TTC8 抗体
(Tetratricopeptide Repeat Domain 8 (TTC8))
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, Jul 2008].
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37 results
TTC8
适用: 人, 小鼠, 大鼠
WB, FACS, IF (cc), IF (p)
宿主: 兔
Polyclonal
AbBy Fluor® 350
Latest Publications for our TTC8 抗体
: "BBS4 and BBS5 show functional redundancy in the BBSome to regulate the degradative sorting of ciliary sensory receptors." in: Scientific reports, Vol. 5, pp. 11855, (2015) (PubMed).: "Essential role of the chaperonin CCT in rod outer segment biogenesis." in: Investigative ophthalmology & visual science, Vol. 55, Issue 6, pp. 3775-85, (2014) (PubMed).
: "The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSome." in: PLoS genetics, Vol. 10, Issue 2, pp. e1004083, (2014) (PubMed).
: "BBS mutations modify phenotypic expression of CEP290-related ciliopathies." in: Human molecular genetics, Vol. 23, Issue 1, pp. 40-51, (2013) (PubMed).
: "BBS7 and TTC8 (BBS8) mutations play a minor role in the mutational load of Bardet-Biedl syndrome in a multiethnic population." in: Human mutation, Vol. 30, Issue 7, pp. E737-46, (2009) (PubMed).
Aliases for TTC8 抗体
tetratricopeptide repeat domain 8 (TTC8) 抗体tetratricopeptide repeat domain 8 (ttc8) 抗体
tetratricopeptide repeat domain 8 (lpa_01174) 抗体
tetratricopeptide repeat domain 8 (Ttc8) 抗体
0610012F22Rik 抗体
AV001447 抗体
bbs8 抗体
BBS8 抗体
DKFZp459L2429 抗体
fk26c02 抗体
RP51 抗体
TTC8 抗体
wu:fk26c02 抗体
zgc:136718 抗体
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