FLCN Polyclonal Antibody

Background:
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.

Research Area: Cancer

Synonyms:
BHD, BHD skin lesion fibrofolliculoma protein, Birt Hogg Dube syndrome protein, Birt-Hogg-Dube syndrome protein, DKFZp547A118, FLCL, Flcn, FLCN, FLJ45004, FLJ99377, Folliculin, MGC17998, MGC23445

Immunogen: Recombinant protein of human FLCN

Swissprot: Q8NFG4
Gene Accession: NP_659434

Purification Method: Affinity purification

Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4

Concentration: 0.2 mg/mL
Dilution: IHC 1:100-1:300

Storage:
Store at -20°C. Avoid freeze / thaw cycles.

Alternative for product with catalog number:
sc-25168/sc-25777