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Recombinant Human AIPL1, His-tagged

Cat.No.: AIPL1-9509H
Product Overview: Recombinant Human AIPL1 protein, fused to His-tag, was expressed in E.coli and purified by Ni-sepharose.
Description: 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.
Source: E.coli
Species: Human
Tag: His
Protein length: C-term-355a.a.
Storage: The protein is stored in PBS buffer at -20℃. Avoid repeated freezing and thawing cycles.
Storage Buffer: 1M PBS (58mM Na2HPO4,17mM NaH2PO4, 68mM NaCl, pH8. ) added with 300mM Imidazole and 0.7% Sarcosyl, 15%glycerol.
Gene Name: AIPL1 aryl hydrocarbon receptor interacting protein-like 1 [ Homo sapiens ]
Official Symbol: AIPL1
Synonyms: AIPL1; aryl hydrocarbon receptor interacting protein-like 1; aryl hydrocarbon receptor interacting protein like 1 , LCA4; aryl-hydrocarbon-interacting protein-like 1; LCA4; AIPL2;
Gene ID: 23746
mRNA Refseq: NM_001033054
Protein Refseq: NP_001028226
MIM: 604392
UniProt ID: Q9NZN9
Chromosome Location: 17p13.1
Function: binding; farnesylated protein binding; unfolded protein binding;

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