Learn More
Description
The enzyme system for cleavage of glycine (glycine cleavage system; EC 2.1.2.10), which is confined to the mitochondria, is composed of 4 protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase; MIM 238300), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme; MIM 238310), and L protein (a lipoamide dehydrogenase; MIM 238331). Glycine encephalopathy (GCE; MIM 605899), also called nonketotic hyperglycinemia (NKH), may be due to a defect in any one of these enzymes.[supplied by OMIM
Specifications
Specifications
| Antigen | GCSH |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | M2 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full length recombinant GCSH. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | GCSH |
| Gene Accession No. | BC000790 |
| Gene Alias | GCE/NKH |
| Show More |
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.