Ultra-Sensitive mutation screening test for Colorectal Cancer via a Simple Blood Draw
The UltraCHECK Colon Panel v2.0 enables mutation detection in liquid biopsy samples as low as 0.1% allele frequency. This targeted highly sensitive panel identify mutations across heterogeneous tumor samples, circulating cell-free DNA (ctDNA) or circulating tumor cells (CTCs), responsible for colorectal cancer.
|BRAF||Codon 469 of exon 11; codons 594, 600 of exon 15||5|
|EGFR||Extracellular domain mutations across exon 12||10|
|KRAS||Codons 12, 13 of exon 2; codons 59, 61 of exon 3; codons 117, 146 of exon 4||48|
|NRAS||Codons 12, 13 of exon 2; codons 59, 61 of exon 3; codons 117, 146 of exon 4||40|
|PIK3CA||Codons 542, 545 of exon 9; codon 1047 of exon 20||4|
Covers 100 + mutations across 5 key oncogenes.
Can detect mutations as low as 0.1% allele frequency.
Can utilise as low as 10ng input DNA.
Covers clinically relevant genomic alterations which enables physicians to personalize therapy for a patient.
FREE Sample Collection
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