- ￥2210 - 23040
- Solarbio
- P00273
- 北京
- 2025年07月25日
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￥988
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
现询
- 供应商：
北京索莱宝科技有限公司
- 规格：
1mg/500ug/50ug
| 规格： | 1mg | 产品价格： | ￥23040.0 |
|---|---|---|---|
| 规格： | 500ug | 产品价格： | ￥15360.0 |
| 规格： | 50ug | 产品价格： | ￥2210.0 |
| 基本信息 | |
| 基因名 | |
| 外观(性状) | Supplied as a 0.2 μM filtered solution of PBS, PH7.4. |
| 纯度 | ≥95% as determined by reducing SDS-PAGE. |
| 储存条件 | Reconstituted protein solution should be stored at ≤ -20°C.Stable for at least 24 months when stored as instructed. |
| 运输条件 | The product is shipped at 2-8°C temperature. Upon receipt, store it immediately at the temperature listed below. |
| 背景说明 | Protein S (PROS1) is glycoprotein and expressed in many cell types supporting its reported involvement in multiple biological processes that include coagulation，apoptosis，cancer development and progression，and the innate immune response.Known receptors bind S1 are ACE2，angiotensin-converting enzyme 2，DPP4，CEACAM etc.The spike (S) glycoprotein of coronaviruses is known to be essential in the binding of the virus to the host cell at the advent of the infection process.Most notable is severe acute respiratory syndrome (SARS).The severe acute respiratory syndrome-coronavirus (SARS-CoV) spike (S) glycoprotein alone can mediate the membrane fusion required for virus entry and cell fusion.It is also a major immunogen and a target for entry inhibitors.It's been reported that 2019-nCoV can infect the human respiratory epithelial cells through interaction with the human ACE2 receptor.The spike protein is a large type I transmembrane protein containing two subunits，S1 and S2.S1 mainly contains a receptor binding domain (RBD)，which is responsible for recognizing the cell surface receptor.S2 contains basic elements needed for the membrane fusion.The S protein plays key parts in the induction of neutralizing-antibody and T-cell responses，as well as protective immunity. |
| 单位 | 支 |
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文献和实验Combined 3C-ChIP-Cloning (6C) Assay: A Tool to Unravel Protein-Mediated Genome Architecture
between chromatin elements without specifically identifying the protein components that mediate such interactions. Here we describe a detailed protocol for C ombined 3C -C hIP-C loning (6C) technology, which combines multiple techniques to identify the proteins
Structural and Functional Analysis of the HCV p7 Protein
intervention to combat viral hepatitis C infection. In this context, in vitro functional analyses of isolated p7 coupled to structural characterization are critical for further understanding of the molecular mechanisms of p7 ion-channel activity
Production of Recombinant Antibodies in Drosophila melanogaster S2 Cells
One of the major bottlenecks in antibody discovery for research and therapeutic applications is the need for large quantities of protein in a short amount of time. Here we describe an alternative method using the Drosophila melanogaster S2
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