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脆性X綜合征相關(guān)蛋白AFF1重組兔單抗

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

  • 產(chǎn)品型號：bsm-61466R
  • 廠商性質(zhì)：生產(chǎn)廠家
  • 更新時間：2025-03-01
  • 訪  問  量： 54

詳細介紹

Human,Mouse,Rat
WB,IHC-P,IHC-F,ICC/IF,IF,Flow-Cyt
Store at 4℃ for short term. Store at -20℃ for long term. Avoid repeated freeze/thaw cycles.

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