AIPL1 Blocking peptide
Product Sizes
100ug
£183.00
AAP96760-100UG
About this Product
- SKU:
- AAP96760
- Additional Names:
- LCA4; AIPL2
- Extra Details:
- Leber congenital amaurosis (LCA) is the most severe inherited retinopathy with the earliest age of onset and accounts for at least 5% of all inherited retinal diseases. Affected individuals are diagnosed at birth or in the first few months of life with nystagmus; severely impaired vision or blindness and an abnormal or flat electroretinogram. The photoreceptor/pineal-expressed gene; AIPL1; encoding aryl-hydrocarbon interacting protein-like 1; is located within the LCA4 candidate region. The encoded protein contains three tetratricopeptide motifs; consistent with chaperone or nuclear transport activity. Mutations in this gene may cause approximately 20% of recessive LCA. Alternative splicing results in multiple transcript variants.
- Gene Details:
- aryl hydrocarbon receptor interacting protein-like 1
- Shipping Conditions:
- Blue Ice
- Storage Conditions:
- Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage; store at -20C. Avoid repeat freeze-thaw cycles.
- Supplier:
- Aviva Systems Biology
- Type:
- Proteins, Peptides, Small Molecules & Other Biomolecules: Peptides
