ROR2 monoclonal antibody (M04), clone 4B8

Catalog # H00004920-M04

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Size:100 ug
Price: USD $ 335.00
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  • +1-909-264-1399
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  • +1-909-992-3401
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Sandwich ELISA (Recombinant protein)
Application

Sandwich ELISA (Recombinant protein)

Detection limit for recombinant GST tagged ROR2 is approximately 3ng/ml as a capture antibody.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against a partial recombinant ROR2.

    Immunogen

    ROR2 (NP_004551, 34 a.a. ~ 143 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.

    Sequence

    EVEVLDPNDPLGPLDGQDGPIPTLKGYFLNFLEPVNNITIVQGQTAILHCKVAGNPPPNVRWLKNDAPVVQEPRRIIIRKTEYGSRLRIQDLDTTDTGYYQCVATNGMKT

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (88); Rat (89)

    Isotype

    IgG2b Kappa

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

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

  • Applications

    Sandwich ELISA (Recombinant protein)

    Detection limit for recombinant GST tagged ROR2 is approximately 3ng/ml as a capture antibody.

    ELISA

  • Gene Info — ROR2

    Entrez GeneID

    4920

    GeneBank Accession#

    NM_004560

    Protein Accession#

    NP_004551

    Gene Name

    ROR2

    Gene Alias

    BDB, BDB1, MGC163394, NTRKR2

    Gene Description

    receptor tyrosine kinase-like orphan receptor 2

    Omim ID

    113000 268310 602337

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq

    Other Designations

    OTTHUMP00000021634|OTTHUMP00000063680|neurotrophic tyrosine kinase receptor-related 2|tyrosine-protein kinase transmembrane receptor ROR2

  • 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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