Learn More
Description
The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq
Specifications
Specifications
| Antigen | PSPH |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 3A5 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full-length recombinant PSPH. |
| Formulation | ascites with no preservative |
| Gene | PSPH |
| Gene Accession No. | BC063614 |
| Gene Alias | PSP |
| 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.