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Rabbit polyclonal AIPL1 antibody (A6458)
Supplier: ABclonal Inc.
Recommended applications: WB,IHC,IF
WB 1:500 – 1:2000 IHC 1:50 – 1:200 IF 1:50 – 1:100
Recommended protocols: check protocols
Click or hover above images to see image description for Rabbit polyclonal AIPL1 antibody.
Check alternative names for the antibodyExpand
LCA4 antibody, AIPL2 antibody
A930007I01Rik antibody|Aipl1 antibody|AIPL1_HUMAN antibody|AIPL2 antibody|Aryl hydrocarbon interacting protein like 1 antibody|Aryl hydrocarbon receptor interacting protein like 1 antibody|Aryl-hydrocarbon-interacting protein-like 1 antibody|LCA4 antibody|MGC25485 antibody|OTTHUMP00000128207 antibody|OTTMUSP00000006382 antibody|RP23-401C17.1 antibody|Anti-AIPL1 antibody (ab79044)
SCBT cat No: sc-134253|sc-46718|
Rabbit polyclonal AIPL1 antibody
|Catalogue No.|| |
Recombinant protein of human AIPL1
WB, IHC, IF
|Recommended dilution|| |
WB 1:500 – 1:2000
|Molecular weight|| |
Predicted: 43kDa/Observed: Refer to Figures
AIPL1 antibody was tube-contained.
AIPL1 antibody was purified using affinity purification.
Store at -20 Celsius degree. Avoid freeze / thaw cycles.
|Alternative antibody names|| |
LCA4 antibody, AIPL2 antibody
|Database links|| |
|Protein names|| |
|Protein function|| |
May be important in protein trafficking and/or protein folding and stabilization.
|Protein tissue specificity|| |
Highly expressed in retina. Specifically localized to the developing photoreceptor layer and within the photoreceptors of the adult retina.
|Protein sequence and domain|| |
Contains 1 PPIase FKBP-type domain.; Contains 3 TPR repeats.
|Protein cellular localization|| |
Cytoplasm . Nucleus .
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.
AntibodyPlus can customize AIPL1 antibody according to your requirement, including bulk product size,etc. Please contact email@example.com. AntibodyPlus provides antibody trial sample for your own antibody validation.
|Product type|| |
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