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百日咳毒素PTX,Pertussis Toxin

簡要描述:百日咳毒素是由細菌Bordetella pertussis產(chǎn)生的,以蛋白質(zhì)為基礎的AB5型外毒素。是特定靶向G蛋白抑制G蛋白及其在信號通路中的生理功能,在傳染方面發(fā)揮重要作用;還能在鼠類動物中刺激建立實驗性自身免疫疾病模型。

  • 產(chǎn)品型號:abs42024900
  • 廠商性質(zhì):生產(chǎn)廠家
  • 更新時間:2024-07-09
  • 訪  問  量:3728

詳細介紹

品牌absinCAS70323-44-3
分子式-純度>99%
分子量-貨號abs42024900
規(guī)格50ug供貨周期現(xiàn)貨
主要用途特定靶向G蛋白抑制G蛋白及其在信號通路中的生理功能應用領域醫(yī)療衛(wèi)生,環(huán)保,化工,生物產(chǎn)業(yè),農(nóng)業(yè)
產(chǎn)品描述
描述

Pertussis Toxin (islet-activating protein), a toxin originally isolated from Bordetella pertussis, has been shown to catalyze ADP-ribosylation of a protein in membrane preparation from rat C6 glioma cells. In addition, exposure of Chinese hamster ovary cells in culture to this compound has resulted in a clustered growth pattern response. Other experiments have shown Pertussis Toxin to block the ability of inhibitory hormones to reduce adenylate cyclase activity and enhance the ability of stimulatory hormones to activate the enzyme. Mechanistic studies have shown this toxin to consist of subunit A (active) promoter, which disrupts transmembrane signaling by ADP-ribosylating eukaryotic G-proteins, and B (binding) oligomer which helps the toxin bind to cells in vivo.

應用
A toxin that blocks reduction of adenylate cyclase activity
純度
>99%
活性
Please note that this product is not activated. If your system requires activation, see Kaslow et al.,for suggested conditions.
使用方法
CHO Cell Assay: When examined in a CHO cell assay as described by Hewlett et al.,5 the lowest concentration of toxin at which a positive response (clustered growth pattern) was obtained was 0.01 ng/ml.

Adenylate Cyclase Assay: The adenylate cyclase activity of this lot is 0.67 picomole/min/lJg in the presence of 1 μmolar calmodulin when assayed by the method of Wolff et al6
儲存/保存方法
This product is provided as an aseptically packaged lyophilized powder, sealed under vacuum. Store at 4°C prior to and following reconstitution, for 6 months. DO NOT FREEZE.
基本信息
外觀
Lyophilized solid
可溶性/溶解性
Soluble in water (Miscible). Reconstitute with sterile purified water or the sterile buffer of your choice. The resulting suspension should be made uniform by gentle mixing prior to use. Do not sterile filter, as this will result in loss of material. For long term storage, reconstitute in a high ionic strength buffer, such as sterile 0.1 M sodium phosphate, pH 7.0, 0.5 M NaCI. Handle the product gently; do not vortex.
參考文獻
參考文獻
1. Bradford, M.M. (1976) Anal. Biochem. 72, 248-254.
2. Tamura, M., Nogomori, K., Murai, S., Yajima, M., Ito, K" Katada, T., Ui, M. and Ishi, S. (1982) Biochem. 21,5516-5522.
3. Wyckoff, M., Rodbard, O. And Chramback, A. (1977) Anal. Biochem.78, 459-482.
4. Laemmli, U.K. (1970) Nature 227, 680-685.
5. Hewlett, E.L., Sauer, K.T., Myers, G.A., Cowell, J.L. and Guerrant, R.L. (1983) Infect. Immun. 40, 1198-1203.
6. Wolff, J., Cook, G.H., Goldhammer, A.R. and Berkowitz, S.A. (1980) PNAS 77, 3841-3844.
7. Kaslow, H.R., Lim, L.-K., Moss, J. and Lesikar, D.O. (1987) Biochem. 26, 123-127.

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