MYO15A monoclonal antibody (M01), clone 7F2

Catalog # H00051168-M01

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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 MYO15A is 3 ng/ml as a capture antibody.

QC Test

Western Blot detection against Immunogen (36.63 KDa) .

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a partial recombinant MYO15A.

    Immunogen

    MYO15A (NP_057323.2, 3432 a.a. ~ 3530 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    PCILAINHNGLNFLSTETHELMVKFPLKEIQSTRTQRPTANSSYPYVEIALGDVAAQRTLQLQLEQGLELCRVVAVHVENLLSAHEKRLTLPPSEITLL

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (87)

    Isotype

    IgG2a Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (36.63 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 MYO15A is 3 ng/ml as a capture antibody.

    ELISA

  • Gene Info — MYO15A

    Entrez GeneID

    51168

    GeneBank Accession#

    NM_016239

    Protein Accession#

    NP_057323.2

    Gene Name

    MYO15A

    Gene Alias

    DFNB3, DKFZp686N18198, FLJ17274, FLJ31311, MYO15

    Gene Description

    myosin XVA

    Omim ID

    600316 602666

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene have been associated with profound, congenital, neurosensory, nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified, but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described, but their full length sequences have not been determined. [provided by RefSeq

    Other Designations

    myosin XV|unconventional myosin-15

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