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IFT80


Official Full Name
intraflagellar transport 80
Organism
Homo sapiens
Gene ID
57560
Background
The protein encoded by this gene is part of the intraflagellar transport complex B and is necessary for the function of motile and sensory cilia. Defects in this gene are a cause of asphyxiating thoracic dystrophy 2 (ATD2). Three transcript variants encoding two different isoforms have been found for this gene.[provided by RefSeq, Jun 2010]
Synonyms
ATD2; SRTD2; WDR56; FAP167; CFAP167

Cat.No. Product Name Price
SHH317353 shRNA set against Human IFT80 (NM_020800.2) Inquiry
SHH317357 shRNA set against Mouse IFT80 (NM_026641.2) Inquiry
SHH317361 shRNA set against Rat IFT80 (NM_001013911.1) Inquiry
SHL167574 shRNA set against Rat Ift80(NM_001013911.1) Inquiry
SHW007800 shRNA set against Danio rerio IFT80 (NM_001008625) Inquiry
Cat.No. Product Name Price
CDFR002990 Rat Ift80 cDNA Clone(NM_001013911.1) Inquiry
MiUTR1R-02595 IFT80 miRNA 3'UTR clone Inquiry
MiUTR3H-11690 IFT80 miRNA 3'UTR clone Inquiry
CDCB157727 Human IFT80 ORF clone (BC113669) Inquiry
CDCB169275 Danio rerio IFT80 ORF Clone (NM_001008625) Inquiry
CDCB188732 Rabbit IFT80 ORF clone (XM_002716337.2) Inquiry
CDCL119675 Human IFT80 ORF clone (NM_001190241.1) Inquiry
CDCR259041 Mouse Ift80 ORF Clone(NM_026641.2) Inquiry
CDCR305905 Human IFT80 ORF Clone(NM_020800.2) Inquiry
CDCR370067 Rat Ift80 ORF Clone(NM_001013911.1) Inquiry
CDCS418734 Human IFT80 ORF Clone (BC113669) Inquiry
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