Learn More
Description
This gene is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in this gene are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of this gene results in two transcript variants encoding different isoforms. [provided by RefSeq
Specifications
Specifications
| Antigen | FLCN |
| Applications | ELISA, Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Mouse polyclonal antibody raised against a partial recombinant FLCN. |
| Formulation | 50% glycerol |
| Gene | FLCN |
| Gene Accession No. | NM_144606 |
| Gene Alias | BHD/DKFZp547A118/FLCL/FLJ45004/FLJ99377/MGC17998/MGC23445 |
| Gene Symbols | FLCN |
| 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.