Haemophilus influenzae DNA lab quality control

Texnik xususiyatlari

Qadoq	Frozen vial; 10 ^ 8~10 ^ 9copies/mL;10 tubes/box
Ozuqa muhiti	Special peptone: 23.0, soluble starch: 1.0, sodium chloride: 5.0, agar: 20.0, defibrated sheep blood: 5%,pH:7.3±0.2(25 ℃)
Qo‘llash tartibi	Remove from the refrigerator, melt completely, vortex and mix well, ready to use. Note: The quality control is inactivated particles, which need to be used after nucleic acid extraction. The extraction or purification reagents should be prepared by themselves, and repeated freezing and thawing should be avoided before extraction. The minimum sampling volume is 200 μL.
O‘stirish sharoiti	37 ℃,18-24h,5% CO2 + 95% air
Saqlash sharoiti	-80 ℃
Xavfsizlik darajasi	2
Isolation	Throat of young adult with respiratory infection
Qo‘llanilishi	quality control can be used for precision testing in relevant laboratories. They can be used for indoor quality control of Haemophilus influenzae nucleic acid detection reagent manufacturers and relevant laboratories that carry out Haemophilus influenzae nucleic acid detection. They can effectively monitor the instrument status, personnel operation and kit effectiveness to ensure the accuracy and reliability of test results, but they are not used for reagent evaluation and negative and positive result judgment.