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DNA-蛋白質(zhì)互作研究方法

瀏覽次數(shù):842 發(fā)布日期:2022-6-23  來源:本站 僅供參考,謝絕轉(zhuǎn)載,否則責任自負

Cleavage Under Target & Tagmentation (CUT&Tag)是一種新興的DNA-蛋白質(zhì)互作研究方法。CUT&Tag以融合了protein A/G的Tn5轉(zhuǎn)座酶為核心,融合蛋白通過protein A/G與抗體結合,使得Tn5被栓系在靶位點周圍,從而在目的位點附近進行酶切反應,并同時引入二代測序所必需的接頭序列,產(chǎn)物DNA經(jīng)過后續(xù)提取與PCR擴增后,得到直接用于測序的文庫。CUT&Tag與傳統(tǒng)的ChIP-Seq技術相比較,實驗不需要超聲打斷,也不需要傳統(tǒng)的連接法添加測序接頭,操作簡單、周期短、信噪比高、重復性好、細胞用量少,為極低起始細胞量和單細胞測序研究提供了可能性。

產(chǎn)品引用文獻:

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The chromatin accessibility landscape reveals distinct transcriptional regulation in the induction of human primordial germ cell-like cells from pluripotent stem cells[J]. Xiaoman Wang et al. Stem Cell Reports. 2021.

Cellular senescence in hepatocellular carcinoma induced by a long non-coding RNA-encoded peptide PINT87aa by blocking FOXM1-mediated PHB2[J]. Xiaohong Xiang et al. Theranostics. 2021.

Gastrin, via Activation of PPARα, Protects the Kidney Against Hypertensive Injury[J]. Daqian Gu et al. Clinical Science. 2021.

Alpha‐fetoprotein accelerates the progression of hepatocellular carcinoma by promoting Bcl‐2 gene expression through an RA‐RAR signalling pathway[J]. Chao Zhang et al. Journal of Cellular and Molecular Medicine. 2020.

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