IDT¿¡¼ Á¦°øÇÏ´Â MGB Eclipse¢ç Probes´Â ISO 13485 ÀÎÁõÀÌ Æ÷ÇÔµÈ GMP ½Ã¼³¿¡¼ ÇÕ¼ºÇÑ human IVD Àü¿ëÀ¸·Î¸¸ »ç¿ëÇÒ ¼ö ÀÖ´Â probeÀÔ´Ï´Ù. PCRÀº ºÐÀÚ Áø´Ü ±â¼ú¿¡ ÀÖ¾î ¸Å¿ì Áß¿äÇÑ ½ÇÇè Áß ÇϳªÀ̸ç, gold standard qPCR(5¡¯ nuclease assays)ÀºMGB(minor groove binder)±â¼úÀ» µµÀÔÇÑ probe¸¦ »ç¿ëÇÑ ±â¹ýÀÔ´Ï´Ù. ´Ù¾çÇÑ Çü±¤À» »ç¿ëÇÏ¿© multiplex·Î µðÀÚÀÎÀ» Çϱ⠽±°í MGB´Â hybridizationÀ» ¾ÈÁ¤ÈÇÏ°í Tm°ªÀ» ¿Ã·Á°¡ ªÀº ¿Ã¸®°í°¡ AT-rich regionÀ» detectionÇϰųª allelic discriminationÀ» Çϴµ¥ ¸Å¿ì ÀûÇÕÇÕ´Ï´Ù.
Specifications
Dye - Quencher Final yield 6nmole 20nmole 50nmole FAM - MGB Eclipse HEX - MGB Eclipse TET- MGB Eclipse YAK - MGB Eclipse Inquire Inquire Inquire Comparison qPCR studies of multiple MGB¢â probe and primer sets manufactured by IDT versus those made by another leading manufacturer demonstrated equivalent genotyping calls for KRAS mutations and high specificity for the appropriate wild-type or mutant allele (Figure 1). End-point fluorescent signal intensities were similar or slightly higher using MGB Eclipse¢ç Probes from IDT. Figure 1. Genotyping Results From KRAS G12R qPCR Assays Using Probe and Primers Manufactured by IDT and Another Leading Manufacturer. The KRAS G12R qPCR assays used MGB Eclipse¢ç probes (FAM dye—wild-type probe; TET¢â dye—mutant probe) and primers made by either IDT or another leading manufacturer (Company L). Reactions (10 µL) were run with 104 copies of wild-type, mutant, or pooled wild-type/mutant template (IDT¢ç gBlocks¢ç Gene Fragments) and TaqMan¢ç Gene Expression Master Mix (Life Technologies) on a CFX384 Touch¢â Real-Time PCR Detection System (BioRad). Cycling conditions were 3 min. 95¡ÆC; 50 x (10 sec. 95¡ÆC, 30 sec. 60¡ÆC). |
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