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:
FLCN, BHD, FLCL

Immunogen: Recombinant fusion protein of human FLCN (NP_653207.1).

Swissprot: Q8NFG4
Gene ID: 201163

Purification Method: Affinity purification

Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3

Concentration: 1 mg/mL
Dilution: IF 1:50-1:100

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