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Genome editing ÀÌÈÄ mutation È®Àοë

Mutation Detection Kit

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Clontech
631443
Guide-it¢â Mutation Detection Kit
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100 rxns
772,000¿ø 
965,000¿ø
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11.01 ~ 12.27
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x32691, x33142, x33143
Clontech
631448
Guide-it¢â Mutation Detection Kit
°ü·ÃÇмú ±¸¸ÅÇϱâ
25 Rxns
361,600¿ø 
452,000¿ø
°¡°ÝÇÒÀÎ
11.01 ~ 12.27
Á¦Á¶»ç ÆäÀÌÁö·Î ¹Ù·Î°¡±â



  • CRISPR/Cas9, ZFNs, TALENsÀ» ÀÌ¿ëÇÑ genome editing ÀÌÈÄ º¯ÀÌ µµÀÔ È®Àο¡
  • Genome¿¡ µµÀÔµÈ »ðÀÔ (Insertion), °á½Ç (Deletion)À» PCR¹ýÀ¸·Î ½±°Ô °ËÃâ
  • ¼¼Æ÷·ÎºÎÅÍ Á÷Á¢ PCR ÁõÆøÀÌ °¡´ÉÇÏ¿© ½Å¼ÓÇÏ°í ³ôÀº È¿À²
  • Mutation detection¿¡ ÇÊ¿äÇÑ ¸ðµç Á¦Ç°ÀÌ ±¸¼ºµÈ complete kit
Á¦Ç°¼³¸í
Guide-it Mutation Detection Kit´Â zinc-finger nucleases (ZFNs), transcription-activator-like effector nucleases (TALENs), or CRISPR/Cas9À¸·Î ó¸®µÈ cell genomeÀ¸·ÎºÎÅÍ PCR ¹æ¹ýÀ¸·Î »ðÀÔ ¶Ç´Â °á½Ç º¯ÀÌ (Insertions or deletions: Indel)¸¦ È®ÀÎÇÒ ¼ö ÀÖ´Â Á¦Ç°ÀÌ´Ù. º» Á¦Ç°Àº Terra PCR Direct Polymerase Mix (Code 639269)¸¦ »ç¿ëÇÏ¿© º°µµÀÇ DNA ÃßÃâ °úÁ¤ ¾øÀÌ ¼¼Æ÷·ÎºÎÅÍ target sequence¸¦ ÁõÆøÇÒ ¼ö ÀÖ´Ù. ÁõÆø »ê¹°Àº Guide-it Resolvase¿¡ ÀÇÇØ mismatch ¼­¿­ÀÌ Àý´ÜµÇ¸ç, À̸¦ Àü±â¿µµ¿À¸·Î °ËÃâÇÔÀ¸·Î½á À¯ÀüÀÚ º¯ÀÌÀ» ½±°Ô È®ÀÎÇÒ ¼ö ÀÖ´Ù.



±×¸² 1. The Guide-it Mutation Detection Kit is used to confirm the presence of mutations in genomic DNA. In the first step your target sequence is amplified directly from your target cells using the Terra PCR Direct Polymerase included in the kit, so there is no need to extract and purify genomic DNA from your cell population prior to amplification of your target sequence. The amplicon is then melted and hybridized to form the mismatched targets that can be cleaved by the Guide-it Resolvase.



±×¸² 2. Comparison of the Guide-it and Surveyor assays for detecting mutations in mammalian cells. 293T cells were transfected with plasmids encoding Cas9 and a sgRNA specific for the AAVS1 locus. Transfected cells were harvested 48 hr post-transfection and mixed with untransfected cells at varying ratios. An amplicon containing the targeted AAVS1 locus was generated using Terra Direct Polymerase Mix and the PCR products were purified and cleaved using either Guide-it Resolvase or the Cel1 enzyme (Surveyor assay). Mutations were easily discernable when using the Guide-it kit. In contrast, the Surveyor Assay showed considerable smearing, making it difficult to determine cleavage efficiency and reducing the ability to detect low levels of mutation.
Àû¿ë
  • Confirmation of mutations caused by Cas9/CRISPR, TALENs, or zinc-finger nucleases
  • Detecting insertions and deletions in mammalian genomic DNA
±¸¼ºÇ° (ÀÚ¼¼ÇÑ ³»¿ëÀº CoA¸¦ ÂüÁ¶Çϼ¼¿ä)
  • Extraction Buffer 1
  • Extraction Buffer 2
  • Guide-it Resolvase
  • Terra PCR Direct Polymerase Mix (1.25 U/¥ìl)
  • 2X Terra PCR Direct Buffer (with Mg2+, dNTP)
  • PCR-Grade Water
  • Positive Control DNA for Resolvase
º¸Á¸
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Keyword : Mutation,Indel,Insertion,deletion,KO,Knockout,Knock out, Knock-out,KI,Knock-in,Knock in,knockin,CRISPR,CRISPR/Cas9,Cas9,sgRNA,Å©¸®½ºÆÛ,gene editing,À¯ÀüÀÚÆíÁý

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