SNURF 抗体 (Middle Region)
This anti-SNURF antibody is a 兔 多克隆 antibody detecting SNURF in WB 和 EIA. Suitable for 人.
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Quick Overview for SNURF 抗体 (Middle Region) (ABIN357983)
抗原
See all SNURF 抗体
SNURF
(SNRPN Upstream Reading Frame (SNURF))
适用
人
宿主
兔
克隆类型
多克隆
标记
This SNURF antibody is un-conjugated
应用范围
Western Blotting (WB), Enzyme Immunoassay (EIA)
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抗原表位
- Middle Region
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特异性
- This antibody detects SNURF (Center).
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纯化方法
- Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
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免疫原
- This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the Center region of human SNURF.
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亚型
- Ig Fraction
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anti-SNRPN Upstream Reading Frame (SNURF) (AA 1-240) antibody
SNURF 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
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应用备注
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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
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS with 0.09 % (W/V) Sodium Azide as preservative.
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储存液
- Sodium azide
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注意事项
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.
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- SNURF (SNRPN Upstream Reading Frame (SNURF))
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别名
- SNURF
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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
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分子量
- 8412 Da (Theoretical pI: 10.58. WB band detected at approx 30kDa).
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基因ID
- 8926, 9606
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UniProt
- Q9Y675
抗原
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