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FLCN
FolliculinBHD, DENND8B, 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]
Top validated antibodies |
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| NSJ Bioreagents |  RQ5662 |
Polyclonal |
WB
EL
ICC
IHC
FC
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| Boster Biological Technology | A00718-1 |
Polyclonal |
WB
EL
ICC
IHC
FC
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| Invitrogen Antibodies | 11236-2-AP |
Polyclonal |
WB
IP
IHC
OA
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| Proteintech Group | 11236-2-AP |
Polyclonal |
WB
EL
IP
IHC
|
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| Biorbyt | orb623858 |
Polyclonal |
WB
EL
ICC
IHC
FC
|
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