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Principle for High Specificity & Accuracy
Compared with 2 × Scarlet™ Blood Direct PCR Mix (EDTA), dTTP is replaced by dUTP in the HS version, and UNG enzymes (Uracil-N-glycosylase) capable of degrading dUTP-containing templates are added at the same time. Before the PCR reaction, UNG enzymes are used to degrade the uracil-containing PCR products. UNG enzymes do not cause any impact on the uracil-free template, thus ensuring the specificity and accuracy of amplification as well as preventing the possible contamination of PCR products during large-scale gene detection.
Features
lThe whole blood is directly used as a PCR template, without time-consuming and expensive DNA purification and pretreatment.
lThe system has strong amplification ability and can sensitively detect genomic and exogenous DNA fragments in the blood.
lThe 2 × Scarlet™ HS Blood Direct PCR Mix (EDTA) provided by this kit has strong inhibitor tolerance.
lThe sample is operated in a fully enclosed condition, preventing either sample contamination or false positive PCR results.
l2 × Scarlet™ HS Blood Direct PCR Mix (EDTA) can effectively eliminate the contamination caused by PCR products and ensure the specificity and accuracy of amplification.
lThe Scarlet™ HS Blood Direct PCR Kit (EDTA) is specially designed for direct PCR identification of EDTA anticoagulant whole blood.
lAmplified fragments should be less than 1 kb. If more than 1 kb, the amplification efficiency may decrease or the amplification may even fail.
lThe PCR products obtained from this kit should not be used for gene cloning or sequencing.
lPCR products may have mutation.
lThe 3' end of the PCR product is randomly added with A tail.
If used frequently, 2 × Scarlet™ HS Blood Direct PCR Mix (EDTA) can be stored at 4°C for a short time (within 10 days). For long term storage, please keep it at - 20°C.
6 × DNA Loading Buffer can be stored at 4°C or - 20°C for a long time.
Instruction: Protocol
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