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基于毛细管的 MYO7A 免疫印迹优化

Optimization of Capillary-Based Western Blotting for MYO7A.

机构信息

Department of Pediatrics, University of Florida, Gainesville, FL, USA.

出版信息

Adv Exp Med Biol. 2023;1415:125-130. doi: 10.1007/978-3-031-27681-1_19.

Abstract

Myosin VIIA (MYO7A)-associated Usher syndrome type 1B (USH1B) is a severe disorder that impacts the auditory, vestibular, and visual systems of affected patients. Due to the large size (~7.5 kb) of the MYO7A coding sequence, we have designed a dual adeno-associated virus (AAV) vector-based approach for the treatment of USH1B-related vision loss. Due to the added complexity of dual-AAV gene therapy, careful attention must be paid to the protein products expressed following vector recombination. In order to improve the sensitivity and quantifiability of our immunoassays, we adapted our traditional western blot protocol for use with the Jess™ Simple Western System. Following several rounds of testing, we optimized our protocol for the detection of MYO7A in two of our most frequently used sample types, mouse eyes, and infected HEK293 cell lysates.

摘要

肌球蛋白 VIIA(MYO7A)相关的 Usher 综合征 1B 型(USH1B)是一种严重的疾病,会影响受影响患者的听觉、前庭和视觉系统。由于 MYO7A 编码序列的大小较大(约 7.5 kb),我们设计了一种基于双腺相关病毒(AAV)载体的方法来治疗 USH1B 相关的视力丧失。由于双 AAV 基因治疗的复杂性增加,必须仔细注意载体重组后表达的蛋白质产物。为了提高我们免疫测定的灵敏度和可量化性,我们对传统的 Western blot 方案进行了改编,以适应 Jess™ Simple Western 系统的使用。经过几轮测试,我们优化了我们的方案,用于检测我们最常使用的两种样本类型中的 MYO7A,即小鼠眼睛和感染的 HEK293 细胞裂解物。

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