AIPL1 Mouse Monoclonal Antibody [Clone ID: LBI1B2]
Product Specifications
Background
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]
Synonyms
AIPL2; LCA4
Gene Name
Aryl hydrocarbon receptor interacting protein like 1
Gene ID
23746
UniProt
Q9NZN9
Conjugation
Unconjugated
Concentration
0.47 mg/ml
Dilution
WB 1:2000, IF 1:100, FLOW 1:100
Form
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Buffer
PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Function
Druggable Genome
Storage Conditions
Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
Symbol
AIPL1
Overview
AIPL1 mouse monoclonal antibody, clone LBI1B2
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/?term=23746
Uniprot URL
https://www.uniprot.org/uniprot/Q9NZN9
Curated Selection
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