MYO7A (Human) Recombinant Protein (Q01)

Catalog # H00004647-Q01

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Size:25 ug
Price: USD $ 510.00
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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
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  • Specification

    Product Description

    Human MYO7A partial ORF ( NP_000251, 2118 a.a. - 2213 a.a.) recombinant protein with GST-tag at N-terminal.

    Sequence

    KQTTEPNFPEILLIAINKYGVSLIDPKTKDILTTHPFTKISNWSSGNTYFHITIGNLVRGSKLLCETSLGYKMDDLLTSYISQMLTAMSKQRGSRS

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    36.3

    Interspecies Antigen Sequence

    Mouse (98); Rat (97)

    Preparation Method

    in vitro wheat germ expression system

    Purification

    Glutathione Sepharose 4 Fast Flow

    Quality Control Testing

    12.5% SDS-PAGE Stained with Coomassie Blue.

    Storage Buffer

    50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

    Note

    Best use within three months from the date of receipt of this protein.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

    Western Blot (Recombinant protein)

    Antibody Production

    Protein Array

  • Gene Info — MYO7A

    Entrez GeneID

    4647

    GeneBank Accession#

    NM_000260

    Protein Accession#

    NP_000251

    Gene Name

    MYO7A

    Gene Alias

    DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B

    Gene Description

    myosin VIIA

    Omim ID

    276900 276903 600060 601317

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq

    Other Designations

    deafness, autosomal dominant 11|deafness, autosomal recessive 2|myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))

  • 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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