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- 详细信息
- 文献和实验
- 技术资料
- 保质期:
见COA
- 库存:
大量
- 供应商:
北京辰辉创聚生物技术有限公司
- 规格:
100ug; 500ug; 1mg; Bulk

| 产品信息
品名:NebuSelect™ Recombinant Canine F8/Coagulation factor VIII Protein, 2183-2341aa, His-tag
中文名称:重组犬F8, Coagulation factor VIII蛋白
别名:Coagulation factor VIII, Procoagulant component, F8
货号:NBL-300853
品牌:Nebulabio
规格:100UG;1MG;Bulk
| 产品描述
NebuSelect™ Recombinant Canine F8/Coagulation factor VIII Protein, His-tag (Cat# NBL-300853) is E. coli with His Tag. This recombinant protein is of high purity, verified to be greater than 90% by SDS-PAGE. Endotoxin levels are less than 1 EU/µg, as determined by the LAL (Limulus Amebocyte Lysate) assay.
| 产品属性
Species:Canis lupus familiaris
Expression System:E. coli
Molecular Weight:19 kDa
Target Name:Dog F8, Coagulation factor VIII
Purity:>90% by SDS-PAGE.
Formulation:See COA
Endotoxin:<1 EU/ug(LAL Method)
Storage:4°C for short term. -20°C for long term.
For Research Use Only!
To get more information, please contact us freely.
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文献和实验Identification of Mutations in the Human Factor VII Gene
It has been recognized from the early 1800s that activation of coagulation can be initiated by the exposure of subendothelial layers (tissue factor), but it was the 1940s before factor VII (FVII) was included in this event
Ex Vivo Stromal Cell Electroporation of Factor IX cDNA for Treatment of Hemophilia B
Hemophilia B is an X-linked genetic disorder that typically results from chronic circulating deficiency of blood coagulation factor IX (FIX) (1). While the occurrence of hemophilia B is significantly less frequent than hemophilia A (factor
Detection of Mutations in Hemophilia A Patients by Chemical Cleavage of Mismatch Method
Hemophilia A is an X-linked disorder that leads to a defect in blood coagulation. This is caused by mutations in the factor VIII gene, which results in its activity being reduced or abolished in the blood-clotting cascade. The factor VIII
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