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SNURF Protein (AA 1-71) (His tag)

SNURF Origin: Human Host: Escherichia coli (E. coli) Recombinant > 90 % by SDS - PAGE SDS
Catalog No. ABIN5853504
  • Target See all SNURF Proteins
    SNURF (SNRPN Upstream Reading Frame (SNURF))
    Protein Type
    Recombinant
    Protein Characteristics
    AA 1-71
    Origin
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Source
    • 4
    • 1
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This SNURF protein is labelled with His tag.
    Application
    SDS-PAGE (SDS)
    Sequence
    MGSSHHHHHH SSGLVPRGSH MGSMERARDR LHLRRTTEQH VPEVEVQVKR RRTASLSNQE CQLYPRRSQQ QQVPVVDFQA ELRQAFLAET PRGG
    Purity
    > 90 % by SDS - PAGE
    Top Product
    Discover our top product SNURF Protein
  • Application Notes
    Optimal working dilution should be determined by the investigator.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.25 mg/mL
    Buffer
    Liquid. In 20  mM Tris-HCl buffer (  pH 8.0) containing 0.15M NaCl, 40 % glycerol, 1  mM DTT.
    Storage
    4 °C,-20 °C,-80 °C
    Storage Comment
    Can be stored at +4C short term (1-2 weeks). For long term storage, aliquot and store at -20C or -70C. Avoid repeated freezing and thawing cycles.
  • Target
    SNURF (SNRPN Upstream Reading Frame (SNURF))
    Alternative Name
    SNuRF (SNURF Products)
    Synonyms
    2410045I01Rik Protein, Snrpn Protein, SNRPN upstream reading frame Protein, small nuclear ribonucleoprotein polypeptide N Protein, SNURF Protein, SNRPN Protein, Snurf Protein
    Background
    SNuRF is a highly basic protein localized to the nucleus. The evolutionarily constrained open reading frame is found on a bicistronic transcript which has a downstream ORF encoding the small nuclear ribonucleoprotein polypeptide N. The upstream coding region utilizes the first three exons of the transcript, a region that has been identified as an imprinting center. Multiple transcription initiation sites have been identified and extensive alternative splicing occurs in the 5' untranslated region but the full-length nature of these transcripts has not been determined. An alternate exon has been identified that substitutes for exon 4 and leads to a truncated, monocistronic transcript. Alternative splicing or deletion caused by a translocation event in the 5' uTR or coding region of this gene leads to Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure. The function of this protein is not yet known. Recombinant human SNuRF protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques.
    Molecular Weight
    10.8 kDa (94aa) confirmed by MALDI-TOF
    NCBI Accession
    NP_073715
    UniProt
    Q9Y675
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