Reagent kit for synchronously detecting hepatitis, AIDS virus and syphilis helicoid nucleic acid
A technology for Treponema pallidum and HIV, applied in biochemical equipment and methods, and microbial measurement/inspection, etc., can solve problems such as lack of promotion and popularization, impact on blood safety, lack of simultaneous quantitative detection technology and products for four kinds of pathogenic nucleic acids , to achieve the effect of excellent specificity and excellent sensitivity
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Embodiment 1
[0059] One, embodiment 1: kit composition and preparation
[0060] 1. Synchronous extraction of pathogen concentrate and DNA and RNA
[0061] For self-preparation, pathogen concentrate: 20% PEG6000 volume fraction in normal saline solution. DNA and RNA synchronous extraction solution: the final concentration is 4mol / L guanidine isothiocyanate, the volume fraction is 0.5% sodium lauryl sarcosinate, 0.1mmol / L β-mercaptoethanol, 25mmol / L sodium citrate, 0.20g / L glycogen.
[0062] 2. Fluorescent PCR reaction solution
[0063] .20.0mmol / L MgSO 4 The 10×buffer, the forward and reverse primers of hepatitis B virus, hepatitis C virus, HIV and Treponema pallidum are 10 μmol / L respectively, and the fluorescent probes of hepatitis B virus, hepatitis C virus, HIV and Treponema pallidum are respectively is 10μmol / L, 25mmol / L
[0064] MgCl 2 , 10mmol / L dNTPs mix and sterile double distilled water.
[0065] 3. Standard positive template storage solution
[0066] Concentration is 10 ...
Embodiment 2
[0068] 2. Example 2: Synchronous detection of hepatitis B, hepatitis C, HIV and Treponema pallidum using kits
[0069] 1. Put 100 μl of body fluid specimen into a 1.5ml centrifuge tube, add an equal volume of pathogen concentrate, shake well, centrifuge at 10,000 g for 15 minutes, add 50 μl of DNA and RNA synchronous extraction solution to the precipitate, mix well, and place at 37°C or room temperature for 15 minutes; Then add 100ul-20°C pre-cooled isopropanol, precipitate at 4°C for 15min, centrifuge at 10,000g for 15min, discard the supernatant; add 500ul of 75% ethanol to the precipitate, invert several times to wash the remaining isopropanol, centrifuge at 13,000rpm for 15min, Gently pour off the supernatant; centrifuge at 3000rpm for 10sec, shake off the remaining liquid on the tube wall to the bottom, blot dry with a micropipette, and dry at room temperature for 2-3min (do not overdry to prevent insoluble nucleic acid in the next step); add 40ul DEPC water ( Add DEPC pu...
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