Learn More
STK11 Rabbit anti-Human, Polyclonal Antibody, Abnova™
Description
This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterized by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterized. [provided by RefSeq
Specifications
Specifications
| Antigen | STK11 |
| Applications | ELISA, Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Rabbit polyclonal antibody raised against synthetic peptide of STK11. |
| Dilution | Western blot (5 to 10 ug/mL) The optimal working dilution should be determined by the end user. |
| Formulation | In PBS, pH 7.4 |
| Gene | STK11 |
| Gene Alias | LKB1/PJS |
| Gene Symbols | STK11 |
| Show More |
For Research Use Only
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.