AIPL1 Mouse Monoclonal Antibody [Kloon ID: LBI3B4]

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]

Carrier-free (BSA/glycerol-free) AIPL1 mouse monoclonal antibody, clone LBI3B4

AIPL2; LCA4

Homo sapiens aryl hydrocarbon receptor interacting protein like 1 (AIPL1), transcript variant 1, mRNA.

23746

Q9NZN9

Unconjugated

WB 1:500~2000, IHC 1:150, IF 1:100, FLOW 1:100

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Druggable Genome

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable 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.

AIPL1

https://www.ncbi.nlm.nih.gov/gene/?term=23746

https://www.uniprot.org/uniprot/Q9NZN9