的牛血清白蛋白 (BSA),其纯度为99%.
  • 根据不同的同电点 (PI) 证明了选择性蛋白质分离.

结论:

  • 在受控条件下的顺序共使选择性蛋白质净化成为可能.
  • 开发的方法简单,可持续,并显示出工业规模蛋白质分离的潜力.
  • 这种方法为获得各种应用的纯蛋白质提供了有效的替代方案.