重组SARS E蛋白(Coronavirus) (ab48949)
Key features and details
- Expression system: Escherichia coli
- Purity: > 90% SDS-PAGE
- Active: Yes
- Tags: His tag C-Terminus
- Suitable for: ELISA, WB
描述
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产品名称
重组SARS E蛋白(Coronavirus) -
生物活性
Immunoreactive with sera from SARS-infected individuals.
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纯度
> 90 % SDS-PAGE. -
表达系统
Escherichia coli -
蛋白长度
Protein fragment -
无动物成分
No -
性质
Recombinant -
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氨基酸
1 to 76 -
标签
His tag C-Terminus -
额外的序列信息
E protein immunodominant region.
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技术指标
Our Abpromise guarantee covers the use of ab48949 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
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应用
ELISA
Western blot
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形式
Liquid -
Concentration information loading...
制备和贮存
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稳定性和存储
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -80°C. Avoid freeze / thaw cycle.
pH: 7.2
Constituent: PBSThis product is an active protein and may elicit a biological response in vivo, handle with caution.
常规信息
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别名
- E protein
- Envelope protein
- Envelope small membrane protein
see all -
相关性
A novel coronavirus has recently been identified as the causative agent of SARS (Severe Acute Respiratory Syndrome). Coronaviruses are a major cause of upper respiratory diseases in humans. The genomes of these viruses are positive stranded RNA approximately 27 to 31kb in length. SARS infection can be mediated by the binding of the viral spike protein, a glycosylated 139 kDa protein and the major surface antigen of the virus, to the angiotensin converting enzyme 2 (ACE2) on target cells. This binding can be blocked by a soluble form of ACE2. The evelope protein is a component of the viral envelope that plays a central role in virus morphogenesis and assembly. It may be sufficient to form virus like particles. -
细胞定位
Cell Membrane; single pass membrane protein.
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
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Datasheet download
文献 (0)
ab48949 尚未被引用在任何文献中。