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FMR2/AFF2/FRAXE from Gene Link


FMR2/AFF2/FRAXE FRAXE mental retardation is the cause of a non-syndromic X-linked mental retardation affecting 1/50,000 newborn males. The CCG repeat of FRAXE can either expand or contract and is equally unstable when transmitted through the male or the female germ line.
The detection of amplification/expansion of a region of DNA sequence can be detected by PCR and Southern, these methods can be used for all disorders involving increase in size of a region of DNA. Southern blot analysis for FRAXE mutation detection involves the cleavage of DNA with enzyme Not I and Afl III. This method detects the size of CCG repeats region by hybridization of AFF2 AJ31-Dig1 GeneProber to DNA that has been double digested with restriction enzymes Not I and Afl III and blotted onto a membrane. In normal females two fragments are seen, a 2.2kb corresponding to the active X and a 4.8kb fragment corresponding to the methylated inactive X chromosome. Normal males exhibit only the 2.2kb banding pattern. Affected males will have an amplified CCG repeats region with methylation thus giving rise to fragments larger than the normal 4.8kb. Premutations in males and females will be seen as fragments from 2.3-3.3kb (normal 2.2kb) derived from the X chromosome. Premutations in females derived from the inactive X will give fragments from 4.9- ~6kb. Mosaicism is characterized by fragments appearing as a mixture of full mutation (methylated, larger than 4.8kb) and unmethylated premutation (2.2-3.3kb). Gene Link has developed non-radioactive detection methods probe for Southern blot and GScan PCR based methods for fluorescent detection and Genemer kits for agarose gel based detection kits.

   Catalog No.    ProductPDF GuideManualMSDSSizePrice.Quantity 
40-2054-41FRAXE/FMR2/AFF2 CCG Repeat Genotyping GeneProberTM AFF2-AJ31Dig1 110 uL$673.00
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