AIPL1 (Human) Matched Antibody Pair

Catalog # H00023746-AP11

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Price

Stock

Quantity

Size:1 Set
Price: USD $ 607.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from 0.3 ng/ml to 100 ng/ml.

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human AIPL1.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (87); Rat (87)

    Quality Control Testing

    Standard curve using recombinant protein ( H00023746-P01 ) as an analyte.

    Sandwich ELISA detection sensitivity ranging from 0.3 ng/ml to 100 ng/ml.

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: rabbit MaxPab® affinity purified polyclonal anti-AIPL1 (100 ug)
    2. Detection antibody: mouse monoclonal anti-AIPL1, IgG2a Kappa (20 ug)
    *Reagents are sufficient for at least 1-2 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Recombinant protein)

  • Gene Info — AIPL1

    Entrez GeneID

    23746

    Gene Name

    AIPL1

    Gene Alias

    AIPL2, LCA4

    Gene Description

    aryl hydrocarbon receptor interacting protein-like 1

    Omim ID

    604392 604393

    Gene Ontology

    Hyperlink

    Gene Summary

    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

    Other Designations

    -

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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