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Product Infomation | |
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Features: | Quality Standards (1)Allele Frequency (AF) Genotype is tesed by Droplet Digital PCR, the acceptance criteria as follows: AF=0%, acceptable range ≤ 0.1%; AF < 5%, acceptable margin of error = ± 30%; 5% ≤ AF < 10%, acceptable margin of error = ± 20%; 10%≤AF, acceptable error range = ±10%. (2)Integrity is tesed by Agarose gel electrophoresis, the acceptance criteria as follows: Bright band of high molecular weight. SNV: AKT1 E17K,BRAF V600E,EGFR G719S,EGFR L858R,EGFR T790M, KIT D816V,KRAS A146T, KRAS G12D,KRAS G13D,NRAS Q61K, PIK3CA E545K,PIK3CA H1047R,KRAS G12C,KRAS G12V,EGFR L861Q,EGFR S768I, KRAS G12S, KRAS G12R,KRAS G12A,EGFR G719A,NRAS Q61R,FGFR3 Y375C. Deletion: EGFR ΔE746_A750,FLT3 ΔI836,MET Exon 14 Skipping. Insertion: EGFR A767_V769dup. Fusion: CD74(6)-ROS1(34),EML4(6)-ALK(20), EML4(13)-ALK(20). CNV: MET Amplification, ERBB2 Amplification. |
Method: | Quality Control Method: ddPCR |
Concentration: | 30 ng/µL |
Application: | CD Tumor SNV Wild Type gDNA Standard is mainly used as a negative control for gDNA variant detection during second-generation sequencing. It can be used in combination with Tumor Structure Variant 5% gDNA Standard and Tumor SNV 5% gDNA Standard. |
Preservation Solvent: | Tris-EDTA (10mM Tris-HCl, 1mM EDTA), pH 8.0 |
Storage: | Store at 2-8℃, 36 months. |
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