Tissue expression
Cell line expression
Protein structure
HYDIN
HYDIN axonemal central pair apparatus proteinCILD5, DKFZp434D0513, KIAA1864, PPP1R31
This gene encodes a protein that may be involved in cilia motility. Mutations in this gene cause of autosomal recessive primary ciliary dyskinesia-5, a disorder characterized by the accumulation of cerebrospinal fluid within the ventricles of the brain. A duplicate copy of this gene has been found in humans on chromosome 1. [provided by RefSeq, Jan 2013]
Top validated antibodies |
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NovoPro Bioscience Inc. | 111579 | Polyclonal |
WB
EL
IHC
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FineTest Biotech | FNab04091 | Polyclonal |
WB
EL
IHC
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Biorbyt | orb184271 | Polyclonal |
EL
ICC
IHC
|
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Invitrogen Antibodies | 24741-1-AP | Polyclonal |
WB
IHC |
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Atlas Antibodies | HPA067155 | Polyclonal |
IHC
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Supportive data in Antibodypedia
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Recommended by provider
Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider