FLCN

gene product
BHD, MGC17998, MGC23445
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, Jul 2008]
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37 antibodies from 15 providers.

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AntibodyRefsTypeWBELIFIPIHFC
Proteintech Group
1 antibody
GeneTex
3 antibodies
Aviva Systems Biology
4 antibodies
Bethyl Laboratories, Inc.
2 antibodies
Novus Biologicals
8 antibodies
Thermo Fisher Scientific Pierce
1 antibody
Atlas Antibodies
1 antibody
Abnova Corporation
3 antibodies
Acris Antibodies GmbH
4 antibodies
Epitomics
2 antibodies
Cell Signaling Technology, Inc
1 antibody
Santa Cruz Biotechnology
1 antibody
Sigma-Aldrich
2 antibodies
Abbiotec
1 antibody
antibodies-online
3 antibodies