FGF13 (Human) Recombinant Protein

Catalog # P8612

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Price

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Quantity

Size:25 ug
Price: USD $ 216.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Human FGF13 recombinant protein expressed in Escherichia coli.

    Sequence

    MAAAIASSLIRQKRQAREREKSNACKCVSSPSKGKTSCDKNKLNVFSRVKLFGSKKRRRRRPEPQLKGIVTKLYSRQGYHLQLQADGTIDGTKDEDSTYTLFNLIPVGLRVVAIQGVQTKLYLAMNSEGYLYTSELFTPECKFKESVFENYYVTYSSMIYRQQQSGRGWYLGLNKEGEIMKGNHVKKNKPAAHFLPKPLKVAMYKEPSLHDLTEFSRSGSGTPTKSRSVSGVLNGGKSMSHNEST

    Host

    Escherichia coli

    Theoretical MW (kDa)

    27.6

    Form

    Lyophilized

    Preparation Method

    Escherichia coli expression system

    Purification

    chromatography

    Surface Modification

    Greater than 95.0% as determined by:(a) Analysis by RP-HPLC.(b) Analysis by SDS-PAGE.

    Storage Buffer

    Lyophilized from a solution containing 20mM PB, 0.5M NaCl, pH 7.4. Reconstitute the lyophilized powder in ddH2O to 100 ug/mL.

    Storage Instruction

    Lyophilized protein at room temperature for 3 weeks, should be stored at -20°C. Protein aliquots at 4°C for 2-7 days and should be stored at -20°C to -80°C. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).
    Avoid repeated freeze/thaw cycles.

  • Applications

    SDS-PAGE

  • Gene Info — FGF13

    Entrez GeneID

    2258

    Protein Accession#

    Q92913

    Gene Name

    FGF13

    Gene Alias

    FGF2, FHF2

    Gene Description

    fibroblast growth factor 13

    Omim ID

    300070

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. This gene is located in a region on chromosome X, which is associated with Borjeson-Forssman-Lehmann syndrome (BFLS), making it a possible candidate gene for familial cases of the BFLS, and for other syndromal and nonspecific forms of X-linked mental retardation mapping to this region. Alternative splicing of this gene at the 5' end results in several transcript variants encoding different isoforms with different N-termini. [provided by RefSeq

    Other Designations

    OTTHUMP00000024143|OTTHUMP00000024144|fibroblast growth factor homologous factor 2

  • Interactome
  • Pathway
  • 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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