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SNURF 抗体 (Middle Region)

SNURF 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN357983
发货至: 中国
  • 抗原 See all SNURF 抗体
    SNURF (SNRPN Upstream Reading Frame (SNURF))
    抗原表位
    • 2
    • 1
    • 1
    • 1
    • 1
    Middle Region
    适用
    宿主
    • 3
    • 2
    克隆类型
    • 5
    多克隆
    标记
    • 5
    This SNURF antibody is un-conjugated
    应用范围
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB), Enzyme Immunoassay (EIA)
    特异性
    This antibody detects SNURF (Center).
    纯化方法
    Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
    免疫原
    This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the Center region of human SNURF.
    亚型
    Ig Fraction
    Top Product
    Discover our top product SNURF Primary Antibody
  • 应用备注
    ELISA: 1/1,000. Western Blot: 1/50-1/100.
    Other applications not tested.
    Optimal dilutions are dependent on conditions and should be determined by the user.
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    0.25 mg/mL
    缓冲液
    PBS with 0.09 % (W/V) Sodium Azide as preservative.
    储存液
    Sodium azide
    注意事项
    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    注意事项
    Avoid repeated freezing and thawing.
    储存条件
    4 °C/-20 °C
    储存方法
    Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
  • 抗原
    SNURF (SNRPN Upstream Reading Frame (SNURF))
    别名
    SNURF (SNURF 产品)
    别名
    2410045I01Rik antibody, Snrpn antibody, SNRPN upstream reading frame antibody, small nuclear ribonucleoprotein polypeptide N antibody, SNURF antibody, SNRPN antibody, Snurf antibody
    背景
    SNURF is a highly basic protein localized to the nucleus. The evolutionarily constrained open reading frame of its gene 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.Synonyms: SNRPN upstream reading frame protein
    分子量
    8412 Da (Theoretical pI: 10.58. WB band detected at approx 30kDa).
    基因ID
    8926, 9606
    UniProt
    Q9Y675
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