Recommended Products
shipped in
wet ice
storage temp.
2-8°C
General description
Kit is designed to remove all enterokinase (as judged by antigenic or enzymatic activity assays). This is accomplished by binding with immobilized rabbit antibodies to calf intestine enterokinase followed by spin filtration.
Application
For removal of enterokinase by immunoaffinity from fusion protein cleavage reaction mixtures. 100 μl of a 50% slurry of the anti-enterokinase-agarose can remove at least 7 μg of bovine enterokinase or 1 μg of recombinant catalytic subunit.
Preparation Note
Dilute required amount of 20X Wash Buffer 1:20 in distilled water.
Kit Components Only
Product No.
Description
- 20× Wash buffer 4 mL
- Disposable spin filters 10 ea
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Information
新产品
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Ai Maekawa et al.
Journal of hypertension, 27(1), 181-189 (2009-01-17)
Prostasin, a glycosylphosphatidylinositol-anchored serine protease, regulates epithelial sodium channel (ENaC) activity. Sodium reabsorption through ENaC in distal nephron segments is a rate-limiting step in transepithelial sodium transport. Recently, proteolytic cleavage of ENaC subunits by prostasin has been shown to activate
Mary Harpen et al.
Journal of virology, 83(21), 10869-10876 (2009-08-28)
As obligatory parasites, viruses co-opt a variety of cellular functions for robust replication. The expression of the nonsegmented negative-strand RNA genome of respiratory syncytial virus (RSV), a significant pediatric pathogen, absolutely requires actin and is stimulated by the actin-regulatory protein
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service