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Oligophrenin 1 Protein (OPHN1) (Myc-DYKDDDDK Tag)

OPHN1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2727904
  • Target See all Oligophrenin 1 (OPHN1) Proteins
    Oligophrenin 1 (OPHN1)
    Protein Type
    Recombinant
    Origin
    • 3
    • 2
    • 1
    Human
    Source
    • 2
    • 2
    • 2
    HEK-293 Cells
    Purification tag / Conjugate
    This Oligophrenin 1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Oligophrenin-1 protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product OPHN1 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    Oligophrenin 1 (OPHN1)
    Alternative Name
    Oligophrenin-1 (OPHN1 Products)
    Synonyms
    ARHGAP41 Protein, MRX60 Protein, OPN1 Protein, C130037N19Rik Protein, Opn1 Protein, MGC68856 Protein, zgc:92603 Protein, OPHN1 Protein, mrx60 Protein, opn1 Protein, oligophrenin 1 Protein, oligophrenin 1 L homeolog Protein, OPHN1 Protein, Ophn1 Protein, ophn1.L Protein, ophn1 Protein, Tsp_13482 Protein
    Background
    This gene encodes a Rho-GTPase-activating protein that promotes GTP hydrolysis of Rho subfamily members. Rho proteins are important mediators of intracellular signal transduction, which affects cell migration and cell morphogenesis. Mutations in this gene are responsible for OPHN1-related X-linked mental retardation with cerebellar hypoplasia and distinctive facial dysmorhphism.
    Molecular Weight
    91.5 kDa
    NCBI Accession
    NP_002538
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