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儀表網(wǎng)>產(chǎn)品庫>生命科學儀器>分子生物學儀器>其它分子生物學儀器>siPOOLs用于藥物靶點篩選研究(RNAi)
  • siPOOLs用于藥物靶點篩選研究(RNAi)
  • siPOOLs用于藥物靶點篩選研究(RNAi)
  • siPOOLs用于藥物靶點篩選研究(RNAi)
  • siPOOLs用于藥物靶點篩選研究(RNAi)
  • siPOOLs用于藥物靶點篩選研究(RNAi)

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siPOOLs用于藥物靶點篩選研究(RNAi),經(jīng)證明可有效消除脫靶效應,并提高結果的可靠性(Hannus et al., 2014)。Pack Hunter (pooling) 方法通過將當個siRNA的濃度稀釋到刺激表型的閾值以下來對抗單個siRNA的脫靶。
siPOOLs用于藥物靶點篩選研究(RNAi) 產(chǎn)品詳情

 

 

siPOOLs用于藥物靶點篩選研究(RNAi)

 

對于靶向基因沉默,RNA干擾(RNAi)具有易于操作、快速結果、高效率、廣泛適用于各種細胞類型的多重優(yōu) 勢。其具有瞬轉效應和劑量依賴效應,這點與小分子非常相似。然而,目前的siRNA試劑其特異性和基因沉默 效率可變,阻礙了它們作為藥物發(fā)現(xiàn)和基因研究工具的應用。

siTOOLs Biotech由Michael Hannus博士和Gunter Meister教授于2013年9月成立,由德國雷根斯堡大學 和Intana Bioscience制藥服務公司聯(lián)合運營。目前推出有3個產(chǎn)品系列:(1)siPOOLs:一種siRNA混合物,有 效增加基因沉默特異性,“稀釋”傳統(tǒng)RNA干擾試劑的脫靶效應。(2)raPOOLs:一種穩(wěn)健的RNA親和純化方 案,適用于基因功能和相互作用的生物化學研究。(3)riboPOOLs:適合任意物種的核糖體RNA去除試劑,高效且經(jīng)濟。


可靠表型的特異性基因沉默工具

siPOOLs是一款經(jīng)過優(yōu)化設計的高復雜性的包含30條siRNA的混合物,經(jīng)證明可有效消除脫靶效應,并提高結果的可靠性(Hannus et al., 2014)。 Pack Hunter (pooling) 方法通過將當個siRNA的 濃度稀釋到刺激表型的閾值以下來對抗單個siRNA的脫靶。 借助專有的設計算法,siPOOLs中的siRNA序列經(jīng) 過優(yōu)化,以實現(xiàn)最大的轉錄本覆蓋率,高效雜交并 對旁系同源基因進行過濾,從而實現(xiàn)高效和特異性 的基因沉默。


siPOOLs產(chǎn)品優(yōu)勢

使用簡單快捷:siPOOLs與多種轉染試劑兼容,幾天內(nèi)就能看 到結果。

高度特異性且有效:siPOOLs在標準細胞系中將脫靶率降低5-25 倍,且在1-3 nM下實現(xiàn)基因敲低率≥70%。

一致的表型:與siRNA相反,由序列非依賴性的siPOOL產(chǎn)生 的表型高度一致。

確保經(jīng)過檢驗:通過RT-qPCR進行siPOOL驗證,如果在 轉染下敲低率低于70%,則有可能重新設計。

使用注釋進行定制設計:專業(yè)的設計,確保優(yōu)化熱力學特性且避免旁系 同源基因。

HPLC純化且無毒:所有siPOOL均經(jīng)過HPLC純化,可降低污染物 和副作用的風險。


關鍵問題:siRNAs的脫靶效應

科學家們一直在使用RNA干擾(RNAi)作為研究基因功能的快速有效的工具。然而,短干擾RNA(siRNA)的脫靶效應和可變性能仍然是一個令人頭疼的缺點,在驗證工作中消耗了寶貴的時間和資源。

638157808712364521244.png

siRNA通常與靶RNA轉錄本互補結合,通過RNAi機制指導其降解。脫靶效應主要是由siRNA模擬內(nèi)源性 基因調(diào)節(jié)因子microRNA(miRNA)引起的。由于miRNA只需要6個堿基種子匹配到3'非翻譯區(qū)(UTR)即可觸 發(fā)轉錄本下調(diào),因此siRNA在通過這種機制處理時可以改變許多意外靶標的表達。


siPOOLs如何提高特異性

單個siRNA或含有3-4個siRNA的低復雜度siRNA庫,經(jīng)常擊中多個脫靶基因并表現(xiàn)出易變的靶基因敲低。 siPOOL是高度復雜且確定的30個siRNA池,每個siRNA以皮摩爾工作濃度存在。因此, · 稀釋了每個siRNA的脫靶特征,提高了靶向特異性。 · 確保了靶基因的協(xié)同敲低,產(chǎn)生更穩(wěn)健、更可靠的結果。

 

638157808723771273149.png

 

使用siPOOL具有更高的特異性

 

使用siPOOL具有更高的特異性.png

特異性好的試劑應僅影響其靶標基因。

HeLa細胞中微陣列的表達譜分析顯示,單個siRNA可以誘導許多脫靶基因(紅點),而針對同一靶基因(綠 點)并包含非特異性siRNA的siPOOL大大降低了脫靶效應。


通過siPOOL實現(xiàn)更好的重現(xiàn)性和有效的敲低效率

 

通過siPOOL實現(xiàn)更好的重現(xiàn)性和有效的敲低效率.png

普通siRNA的敲低效率差異很大。

與單個siRNA相比,針對同一基因的siPOOLs具有相似的敲低效率,表明具有更高的穩(wěn)健性和可重復性(左 圖和中圖:靶RNA水平的實時定量PCR測量的相關圖)。 siPOOLs也表現(xiàn)出有效的基因敲低。在常用的細胞系中,許多基因通常在1 nM濃度下實現(xiàn)75-98%的基 因敲低效率(右圖)。


您可以信賴的表型

 

您可以信賴的表型.png

 

如果RNAi效果可靠且特異,靶向同一基因的兩種試劑應產(chǎn)生相似的表型。

每個基因分別使用兩個siPOOL池,一個來自我們的人類激酶siPOOL文庫,一個是市售的每個基因含3條 siRNAs的文庫,科學家在A549細胞中篩選了36個基因并檢測了細胞活力。僅siPOOLs產(chǎn)生了較好的一致性表型。


siTOOLs生物技術始終致力于幫助學術研究人員、科學家、制藥/生物技術公司和RNAi篩選人員。目前,已幫助許多論文 發(fā)表在《自然》、《細胞》、《自然醫(yī)學》、《科學報告》等頂級期刊上。期待與您的合作,我們將為您的RNA研究提供量身定制 的分子工具。


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關于siPOOLs用于藥物靶點篩選研究(RNAi)的更多信息,歡迎聯(lián)系我們!

關鍵詞:標準 APP NMR
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