A primer set, probe set and kit for synchronous detection of pathogens associated with multiple reproductive tract infections
A technology for reproductive tract infection and primer probes, which is applied to the field of primer compositions for pathogens and their kits, can solve the problems of low sensitivity, low sensitivity, and large impact on results, and achieves strong primer specificity and high reverse transcription efficiency. , check the overall effect
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Embodiment 1
[0045] Example 1: Preparation of a multiplex fluorescent quantitative PCR kit for the detection of 15 reproductive tract pathogens
[0046] The multiplex fluorescent quantitative PCR amplification kit used in the detection of 15 kinds of reproductive tract pathogens of the present invention, the composition of the PCR amplification kit is shown in Table 1.
[0047] Table 1 Composition list of PCR amplification kit
[0048]
[0049] The kit of the present invention can be used to detect 15 kinds of reproductive tract pathogens: herpes simplex virus type 1 (HSV1), herpes simplex virus type 2 (HSV2), group B streptococci (SAg), atopobium (AV), common Revobacterium (PV), Megasphaerum (ME), Motonia (MB), Neisseria gonorrhoeae (NG), Gardnerella (GV), Trichomonas vaginalis (TV), Treponema pallidum (TP) , Candida albicans (CA), Ureaplasma urealyticum (UU), Chlamydia trachomatis (CT), Mycoplasma hominis (MH) nucleic acid.
[0050] The design of 15 kinds of reproductive tract patho...
Embodiment 2
[0075] Embodiment 2: the detection method of multiplex fluorescent quantitative PCR kit
[0076] 1. Detection kit
[0077] The multiplex fluorescent quantitative PCR kit prepared in Example 1 for the detection of 15 kinds of reproductive tract pathogens.
[0078] Detection object
[0079] 2.1 Preparation of internal standard granule normal saline containing housekeeping gene (hereinafter referred to as "internal standard normal saline"): Measure 800mL of normal saline (0.9% sodium chloride solution) into a 1000mL volumetric flask in the reference substance preparation room in the clean work area , adding 5.0×10 9 Copies / mL pathogen plasmid or particle 1mL, dilute to 1000mL with normal saline, turn over to mix well, so that the final concentration is 5.0×10 6 copies / mL. Transfer the above solution to a 1000mL beaker and divide it for use.
[0080] 2.2 7 samples to be tested were negative
[0081]Collect cervicovaginal secretion samples such as HPV16, HPV18, HPV51, ciliat...
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