TTC8 antibody, Internal

GeneTex

TTC8 antibody, Internal

10

Western Blot

Research Use Only

Polyclonal

0.50 mg/ml

Goat

IgG

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. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

Human

2°C to 8°C,-20°C

12352203