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IFT43
Intraflagellar transport 43C14orf179, FLJ32173, MGC16028
This gene encodes a subunit of the intraflagellar transport complex A (IFT-A). IFT-A is a multiprotein complex that plays an important role in cilia assembly and maintenance by mediating retrograde ciliary transport. Mutations in this gene are a cause of cranioectodermal dysplasia-3 (CED3), also known as Sensenbrenner syndrome. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Top validated antibodies |
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| Atlas Antibodies |  HPA003438 |
1 references | Polyclonal |
WB
ICC
IHC
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| Novus Biologicals | NBP1-92019 |
1 references | Polyclonal |
WB
ICC
IHC
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| Proteintech Group | 24338-1-AP |
5 references | Polyclonal |
EL
IHC
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| NovoPro Bioscience Inc. | 133091 |
Polyclonal |
WB
EL
IHC
FC
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| antibodies-online | ABIN2840304 |
Polyclonal |
WB
IHC
FC
|
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