ARG45985

anti-AIPL1 antibody

anti-AIPL1 antibody for Western blot,IHC-Formalin-fixed paraffin-embedded sections and Human,Mouse,Rat

Overview

Product Description Rabbit Polyclonal antibody recognizes AIPL1
Tested Reactivity Hu, Ms, Rat
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name AIPL1
Antigen Species Human
Immunogen A 18 amino acid synthetic peptide within aa. 140 - 190 of human AIPL1.
Conjugation Un-conjugated
Alternate Names aryl hydrocarbon receptor interacting protein-like 1; Aipl1; LCA4; AIPL2; Aryl-hydrocarbon-interacting protein-like 1

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-PAssay-dependent
WBAssay-dependent
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Purification Affinity chromatography purified
Buffer PBS and 0.02% Sodium azide.
Preservative 0.02% Sodium azide
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -35°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 114230 Mouse AIPL1

GeneID: 23746 Human AIPL1

GeneID: 59110 Rat AIPL1

Gene Symbol AIPL1
Gene Full Name aryl hydrocarbon receptor interacting protein-like 1
Background 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. [provided by RefSeq, Jan 2014]
Function May be important in protein trafficking and/or protein folding and stabilization. [UniProt]
Cellular Localization Cytoplasm; Nucleus. [UniProt]
Calculated MW 44 kDa