FRagile x pcr
I am currently trying to standardise FMR1 gene mutation by PCR method. the region is highly repititive for CGG repeats and highly gc rich. I am using long primers 35nt length with high GC content > 85%, and tm 80 and 92. I am using the roche expand long template pcr kit with buffer 2 and high fidelity polymerase with hotstart method . I tried the conditions as 98X10min, 98X45 sec,64X1 min,68x2min and 68x 7 sec. Itried betaine in the concentration of 1.7-2.2 molar and q soltion , DMSO 10 %, but did not get any ampification . Then i tried various mgcl2 with 2.5-4 millimol. still no band.
I carrried the reaction with qiagen hot start , still no amplification. IF anyone worked with it lease help me:icon_question:
Re: FRagile x pcr
A group of mutations characterized by trinucleotide repeat expansion causes human diseases such as the Fragile X syndrome, Huntington disease (HD), and myotonic dystrophy. Methods based on PCR amplification of the CGG and CAG repeats region could facilitate the development of a rapid screening assay; unfortunately, amplification across CGG and CAG repeats can be inefficient and unreliable due to the G + C base composition. [Only registered and activated users can see links. Click Here To Register...]
|All times are GMT. The time now is 08:39 PM.|
Powered by vBulletin® Version 3.8.4
Copyright ©2000 - 2015, Jelsoft Enterprises Ltd.
Copyright 2005 - 2012 Molecular Station | All Rights Reserved