• Product NameRecombinant Human FLCN
• Brief DescriptionRecombinant Protein
• Immunogen DescriptionFusion protein corresponding to C terminal 250 amino acids of human folliculin
• Target Namefolliculin
• Alternative Names    BHD; FLCL
• Accession No. Swissprot:Q8NFG4
  Gene Accession:NP_659434
• UniprotQ8NFG4
• Gene ID201163;
• Storage -20~-80˚C, pH 7.6 PBS

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.

Note: For in vitro research use only, not for diagnostic or therapeutic use. This product is not a medical device.

• Flow Cytometry (FCM) General Protocol
• Immunofluorescence(IC)
• Immunohistochemistry(Polymer)
• Western Blotting