Pages
Products

HYDIN


Official Full Name
HYDIN axonemal central pair apparatus protein
Organism
Homo sapiens
Gene ID
54768
Background
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]
Synonyms
CILD5; HYDIN1; HYDIN2; PPP1R31

Cat.No. Product Name Price
SHH137117 shRNA set against Mouse Hydin(NM_172916.2) Inquiry
SHH316217 shRNA set against Human HYDIN (NM_017558.4) Inquiry
SHH316221 shRNA set against Mouse HYDIN (NM_172916.2) Inquiry
SHW002887 shRNA set against Chicken HYDIN (NM_001159371) Inquiry
SHW012279 shRNA set against Danio rerio HYDIN (NM_001114415) Inquiry
Cat.No. Product Name Price
MiUTR1M-05866 HYDIN miRNA 3'UTR clone Inquiry
MiUTR3H-11485 HYDIN miRNA 3'UTR clone Inquiry
CDCB164362 Chicken HYDIN ORF Clone (NM_001159371) Inquiry
CDCB173754 Danio rerio HYDIN ORF Clone (NM_001114415) Inquiry
CDCB189427 Rabbit HYDIN ORF clone (XM_008257593.1) Inquiry
CDCL119059 Human HYDIN ORF clone (NM_001198543.1) Inquiry
CDCL119061 Mouse HYDIN ORF clone (NM_001198542.1) Inquiry
CDCS418720 Human HYDIN ORF Clone (BC028351) Inquiry
Quick Inquiry