AIPL1 蛋白
(Aryl Hydrocarbon Receptor Interacting Protein-Like 1 (AIPL1))
Leber congenital amaurosis (LCA) accounts for at least 5% of all inherited retinal disease and is the most severe inherited retinopathy with the earliest age of onset. Individuals affected with LCA are diagnosed at birth or in the first few months of life with severely impaired vision or blindness, nystagmus and an abnormal or flat electroretinogram. The photoreceptor/pineal -expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, was mapped within the LCA4 candidate region. The protein contains three tetratricopeptide motifs, consistent with nuclear transport or chaperone activity. AIPL1 mutations may cause approximately 20% of recessive LCA. [provided by RefSeq, Jul 2008].
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12 results
custom-made
AIPL1
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
AIPL1
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
AIPL1
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for AIPL1 蛋白
aryl hydrocarbon receptor interacting protein like 1 (AIPL1) 蛋白aryl hydrocarbon receptor interacting protein like 1 (aipl1) 蛋白
aryl hydrocarbon receptor-interacting protein-like 1 (Aipl1) 蛋白
A930007I01Rik 蛋白
AIPL1 蛋白
aipl2 蛋白
AIPL2 蛋白
lca4 蛋白
LCA4 蛋白
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