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Acid detection virus sampling tube automatic production line introduction about the use of virus sampling tube

Release Date:2022-11-07 11:24:11 Popularity:

  GST acid detection virus sampling tube filling and capping packaging automatic production line equipment manufacturers introduce the use of virus sampling tubes!

Acid detection virus sampling tube automatic production line introduction about the use of virus sampling tube

  Sampling using virus sampling tubes is mainly divided into oropharyngeal sampling and nasopharyngeal sampling:

  1. Oropharyngeal sampling: first press the tongue with a tongue depressor, then insert the head of the sampling swab into the throat to wipe the bilateral pharyngeal tonsils and posterior pharyngeal wall, and wipe the posterior pharyngeal wall with mild force, avoiding touching the tongue department.

  2. Nasopharyngeal sampling: measure the distance from the tip of the nose to the earlobe with a swab and mark it with your fingers, insert the sampling swab into the nasal cavity in the direction perpendicular to the nose (face), and the swab should be inserted at least half the length from the earlobe to the tip of the nose. Leave the swab in the nose for 15-30 seconds, swirl gently 3-5 times, and withdraw the swab.

Acid detection virus sampling tube automatic production line introduction about the use of virus sampling tube

  It is not difficult to see from the method of use, whether it is an oropharyngeal swab or a nasopharyngeal swab, sampling is a technical task, which is difficult and easy to contaminate. The quality of the collected samples is directly related to the subsequent testing. If the viral load of the collected samples Low, easy to cause false negatives, difficult to diagnose.

  Most of the samples recommended by the kits currently on the market are oropharyngeal swabs or nasopharyngeal swabs and bronchoalveolar lavage fluid. This can greatly reduce the difficulty of the samplers' work. After all, it is not difficult to collect venous blood samples, and like the detection of hepatitis C RNA, about 5 ml of EDTA anticoagulated blood samples are separated into plasma, and the extracted and purified RNA can fully meet the needs of PCR detection.


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