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Recombinant Human SerpinE1/PAI-1 Protein (His Tag)

Recombinant Human SerpinE1/PAI-1 Protein (His Tag)
  • Recombinant Human SerpinE1/PAI-1 Protein (His Tag)
  • Recombinant Human SerpinE1/PAI-1 Protein (His Tag)

Price: ¥3600.00 ¥1200.00

Size:
100 μg 20 μg
  • 表达系统: HEK293 Cells
  • 蛋白编码: P05121
别称
Endothelial Plasminogen Activator Inhibitor;PAI;PAI-1;PAI1;PLANH1;Plasminogen Activator Inhibitor 1;SERPINE1;Serpin E1
表达系统
HEK293 Cells
序列
Val24-Pro402
蛋白编码
P05121
种属
Human
计算分子量
43.8 kDa
表观分子量
48 kDa
标签
C-His
生物活性
Not validated for activity
纯度
> 95% as determined by reducing SDS-PAGE.
内毒素
< 1.0 EU/mg of the protein as determined by the LAL method
保存条件
Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80℃. Reconstituted protein solution can be stored at 4-8℃ for 2-7 days. Aliquots of reconstituted samples are stable at < -20℃ for 3 months.
运输条件
This product is provided as lyophilized powder which is shipped with ice packs.
制剂
Lyophilized from a 0.2 μm filtered solution in PBS with 5% Trehalose and 5% Mannitol.
复溶方法
It is recommended that sterile water be added to the vial to prepare a stock solution of 0.5 mg/mL. Concentration is measured by UV-Vis.
背景
Serpins are a group of proteins with similar structures that were first identified as a set of proteins able to inhibit proteases. They are the largest and most diverse family of serine protease inhibitors which are involved in a number of fundamental biological processes such as blood coagulation, complement activation, fibrinolysis, angiogenesis, inflammation and tumor suppression and are expressed in a cell-specific manner. Serpin E1 is a secreted protein which belongs to the Serpin family. Serpin E1 acts as 'bait' for tissue plasminogen activator, urokinase, and protein C. Its rapid interaction with TPA may function as a major control point in the regulation of fibrinolysis. Defects in SERPINE1 are characterized by abnormal bleeding due to Serpin E1 defect in the plasma. High concentrations of Serpin E1 have been associated with thrombophilia which is an autosomal dominant disorder in which affected individuals are prone to develop serious spontaneous thrombosis.
> 95 % as determined by reducing SDS-PAGE.


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