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在实时定量聚合酶链反应(RT-qPCR)检测的模拟运输环境条件下,评估[具体物质]在各种介质中的稳定性。

Evaluating the stability of in various media under simulated environmental conditions of shipment for RT-qPCR assays.

作者信息

Boggan SaraBeth, Williams Ryan B, Koziol Jennifer H

机构信息

Texas Tech School of Veterinary Medicine, Amarillo, TX, USA.

出版信息

J Vet Diagn Invest. 2025 Apr 16:10406387251330297. doi: 10.1177/10406387251330297.

Abstract

is a notable reproductive pathogen in cattle, and the processes of sample collection, handling, transportation, and testing present considerable challenges for surveillance initiatives. Advancements include the development of a direct detection method for using reverse-transcription quantitative real-time PCR. We compared the stability of samples in 3 different media: PBS, sterile saline, and lactated Ringer solution over periods of 24-120 h, with storage temperatures of 0°C, 20°C, 37°C, and 54.5°C to mimic shipping of samples in various environmental temperatures.

摘要

是牛身上一种显著的生殖病原体,样本采集、处理、运输和检测过程给监测工作带来了巨大挑战。进展包括开发了一种使用逆转录定量实时PCR的直接检测方法。我们比较了样本在3种不同培养基(磷酸盐缓冲液、无菌生理盐水和乳酸林格氏液)中在24 - 120小时内的稳定性,储存温度为0°C、20°C、37°C和54.5°C,以模拟在各种环境温度下样本的运输情况。

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