SNURF 抗体 (AA 4-32)
SNURF
适用: 人
宿主: 兔
Polyclonal
RB17346
unconjugated
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- 抗原 See all SNURF 抗体
- SNURF (SNRPN Upstream Reading Frame (SNURF))
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抗原表位
- AA 4-32
- 适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This SNURF antibody is un-conjugated
- 应用范围
- 请咨询
- 预测反应
- B, M, Rb
- 纯化方法
- This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
- 免疫原
- This SNURF antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 4-32 amino acids from the Central region of human SNURF.
- 克隆位点
- RB17346
- 亚型
- Ig Fraction
- Top Product
- Discover our top product SNURF Primary Antibody
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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
anti-SNRPN Upstream Reading Frame (SNURF) (Middle Region) antibodySNURF 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated
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- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 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.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
- 有效期
- 6 months
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- 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.
- 分子量
- 8412
- 基因ID
- 8926
- NCBI登录号
- NP_005669, NP_073715
- UniProt
- Q9Y675
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