Kit for detecting copy number variation of PLP1 gene
A gene copy number, PLP1 technology, applied in the field of biomedical detection, can solve the problems of high sensitivity and unsuitable for high-throughput detection, and achieve the effect of low pre-experimental cost
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[0041] 1, primer test
[0042] 1) Linear DNA Preparation (Table 1): Dilute the standard Human Genetic DNA (253NG / UL) gradient, take 13 ul DDH 2 O, vortex, slightly, concentration is 66 ng / ul.
[0043] Then 10 times gradient dilution, add 20 ul to 180 ul DDH 2 O, each time you need full vortex mixing to make the next gradient dilution.
[0044] Table 1
[0045]
[0046] 2) Experimental system (Table 2)
[0047] Table 2
[0048]
[0049] 3) Amplification procedure (Table 3)
[0050] table 3
[0051]
[0052] 4) Result analysis
[0053] ABI7500 setting:
[0054] Experiment PROP Select QuantuTation-Relative Standard Curve and Sybrgreen Reagents.
[0055] The results are as follows:
[0056] Primer OTC-L: primer amplification efficiency 92.6%, solubilized peak single;
[0057] Primer OTC-M: primer amplification efficiency 99%, solubilized peak single;
[0058] Primer OTC-R: primer amplification efficiency of 93.1%, solubolic peak single;
[0059] Primer RP: primer amplification...
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