TEV Protease
![mRNA synthesis](/media/diy/images/page/figure1-mrna.png)
mRNA synthesis
In vitro transcription of capped mRNA with modified nucleotides and Poly(A) tail
![Tyramine Signal Amplification (TSA)](/media/diy/images/page/figure2-01.png)
Tyramide Signal Amplification (TSA)
TSA (Tyramide Signal Amplification), used for signal amplification of ISH, IHC and IC etc.
![screening library](/media/diy/images/page/figure3-01.png)
Phos Binding Reagent Acrylamide
Separation of phosphorylated and non-phosphorylated proteins without phospho-specific antibody
![Cell Counting Kit-8 (CCK-8)](/media/diy/images/page/CCK-8.jpg)
Cell Counting Kit-8 (CCK-8)
A convenient and sensitive way for cell proliferation assay and cytotoxicity assay
![SYBR Safe DNA Gel Stain](/media/diy/images/page/SYBR Safe DNA Gel Stain.png)
SYBR Safe DNA Gel Stain
Safe and sensitive stain for visualization of DNA or RNA in agarose or acrylamide gels.
![Inhibitor Cocktails](/media/diy/images/page/Inhibitor Cocktails.jpg)
Inhibitor Cocktails
Protect the integrity of proteins from multiple proteases and phosphatases for different applications.
TEV蛋白酶是一种具有最高催化效率的高度特异性半胱氨酸蛋白酶。其识别序列为ENLYFQ ▼S,但P1'位置的氨基酸也可以是G、A、M、C或H(1)。TEV蛋白酶通常用于从融合蛋白中去除亲和纯化标签,例如用于去除融合蛋白的Glutathione S-transferase (GST)、His或者其它标签的蛋白酶。TEV蛋白酶具有His标签,可从使用镍亲和树脂的反应中轻松去除,所以适用于带His标签的融合蛋白的酶切反应,而没有完全酶切的带His标签的重组蛋白、切除下来的His标签以及TEV Protease (His-tag)都可以经镍柱结合的方式除去,最终得到的流穿液(Flow-through)中含有所需的靶蛋白。在实际操作过程中,为尽量保留目的蛋白的结构和生物活性,建议在4℃用TEV Protease酶切过夜。TEV Protease在pH6.0-9.0范围内具有活性,而当pH小于或等于5时,会降低甚至失去酶活性。
Component | 1000 U | 5000 U | 10000 U |
TEV Protease | 0.1 ml | 0.5 ml | 1 ml |
10X TEV Protease Reaction Buffer | 1 ml | 1 ml x5 | 1 ml x10 |
Long-term storage: -20 °C |