Residual DNA Detection
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PerfectStart® CHO DNA Quantification Kit

Product Details

This product is used for quantitative detection of CHO cell DNA remaining in various biological products.
The principle of this product is that the amount of nucleic acid in the sample is determined by the detection of the intensity of fluorescence which is proportional to the amount of amplified product during the amplification process by adding a fluorescent probe (TaqMan or Molecular Beacon, etc.) to the PCR system. CHO qPCR SuperMix (2×) in this product contains PerfectStart Taq hot start enzyme (uses 3 monoclonal antibodies to efficiently bind with Taq DNA Polymerase, effectively blocking DNA polymerase activity and preventing non-specific amplification at low temperature), qPCR reaction buffer, dNTPs, PCR enhancer and stabilizer specially optimized for CHO cell DNA detection. In addition, a dUTP/UDG system is introduced into this reaction mix, which can degrade U-containing ssDNA and dsDNA before reverse transcription, eliminating cross-contami- nation caused by PCR products.

· High specificity, high sensitivity, high amplification efficiency enabled by 3 kinds of blocking antibodies, and suitable for a 
wide range of samples.

· Specially optimized qPCR reaction buffer to provide higher extension speed, sensitivity and specificity.
· The use of UDG enzyme and dUTP can effectively prevent cross-contamination of PCR products to ensure accurate data.

at -20 ℃ for two years

Dry ice (-70 ℃)

Product Contents

CHO qPCR SuperMix (2×)
2 × 750 μl
PCR enzymes, dNTPs, magnesium ions, PCR buffer, etc.
6 × CHO Primer Probe Mix500 μlCHO DNA primer probe
CHO Standard S0100 μlCHO standard DNA
Standard Diluent

3 × 1 ml

Nuclease-free Water1 ml

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