Kit used for detecting candida krusei in intestinal tract by fluorescence quantitative PCR method
A Candida krusei, fluorescence quantitative technology, applied in the direction of fluorescence/phosphorescence, microorganism-based method, microorganism determination/inspection, etc., can solve the problems of long diagnosis cycle, low detection sensitivity, etc. Good specificity
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specific Embodiment 1
[0033] The test kit in this embodiment includes:
[0034] 10×Taqman PCR buffer of 1 / 10 of the total reaction volume;
[0035] Each 0.15 μmol / L upstream and downstream primers;
[0036] Each 200μmol / L dATP, dTTP, dGTP, dCTP;
[0037] 2.0mmol / L MgCl 2 ;
[0038] 0.05U / μl HOTSTART Taq DNA polymerase;
[0039] 0.02×SYBR green I fluorescent dye;
[0040] Standard positive template, its concentration is serially diluted according to the requirements of quantitative standard curve preparation;
[0041] The balance is sterile double distilled water.
specific Embodiment 2
[0042] The kit components are as follows:
[0043] 10×Taqman PCR buffer of 1 / 10 of the total reaction volume;
[0044] Each 1.0 μmol / L upstream and downstream primers;
[0045] Each 200μmol / L dATP, dTTP, dGTP, dCTP;
[0046] 3.5mmol / L MgCl 2 ;
[0047] 0.05U / μl HOTSTART Taq DNA polymerase;
[0048] 0.02×SYBR green I fluorescent dye;
[0049] Standard positive template, its concentration is serially diluted according to the requirements of quantitative standard curve preparation;
[0050] The balance is sterile double distilled water.
specific Embodiment 3
[0051] The kit components are as follows:
[0052] 10×Taqman PCR buffer of 1 / 10 of the total reaction volume;
[0053] Each 0.5 μmol / L upstream and downstream primers;
[0054]Each 200μmol / L dATP, dTTP, dGTP, dCTP;
[0055] 3.0mmol / L MgCl 2 ;
[0056] 0.05U / μl HOTSTART Taq DNA polymerase;
[0057] 0.02×SYBR green I fluorescent dye;
[0058] Standard positive template, its concentration is serially diluted according to the requirements of quantitative standard curve preparation;
[0059] The balance is sterile double distilled water.
[0060] The working principle of the kit of the present invention is introduced:
[0061] In the PCR reaction system, adding excess SYBR fluorescent dye, SYBR fluorescent dye specifically incorporated into DNA double strands, emits a fluorescent signal, and the SYBR dye molecules that are not incorporated into the strand will not emit any fluorescent signal, thus ensuring the fluorescent signal The increase of is fully synchronized with th...
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