AIPL1 antibody

Catalog No. ABIN2715813

The Mouse Monoclonal anti-AIPL1 antibody has been validated for WB, IF and FACS. It is suitable to detect AIPL1 in samples from Human.

Quick Overview for AIPL1 antibody (ABIN2715813)

Target: AIPL1 (Aryl Hydrocarbon Receptor Interacting Protein-Like 1 (AIPL1))

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This AIPL1 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone: 1B2

Product Details anti-AIPL1 Antibody

Characteristics: Homo sapiens aryl hydrocarbon receptor interacting protein-like 1 (AIPL1), transcript variant 1

Purification: Purified from mouse ascites fluids by affinity chromatography

Immunogen: Full length human recombinant protein of human AIPL1(NP_055151) produced in HEK293T cell.

Isotype: IgG1

Application Details

Application Notes: WB 1:2000, IF 1:100, FLOW 1:100,

Comment:

The concentration of the product may vary between diferrent lots.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5-1.0 mg/mL

Buffer: PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Target Details for AIPL1

Target: AIPL1 (Aryl Hydrocarbon Receptor Interacting Protein-Like 1 (AIPL1))

Alternative Name: AIPL1

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.

Molecular Weight: 43.7 kDa

Gene ID: 23746

NCBI Accession: NM_014336

HGNC: 23746