NNE protein (30R-AN007)
Purified nativeHuman NNE protein
Overview
Overview
| Synonyms | Non-Neuronal Enolase Protein |
|---|---|
| Species | Human |
| Protein Type | Native |
| Applications | User optimized |
Specifications
| Source | Human brain |
|---|---|
| Grade & Purity | > 60% pure |
| Method of Purification | NNE protein was purified using Ion-exchange chromatography and gel-filtration. |
| Form & Buffer | 10mM Tris-HCl, 5mM Mg2SO4, pH 7.5. |
| Concentration | Batch dependent - please inquire should you have specific requirements |
Storage & Safety
| Storage | Aliquot and store at -20 deg C. Avoid repeated Freeze/Thaw cycles |
|---|---|
| Biohazard Information | Donor samples were tested and found to be negative for HBsAg, HCV, HIV-1 and 2 antibodies, and syphilis. Nonetheless caution should be used when handling this material as there is a margin of error in all tests. |
General Information
| Biological Significance | Enolase, also known as phosphopyruvate dehydratase, is a metalloenzyme responsible for the catalysis of the conversion of 2-phosphoglycerate (2-PG) to phosphoenolpyruvate (PEP), the ninth and penultimate step of glycolysis. There are three subunits of enolase, a, ß, and , each encoded by a separate gene that can combine to form five different isoenzymes. Non-neuronal enolase is found ina variety of tissues including the liver, brian, kidney, and spleen. NNE is composed of two alpha enolase subunits. |
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