CDH23 (Human) Recombinant Protein (Q01)

Catalog # H00064072-Q01

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Size:25 ug
Price: USD $ 510.00
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  • +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 CDH23 partial ORF ( NP_071407, 29 a.a. - 114 a.a.) recombinant protein with GST-tag at N-terminal.

    Sequence

    PFFTNHFFDTYLLISEDTPVGSSVTQLLAQDMDNDPLVFGVSGEEASRFFAVEPDTGVVWLRQPLDRETKSEFTVEFSVSDHQGVI

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    35.2

    Interspecies Antigen Sequence

    Mouse (95); Rat (96)

    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 — CDH23

    Entrez GeneID

    64072

    GeneBank Accession#

    NM_022124

    Protein Accession#

    NP_071407

    Gene Name

    CDH23

    Gene Alias

    DFNB12, DKFZp434P2350, FLJ00233, FLJ36499, KIAA1774, KIAA1812, MGC102761, USH1D

    Gene Description

    cadherin-like 23

    Omim ID

    601067 601386 605516

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is a large, single-pass transmembrane protein composed of an extracellular domain containing 27 repeats that show significant homology to the cadherin ectodomain. Expressed in the neurosensory epithelium, the protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Two alternative splice variants have been identified that encode different isoforms. Additional variants have been observed but their full-length nature has not been determined. [provided by RefSeq

    Other Designations

    OTTHUMP00000044780|cadherin 23|cadherin related 23|cadherin-23|otocadherin

  • 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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