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The antibody against AIPL1 was raised in rabbit using the Recombinant Human Aryl-hydrocarbon-interacting protein-like 1 protein (1-384AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.
The antibody against AIPL1 was raised in rabbit using the Recombinant Human Aryl-hydrocarbon-interacting protein-like 1 protein (1-384AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, WB, IHC.
$299.00
| Cat.No | ADC-44221A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | AIPL1 |
| Form | Liquid | Species Reactivity | Human, Rat |
| Isotype | IgG | Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, IHC, WB | Storage | Upon receipt |
| Immunogen Description | Recombinant Human Aryl-hydrocarbon-interacting protein-like 1 protein (1-384AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q9NZN9 |
Uniprot Id
Q9NZN9
Target Species
Human
Target Name
AIPL1
Target Full Name
Aryl-hydrocarbon-interacting protein-like 1
Target Function
May be important in protein trafficking and/or protein folding and stabilization.
Target Involvement
Leber congenital amaurosis 4 (LCA4)
Target Subcellular Location
Cytoplasm. Nucleus.
Target Tissue Specificity
Highly expressed in retina. Specifically localized to the developing photoreceptor layer and within the photoreceptors of the adult retina.
Target Research Area
Signal Transduction
Target Synonyms
A930007I01Rik; Aipl1; AIPL1_HUMAN; AIPL2; Aryl hydrocarbon interacting protein like 1; Aryl hydrocarbon receptor interacting protein like 1; Aryl-hydrocarbon-interacting protein-like 1; LCA4; MGC25485; OTTHUMP00000128207; OTTMUSP00000006382; RP23-401C17.1
Target 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.
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