AIPL1 Antibody (N-term) Blocking peptide
€363.00
In stock
SKU
AC-BP12385a
Background:
Leber congenital amaurosis (LCA) accounts for at least 5%of all inherited retinal disease and is the most severe inheritedretinopathy with the earliest age of onset. Individuals affectedwith LCA are diagnosed at birth or in the first few months of lifewith severely impaired vision or blindness, nystagmus and anabnormal or flat electroretinogram. The photoreceptor/pineal-expressed gene, AIPL1, encoding aryl-hydrocarbon interactingprotein-like 1, was mapped within the LCA4 candidate region. Theprotein contains three tetratricopeptide motifs, consistent withnuclear transport or chaperone activity. AIPL1 mutations may causeapproximately 20% of recessive LCA.
Other Names:
Aryl-hydrocarbon-interacting protein-like 1, AIPL1, AIPL2
Gene Name: AIPL1
Gene ID: 23746
Primary Accession: Q9NZN9
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
Leber congenital amaurosis (LCA) accounts for at least 5%of all inherited retinal disease and is the most severe inheritedretinopathy with the earliest age of onset. Individuals affectedwith LCA are diagnosed at birth or in the first few months of lifewith severely impaired vision or blindness, nystagmus and anabnormal or flat electroretinogram. The photoreceptor/pineal-expressed gene, AIPL1, encoding aryl-hydrocarbon interactingprotein-like 1, was mapped within the LCA4 candidate region. Theprotein contains three tetratricopeptide motifs, consistent withnuclear transport or chaperone activity. AIPL1 mutations may causeapproximately 20% of recessive LCA.
Other Names:
Aryl-hydrocarbon-interacting protein-like 1, AIPL1, AIPL2
Gene Name: AIPL1
Gene ID: 23746
Primary Accession: Q9NZN9
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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