ADAMTS2 (Human) Recombinant Protein (Q01)

Catalog # H00009509-Q01

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Size:25 ug
Price: USD $ 510.00
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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 ADAMTS2 partial ORF ( NP_055059, 1112 a.a. - 1210 a.a.) recombinant protein with GST-tag at N-terminal.

    Sequence

    KHNDIDVFMPTLPVPTVAMEVRPSPSTPLEVPLNASSTNATEDHPETNAVDEPYKIHGLEDEVQPPNLIPRRPSPYEKTRNQRIQELIDEMRKKEMLGK

    Host

    Wheat Germ (in vitro)

    Theoretical MW (kDa)

    36.63

    Interspecies Antigen Sequence

    Mouse (88); Rat (85)

    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 — ADAMTS2

    Entrez GeneID

    9509

    GeneBank Accession#

    NM_014244

    Protein Accession#

    NP_055059

    Gene Name

    ADAMTS2

    Gene Alias

    ADAM-TS2, ADAMTS-3, NPI, PCINP, PCPNI, hPCPNI

    Gene Description

    ADAM metallopeptidase with thrombospondin type 1 motif, 2

    Omim ID

    225410 604539

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene excises the N-propeptide of type I, type II and type V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in two transcript variants. The short transcript encodes a protein which has no significant procollagen N-peptidase activity. [provided by RefSeq

    Other Designations

    a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 2|procollagen I N-proteinase|procollagen N-endopeptidase

  • 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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