脆性X綜合征相關(guān)蛋白AFF1重組兔單抗

Name: 脆性X綜合征相關(guān)蛋白AFF1重組兔單抗bsm-61466R
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簡要描述：Fragile X syndrome is the most frequent form of inherited mental retardation and is the result of transcriptional silencing of the FMR1 gene on the X chromosome. The FMR1 gene contains a distinct CpG dinucleotide repeat located in the 5' untranslated region of the gene. In fragile X syndrome this tandem repeat is substantially amplified and subjected to extensive methylation and enhanced transcriptional silencing. The FMR1 protein (or FMRP) is an RNA-binding protein that associates with pol