Using Taqman probe technology, specific primers and probes were designed based on the M gene of Newcastle Disease Virus (NDV) as the target sequence for the auxiliary detection of NDV nucleic acid in samples. This product introduces a dUTP/UDG mix that degrades U-containing ssDNA and dsDNA, eliminating cross-contamination caused by PCR products. At the same time, a positive internal control (an internal standard, using a VIC reporter group) is set to monitor whether the qPCR reaction contains PCR inhibitors by detecting whether the internal standard is normal to avoid false-negative results.
Storage
at -20°C for two years
Shipping
Dry ice (-20°C)
Bio-Medicine
In Vitro Diagnostics
PCR, RT-PCR, qPCR, qRT-PCR
Restriction/Modifying Enzymes
DNA Molecular Weight Standards
Cloning and Mutagenesis System
Nucleic Acid Purification
Next Generation Sequencing
Gene Expression
Protein Analysis
Protein MW Standards
Cell Culture and Detection
Exosome Related
Serum-free medium
Antibodies
ELISA
Instruments
Residual DNA Detection
