missing translation for 'onlineSavingsMsg'
Läs mer
Läs mer
Description
The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content.
Specifications
Specifications
| Antigen | GYS2 |
| Användningsområden | Immunoprecipitation, Western Blot, Immunohistochemistry (Paraffin) |
| Klassificering | Polyclonal |
| Koncentration | 0.53 mg/mL |
| Konjugera | Unconjugated |
| Formulering | PBS with 50% glycerol and 0.02% sodium azide; pH 7.3 |
| Gen | GYS2 |
| Genaccessionsnr. | P17625, P54840, Q8VCB3 |
| Gene Alias | glycogen synthase 2 (liver), GYS2 |
| Gensymboler | Gys2 |
| Show More |
Product Title
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.
Spot an opportunity for improvement?