相关实验视频

Updated: Jul 12, 2025

PCR Mutagenesis, Cloning, Expression, Fast Protein Purification Protocols and Crystallization of the Wild Type and Mutant Forms of Tryptophan Synthase
09:31

PCR Mutagenesis, Cloning, Expression, Fast Protein Purification Protocols and Crystallization of the Wild Type and Mutant Forms of Tryptophan Synthase

Published on: September 26, 2020

4.4K

长度结构功能分析分子确认的CYP4V2比埃蒂晶变异

Riccardo Cheloni1,2, Neil Clough2, Daniel Jackson1,2

  • 1UCL Institute of Ophthalmology, London, EC1V 9EL, UK.

Eye (London, England)
|October 29, 2023
PubMed
概括

贝蒂晶状缩症 (BCD) 是一种遗传性视网膜疾病,进展缓慢,在60岁时有显著的视力丧失. 圆形区域 (EZ) 和胸膜的光学连贯性断层扫描 (OCT) 测量显示出快速退化,并且可能比视敏度更好的试验结果.

更多相关视频

Optimized Negative Staining: a High-throughput Protocol for Examining Small and Asymmetric Protein Structure by Electron Microscopy09:37

Optimized Negative Staining: a High-throughput Protocol for Examining Small and Asymmetric Protein Structure by Electron Microscopy

Published on: August 15, 2014

43.7K
Expression and Purification of Mammalian Bestrophin Ion Channels08:12

Expression and Purification of Mammalian Bestrophin Ion Channels

Published on: August 2, 2018

8.4K

相关概念视频

Cystic Fibrosis: Pathogenesis01:23

Cystic Fibrosis: Pathogenesis

Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
256