TTC8 antibody, Internal,Genetex,GTX88117
Host
Goat
Reactivity
Human
Application
WB
Conjugate
Unconjugated
Platform ID
BAB831936325

Genetex
Contact
Tel: 1-949-553-1900
Fax: 1-949-309-2888
Email:
Specifications
Scientific Background
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]
Synonyms
tetratricopeptide repeat domain 8 , BBS8 , RP51
Category Paths
- Products>Primary Antibodies>Polyclonal Antibodies
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