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SMNDC1 Protein (Myc-DYKDDDDK Tag)

SMNDC1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2732252
  • Target See all SMNDC1 Proteins
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    Protein Type
    Recombinant
    Origin
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 4
    • 1
    • 1
    • 1
    HEK-293 Cells
    Purification tag / Conjugate
    This SMNDC1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human SMNDC1 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 SMNDC1 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
    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))
    Alternative Name
    Smndc1 (SMNDC1 Products)
    Synonyms
    smnr Protein, spf30 Protein, SMNDC1 Protein, SMNR Protein, SPF30 Protein, TDRD16C Protein, wu:fb37h07 Protein, wu:fc23a07 Protein, 2410004J23Rik Protein, 4933440I19Rik Protein, survival motor neuron domain containing 1 Protein, smndc1 Protein, SMNDC1 Protein, Bm1_41545 Protein, Smndc1 Protein
    Background
    This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.
    Molecular Weight
    26.5 kDa
    NCBI Accession
    NP_005862
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