Competitive Allele-Specific Probe Genotyping Master Mix with UDG
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Competitive Allele-Specific Probe Genotyping Master Mix with UDG

Cat.No: NATR-HMM-0200 Datasheet

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Product Name Competitive Allele-Specific Probe Genotyping Master Mix with UDG
Catalog No. NATR-HMM-0200
Description A one-bottle probe-based genotyping master mix that combines competitive allele-specific amplification, dual-color fluorescence and thermolabile UDG carryover control.
Intended Use SNP and InDel genotyping; plant breeding; pharmacogenomics; high-throughput sample screening.
Principle / Technology Two allele-specific forward primers, one common reverse primer and two fluorescent probes generate allele-dependent FAM/HEX endpoint signals. A dUTP/thermolabile UDG system removes uracil-containing carryover products at room temperature and rapidly inactivates at 50–55°C.
Detection Method Dual-color endpoint fluorescence allelic discrimination using FAM and HEX channels.
Sample Type Purified or crude-extracted genomic DNA from multiple species.
Performance Range / Specifications Available in 1, 5 and 25 mL formats. Reported evaluations of SNP and InDel targets showed 100% sample detection and 100% genotyping accuracy in the tested datasets; carryover-template removal exceeded 99.99% in the reported test.
Sensitivity / LOD High target detection rate across tested SNP and InDel assays.
Specificity Strong allele discrimination and well-separated genotype clusters for SNP and InDel loci.
Reaction Conditions / Protocol Prepare allele-specific and common primers with the required reporter-tail design, combine with DNA and master mix, run PCR, and analyze terminal FAM/HEX fluorescence clusters.
Components / Formulation One-bottle competitive allele-specific probe genotyping master mix with dUTP/thermolabile UDG; available in low-ROX, no-ROX and high-ROX formulations.
Storage Conditions Store at −30 to −15°C protected from light.
Package Specifications 1 mL; 5 mL; 25 mL.
Product Form Ready-to-use probe genotyping master mix.
Quality Control Detection rate, genotype accuracy, cluster separation, crude-template compatibility and carryover-removal performance are evaluated by genotyping PCR.
Key Features Accurate SNP/InDel genotyping; broad crude-DNA compatibility; three passive-reference options; room-temperature carryover removal; high-throughput format.
Shipping Conditions Ship at or below 0°C.
Compatibility Low-, no- and high-passive-reference formulations support different real-time PCR instrument classes and multi-species DNA samples.
Application Notes / Precautions Recommended amplicon length is 45–120 bp and should not exceed 150 bp. Target-product Tm is typically 63–75°C; primer GC content is preferably 40–60%. Allele-specific forward primers require distinct 5′ reporter-tail sequences.
Genotype SNP and InDel biallelic genotyping.

For research use only, not for clinical use.

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