There is DNA contamination somewhere in your PCR assay system. Use only PCR-grade reagents and lab ware. Wear gloves throughout the procedure. Always use fresh pipette tips, water and other reagents. Do not leave lab ware (open tubes and tip boxes) exposed to the air for long periods of time. The most common source of DNA contamination comes from the PCR products of previous experiments. Avoid the spread of any PCR products into the air of your working environment. Close all tubes containing PCR products once you are finished adding or removing volumes. Discard all tips or tubes that have been in contact with PCR products into a container of bleach. Clean your bench and your pipettors often. Some researchers expose lab ware with UV light to render any contaminating DNA ineffective in PCR through the formation of thymidine dimers.
Recent Posts
- How to Improve 2A Linker Cleavage Efficiency
- AAVhu.14 Capsid Protein VP1 (Cap) Gene
- AAVhu.32 Capsid Protein VP1 (cap) Gene
- AAVhu68 Capsid Protein (VP1) Gene
- AAVrh.74 Capsid Sequence
- How to avoid cross-contamination in qPCR
- Reduce the risk of cross-contamination from the amplicon/template and previous reactions for a qPCR
- Difference between dye-based vs probe-based qPCR
- OmpA Signal for Protein Expression
- Isopycnic Centrifugation
- High-cell-density cultivation (HCDC)
- Is Kozak sequence essential for transgene expression in lentivirus?
- How to remove protein from PEG precipitated lentivirus
- Primers and probes used for rAAV quantitative analysis
- Quantification for residual host cell DNA contamination in the rAAV prep via qPCR or ddPCR analysis targeting highly repetitive genome sequences
- How to protect RNA from degradation?
- What is the main reason for RNA being unstable?
- Why Are Transgenes Cloned into Lentiviral Vectors Without a Poly(A) Signal?
- AAV(Myo1A)-CMV-GFP Ready to Package
- Potential Reasons for Lack of Supercoiled DNA
- Transfection Efficiency: What Makes Plasmid DNA Transfection Grade
- Why Uncut Plasmid DNA on Agarose Gel Has 3 Bands
- AAV6.2-CMV-GFP and AAV6.2-CMV-iCre Ready to Package
- LV-Syn-GFP-shRNAmir-WPRE Ready to Package to Knock Down Gene Expression in Neurons
- AAV(cc47)-CMV-GFP is Ready to Package
- AAV(MYO)-CMV-GFP is Ready to Package
- AAV(REC2)-CMV-GFP is Ready to Package
- AAV Rh20 VP1 Gene
- AAV Rec2 Capsid Sequence
- Homemade qPCR Mix Recipe
- Home made qPCR Master Mix
- Nanopore Sequencing: Principles, Platforms and Advantages
- Nanopore Sequencing
- ssAAV9-CMV-SecNanoLuc & scAAV9-CMV-SecNanoLuc, Ready to Package
- AAV(BI30)-CAG-GFP-3xmiR122 is Ready to Package for the Transduction of the Endothelial Cells of CNS
- AAV(9-X1.1)-CMV-GFP is Ready to Package for the Transduction of the Endothelial Cells of CNS