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AIPL1 antibody

Anti-AIPL1 antibody used in IHC (Paraffin sections) (IHC-P). GTX17024
Anti-AIPL1 antibody used in IHC (Paraffin sections) (IHC-P). GTX17024
Anti-AIPL1 antibody used in Western Blot (WB). GTX17024

Cat. No. GTX17024

Host

 Rabbit

Clonality

 Polyclonal

Isotype

 IgG

Application

 WB, IHC-P, ELISA

Reactivity

 Human, Mouse
Package
100 μg ($399)
See all AIPL1 products

APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application Recommended Dilution
WB 1 - 2 μg/mL
IHC-P 2.5 μg/mL
ELISA Assay dependent
Not tested in other applications.

Calculated MW

44 kDa. ( Note )

Positive Control

Human Brain Tissue Slide(GTX22203) , Human Brain Tissue Lysate(GTX27918)

PROPERTIES

Form

Liquid

Buffer

PBS

Preservative

0.02% Sodium azide

Storage

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

Concentration

1 mg/ml (Please refer to the vial label for the specific concentration.)

Antigen Species

Human

Immunogen

Aipl1 antibody was raised against a 17 amino acid synthetic peptide near the carboxy terminus of the human Aipl1.The immunogen is located within amino acids 290 - 340 of Aipl1.

Purification

Purified by antigen-affinity chromatography

Conjugation

Unconjugated

Note

For laboratory research use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.

Purchasers shall not, and agree not to enable third parties to, analyze, copy, reverse engineer or otherwise attempt to determine the structure or sequence of the product.

TARGET

Synonyms

aryl hydrocarbon receptor interacting protein like 1 , AIPL2 , LCA4

Cellular Localization

Cytoplasm,Nucleus

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]

Database

Research Area

DATA IMAGES

Anti-AIPL1 antibody used in IHC (Paraffin sections) (IHC-P). GTX17024

GTX17024 IHC-P Image

IHC-P analysis of human brain tissue using GTX17024 AIPL1 antibody.
Working concentration : 20 μg/ml

Anti-AIPL1 antibody used in IHC (Paraffin sections) (IHC-P). GTX17024

GTX17024 IHC-P Image

IHC-P analysis of human brain tissue using GTX17024 AIPL1 antibody.
Working concentration : 2.5 μg/ml

Anti-AIPL1 antibody used in Western Blot (WB). GTX17024

GTX17024 WB Image

WB analysis of human brain tissue lysate using GTX17024 AIPL1 antibody.
Working concentration : (A) 1 and (B) 2 μg/ml

REFERENCE

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REVIEW

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SDS
PBS.pdf
Sodium Azide.pdf
Package List Price ($)
$ 399