MGB Eclipse¢ç Probes and Primers

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.

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Specifications

  • Fluorophores: FAM, HEX¢â, TET¢â, or Yakima Yellow¢â dyes

  • Full sequences Á¦°ø

  • Normalized final yield: 6nmole, 20nmole,  50nmole

  • Length: typically 13-20 bases

  • Turnaround time: 4-5 weeks

 Dye - Quencher

 Final yield

 6nmole

 20nmole

 50nmole

 FAM - MGB Eclipse

 

 HEX - MGB Eclipse


 TET- MGB Eclipse

 

 YAK - MGB Eclipse

 Inquire

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 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.

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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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