ADAMTS10 (Human) Recombinant Protein

Catalog # P3798

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Size:10 ug
Price: USD $ 308.00
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  • Specification

    Product Description

    Human ADAMTS10 (NP_001101.1, 214 a.a. - 672 a.a.) partial recombinant protein expressed in Escherichia coli.

    Sequence

    TTSAEKNTCQLYIQTDHLFFKYYGTREAVIAQISSHVKAIDTIYQTTDFSGIRNISFMVKRIRINTTADEKDPTNPFRFPNIGVEKFLELNSEQNHDDYCLAYVFTDRDFDDGVLGLAWVGAPSGSSGGICEKSKLYSDGKKKSLNTGIITVQNYGSHVPPKVSHITFAHEVGHNFGSPHDSGTECTPGESKNLGQKENGNYIMYARATSGDKLNNNKFSLCSIRNISQVLEKKRNNCFVESGQPICGNGMVEQGEECDCGYSDQCKDECCFDANQPEGRKCKLKPGKQCSPSQGPCCTAQCAFKSKSEKCRDDSDCAREGICNGFTALCPASDPKPNFTDCNRHTQVCINGQCAGSICEKYGLEECTCASSDGKDDKELCHVCCMKKMDPSTCASTGSVQWSRHFSGRTITLQPGSPCNDFRGYCDVFMRCRLVDADGPLARLKKAIFSPELYENIAE

    Host

    Escherichia coli

    Form

    Liquid

    Preparation Method

    Escherichia coli expression system

    Purity

    > 95% by SDS-PAGE

    Quality Control Testing

    10% SDS-PAGE Result

    Storage Buffer

    In PBS (50% glycerol)

    Storage Instruction

    Store at -20°C. For long term storage store at -80°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    SDS-PAGE

  • Gene Info — ADAMTS10

    Entrez GeneID

    81794

    Protein Accession#

    NP_001101.1

    Gene Name

    ADAMTS10

    Gene Alias

    ADAM-TS10, WMS

    Gene Description

    ADAM metallopeptidase with thrombospondin type 1 motif, 10

    Omim ID

    277600 608990

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene belongs to the ADAMTS (a disintegrin and metalloproteinase domain with thrombospondin type-1 motifs) family of zinc-dependent proteases. ADAMTS proteases are complex secreted enzymes containing a prometalloprotease domain of the reprolysin type attached to an ancillary domain with a highly conserved structure that includes at least one thrombospondin type 1 repeat. They have been demonstrated to have important roles in connective tissue organization, coagulation, inflammation, arthritis, angiogenesis and cell migration. The product of this gene plays a major role in growth and in skin, lens, and heart development. It is also a candidate gene for autosomal recessive Weill-Marchesani syndrome. [provided by RefSeq

    Other Designations

    Weill-Marchesani syndrome|a disintegrin and metalloproteinase with thrombospondin motifs 10|a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 10|a disintegrin-like and metalloprotease domain with thrombospondin typ

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