SNURF antibody, Internal-多抗-深圳欣博盛生物科技有限公司

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SNURF antibody, Internal

品牌：GeneTex

官网链接

说明书

折扣/货期

货号：GTX82489

规格：400μl

目录价：￥5600

产品详情

* 以下信息仅供参考，详情请以原厂网站为准

产品名称:

SNURF antibody, Internal

别名:

SNRPN upstream reading frame

反应种属:

Human

宿主来源:

Rabbit

实验应用:

IHC-P

同种型:

IgG

免疫原:

KLH conjugated synthetic peptide between 4-32 amino acids from the Central region of human SNURF.

克隆性:

Polyclonal

克隆号:

纯化方式:

Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

偶联:

Unconjugated

产品浓度:

Batch dependent (Please refer to the vial label for the specific concentration.)

保存温度:

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

运输温度:

4°C

产品形式:

Liquid

存储溶液:

PBS, 0.09% Sodium azide.

生产商:

GeneTex

功能与背景:

This gene is located within the Prader-Willi Syndrome critical region on chromosome 15. Transcripts produced from this gene initiate at an imprinting center and are paternally-imprinted. These transcripts may be bicistronic and also encode SNRPN (small nuclear ribonucleoprotein polypeptide N) from a downstream open reading frame. The small protein represented by this gene is encoded by an evolutionarily-conserved upstream open reading frame and is localized to the nucleus. Extensive alternative splicing and promoter usage occurs in this region and the full-length nature of some of these transcripts has not been determined. Alterations in the imprinting center are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]

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