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RS1 Protein (Myc-DYKDDDDK Tag)

RS1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2730763
  • Target See all RS1 Proteins
    RS1 (Retinoschisin 1 (RS1))
    Protein Type
    Recombinant
    Origin
    • 3
    • 1
    Human
    Source
    • 2
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This RS1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human Retinoschisin / RS1 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 RS1 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
    RS1 (Retinoschisin 1 (RS1))
    Alternative Name
    Retinoschisin,rs1 (RS1 Products)
    Synonyms
    RS Protein, XLRS1 Protein, Rs1h Protein, Xlrs1 Protein, tmgc1 Protein, rs1 Protein, zgc:92703 Protein, retinoschisin 1 Protein, retinoschisin 1 S homeolog Protein, retinoschisis (X-linked, juvenile) 1 (human) Protein, retinoschisin 1a Protein, RS1 Protein, rs1.S Protein, rs1 Protein, Rs1 Protein, rs1a Protein
    Background
    This gene encodes an extracellular protein that plays a crucial role in the cellular organization of the retina. The encoded protein is assembled and secreted from photoreceptors and bipolar cells as a homo-oligomeric protein complex. Mutations in this gene are responsible for X-linked retinoschisis, a common, early-onset macular degeneration in males that results in a splitting of the inner layers of the retina and severe loss in vision.
    Molecular Weight
    23 kDa
    NCBI Accession
    NP_000321
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