Villin 絨毛蛋白（鼠單克隆抗體）

廣州健侖生物科技有限公司

Villin是與刷狀緣微絨毛的微絲束有關的一種胃腸道相關性細胞骨架蛋白。正常組織中，Villin通常只表達于有刷狀緣的細胞上，如胃腸道上皮細胞、胰腺和膽管上皮細胞以及腎實質的上皮細胞中（特別是近曲小管）。Villin作為腸道特異性參考依據，與CDX2聯合應用，可用于腸上皮來源腫瘤與非腸上皮腫瘤的研究。Villin 也可作為胃腸道神經內分泌腫瘤研究的參考指標。

我司還提供其它進口或國產試劑盒：登革熱、瘧疾、流感、A鏈球菌、合胞病毒、腮病毒、乙腦、寨卡、黃熱病、基孔肯雅熱、克錐蟲病、違禁品濫用、肺炎球菌、軍團菌、化妝品檢測、食品安全檢測等試劑盒以及日本生研細菌分型診斷血清、德國SiFin診斷血清、丹麥SSI診斷血清等產品。

歡迎咨詢

歡迎咨詢

Villin 絨毛蛋白（鼠單克隆抗體）

【產品介紹】

細胞定位：細胞漿/細胞膜

克隆號：CWWB1

同型：IgG

適用組織：石蠟/冰凍

陽性對照：結腸

抗原修復：熱修復（EDTA）

抗體孵育時間：30-60min

Villin

想了解更多的產品及服務請掃描下方二維碼：

【公司名稱】 廣州健侖生物科技有限公司
【市場部】     歐

【】 
【騰訊  】 
【公司地址】 廣州清華科技園創新基地番禺石樓鎮創啟路63號二期2幢101-103室

我們可以這樣描述一個細胞的命運：多能狀態的細胞位于山頂，細胞中的基礎信號網絡就像重力一樣想把細胞拉下山，達到已分化狀態。因此細胞重編程中的挑戰是雙重的：不僅要把已分化的細胞抬上山頂，還要沉默那些吸引細胞分化的因子。
細胞重編程zui初是通過逆轉錄病毒將OSKM引入細胞，不過后來其他組合的轉錄因子也獲得了成功，這說明細胞重編程涉及了復雜的動態過程和狀態轉變。這種方法生成的iPSC存在較高的異質性，會引發細胞突變，重編程效率也比較低。要將iPSC用于臨床，需要考慮避開逆轉錄病毒的其他方法。 (延伸閱讀：Nature發表山中伸彌新成果，iPS校正環狀染色體)
正因如此，人們開發了多種第二代iPS方法，其中已經有一些表現出了更好的安全性。逆轉錄病毒的可重復性和簡便性，使其依然活躍在體外研究中。然而在再生醫學領域，附加體型載體(episomal plasmid)更受青睞。其他方法還包括腺病毒、仙臺病毒、合成蛋白和RNA。不過，這些方法盡管更為安全，但技術要求比較高，對重編程效率也并無改善。zui近有研究顯示，僅通過小分子就可完成細胞重編程。這意味著，間接靶標與多能性有關的分子通路，就足以重新決定細胞的命運。
理解上述分子通路，可以幫助人們防止已進入多能狀態的細胞回到已分化狀態。多能細胞和已分化細胞之間，存在DNA甲基化和組蛋白乙酰化的差異。另外，靶標表觀遺傳學機制的小分子，能夠提升重編程效率。總的來說，在提升重編程效率的工作中需要特別注意表觀遺傳學因子的改變。

We can describe the fate of a cell in such a way that the pluripotent cells are located on the top of a mountain and the underlying signaling network in cells is like a gravity that wants to pull the cell down to reach a differentiated state. So the challenge in cell reprogramming is twofold: not only to lift the differentiated cells to the top of the hill, but also to silence those factors that attract cell differentiation.
Cell reprogramming originally introduced OSKM into cells via retroviruses, but other combinations of transcription factors were also successful later on, suggesting that cellular reprogramming involves complex dynamic processes and state transitions. The iPSC generated by this method has high heterogeneity, which leads to cell mutation and low reprogramming efficiency. To use iPSC clinically, there are other ways to avoid retroviruses. (Extended reading: Nature published Shinya Yamanaka new results, iPS correction of circular chromosomes)
Because of this, a number of second-generation iPS approaches have been developed, some of which have shown better security. The reproducibility and simplicity of retroviruses make them still active in in vitro studies. However, in the field of regenerative medicine, episomal plasmid is more favored. Other methods include adenovirus, Sendai virus, synthetic protein and RNA. However, these methods, while more secure, have higher technical requirements and no improvement in reprogramming efficiency. Recent studies have shown that cell reprogramming can be accomplished with only small molecules. This means that indirect target molecular pathways associated with pluripotency are sufficient to regain the cell's fate.
Understanding the molecular pathways described above can help people to prevent cells that have entered the pluripotent state from returning to their differentiated state. Differences between DNA methylation and histone acetylation exist between pluripotent cells and differentiated cells. In addition, small molecules of the target epigenetic mechanism enhance reprogramming efficiency. In general, special attention needs to be paid to changes in epigenetic factors in the promotion of reprogramming efficiency.

Villin is a gastrointestinal-associated cytoskeletal protein associated with microfilament-like microvasculars on the brush border. In normal tissues, Villin is usually expressed only on brush border cells, such as gastrointestinal epithelial cells, pancreatic and biliary epithelial cells, and renal parenchymal epithelium (especially proximal tubules). Villin as a gut-specific reference, combined with CDX2, can be used for intestinal epithelial tumors and non-intestinal epithelial tumor research. Villin can also be used as a reference indicator for gastrointestinal neuroendocrine tumors.