TTC8 antibody
Principal name
TTC8 antibody
Alternative names for TTC8 antibody
Tetratricopeptide repeat domain 8 isoform CRA_, Putative uncharacterized protein TTC
SwissProt ID
A6NFG2 (Human)
Gene ID
123016 (TTC8)
Ncbi ID
Available reactivities
Available hosts
Available applications
Enzyme Immunoassay (E), Western blot / Immunoblot (WB), ELISA (detection) (E(detection))
Background of TTC8 antibody
This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. Alternate transcriptional splice variants have been characterized. [provided by RefSeq]. Transcript Variant: This variant (2) lacks an in-frame exon, compared to variant 1, resulting in a shorter protein (isoform B), as compared to isoform A.
