VE-D050T Vero Host Cell DNA Residue Detection kit
The Vero Host Cell DNA Residue Detection Kit can be used for Quantitative analysis of DNA residue in recombinant protein expressed products, purified intermediate and finished products from the host cell.
Introduction |
This kit adopts Taqman probe fluorescence qPCR method. The kit has the advantages of high specificity and sensitivity by using specific primers & probes, LOQ can reach 1fg/μL level. The preparation process of DNA Control is completely consistent with that of other host cell DNA national standards, therefore it has high purity and no protein and ion interference to ensure the accuracy of the sample quantitative detection. The kit provides DNA Dilution Buffer, which enables good replicate parallelism in a single experiment and good reproducibility between multiple experiments. |
| Kit Components | ||
DNA Amplification | ||
Components NO. | Components Name | Cat#/Size VE-D050T(50T) |
B1 | 2XqPCR Mix | 0.625mL |
B2 | Primer&Probe Mix | 100μL |
B3 | 2×1.5mL | |
B4 | DNA Control (10ng/μL) | 25μL |
B5 | RNase-Free H2O | 0.5mL |
B6 | 50X ROX Reference Dye(Optional) | 0.15ml |
Shipping and Storage | |
| 1 | All components are shipped on dry ice. |
| 2 | The kit should be stored at -20℃ and it is recommended to be used within one year. B2 should be stored protected from light. |
| 3 | B2/B3/B4 can be stored at -20℃ for 2 years, while B1/B5/B6 can be stored at -20℃ for 1 year. B1/B5/B6 can also be purchased together as a separate set. |
Accuracy (Standard: ≦30%) | Intra Variation% 4.8-12.5 |
Inter Variation% 14-17 | |
Recovery% | 102-117 |
| Limit of Quantitation | 1 fg/μL |
Specificity | - |
Components | Volume(μL) |
2XqPCR Mix | 12.5 |
Primer&Probe Mix | 2 |
DNA template (control or sample) | 5 |
Add water | 5.5 |
Total Volume | 25 |
Mix solution = (number of reaction wells+4) * (12.5+2+5.5)μL (including the volume lost in the 4 wells).
The detection range of the standard curve mentioned above is suitable for most experiments and can be adjusted as needed, such as 30fg/μL-300pg/μL.
Standard Curve: R ²> 0.99; Amplification Efficiency: 90% ≤ Eff% ≤ 110%; Slope: -3.8~-3.1.
The recovery rate of spiked samples=(measured value of spiked samples - measured value of samples)/theoretical value of spiked samples * 100%, with a range of 50% -150%.
No Template Control (NTC): In the reaction system, replacing the target template with DNA Dilution Buffer while keeping other components unchanged, and the Ct value obtained should be 'Undetermined' or Ct value≥35.
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