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  • 產(chǎn)品名稱:FMR1抗原(重組蛋白)

  • 產(chǎn)品型號(hào):1mg
  • 產(chǎn)品廠商:通蔚生物
  • 產(chǎn)品價(jià)格:3580
  • 產(chǎn)品庫存:35
  • 產(chǎn)品文檔:
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FMR1抗原(重組蛋白)公司秉承“專注品質(zhì)、信守承諾、積極溝通、chuang新服務(wù)”的企業(yè)文化積極參與生物領(lǐng)域的技術(shù)chuang新和技術(shù)服務(wù),力求為我國科研事業(yè)添磚加瓦,嚴(yán)格的質(zhì)控體系,建立和完善企業(yè)制度,創(chuàng)造性發(fā)展,客戶的滿意就是我們的宗旨。
詳情介紹:
中文名稱: FMR1抗原(重組蛋白)

英文名稱: FMR1 Antigen (Recombinant Protein)

別     名:  POF; FMRP; POF1; FRAXA

儲(chǔ)     存:  冷凍(-20℃)

相關(guān)類別: 抗原

概     述:

Fusion protein corresponding to a region derived from 1-294 amino acids of human FMR1

技術(shù)規(guī)格

Full name:

fragile X mental retardation 1

Synonyms:

POF; FMRP; POF1; FRAXA

Swissprot:

Q06787

Gene Accession:

NP_002015

Purity:

>85%, as determined by Coomassie blue stained SDS-PAGE

Expression system:

Escherichia coli

Tags:

His tag C-Terminus, GST tag N-Terminus

Background:

The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene.






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