OTOA monoclonal antibody (M03), clone 1F5

Catalog # H00146183-M03

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Size:100 ug
Price: USD $ 335.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Sandwich ELISA (Recombinant protein)
Application

Sandwich ELISA (Recombinant protein)

Detection limit for recombinant GST tagged OTOA is 0.03 ng/ml as a capture antibody.

QC Test

Western Blot detection against Immunogen (36.52 KDa) .

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a partial recombinant OTOA.

    Immunogen

    OTOA (NP_653273.3, 27 a.a. ~ 124 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    NSRQDLHPLLQNMAEEIIDGSYLNALLDLIQFQSSHVWTDDLSHRVLAYLNSRNVAFTIPSLQAAVENHLEQRLHQPQKLLEDLRKTDAQQFRTAMKC

    Host

    Mouse

    Reactivity

    Human

    Isotype

    IgG2a Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (36.52 KDa) .

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Recombinant protein)

    Sandwich ELISA (Recombinant protein)

    Detection limit for recombinant GST tagged OTOA is 0.03 ng/ml as a capture antibody.

    ELISA

  • Gene Info — OTOA

    Entrez GeneID

    146183

    GeneBank Accession#

    NM_144672

    Protein Accession#

    NP_653273.3

    Gene Name

    OTOA

    Gene Alias

    DFNB22, FLJ32773, MGC157747, MGC39813

    Gene Description

    otoancorin

    Omim ID

    607038 607039

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is specifically expressed in the inner ear, and is located at the interface between the apical surface of the inner ear sensory epithelia and their overlying acellular gels. It is prposed that this protein is involved in the attachment of the inner ear acellular gels to the apical surface of the underlying nonsensory cells. Mutations in this gene are associated with autosomal recessive deafness type 22 (DFNB22). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [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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