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- 详细信息
- 文献和实验
- 技术资料
- 抗体名:
InVivoMAb Anti-SARS-CoV-2 S2/Spike glycoprotein 2 Antibody (18H2)
- 抗体英文名:
InVivoMAb Anti-SARS-CoV-2 S2/Spike glycoprotein 2 Antibody (18H2)
- 浓度:
1 mg/ml
- 应用范围:
ELISA, Neutralization
- 宿主:
Mouse
- 保质期:
1 year
- 级别:
科研级
- 库存:
999
- 供应商:
AntibodySystem
- 克隆性:
Monoclonal
- 亚型:
IgG2a, kappa
- 规格:
100ug

| 宿主 | Mouse |
| 种属反应性 | SARS-CoV-2 (2019-nCoV) |
| 状态 | Liquid |
| 保存溶液 | 0.01M PBS, pH 7.4. |
| 浓度 | 1 mg/ml |
| 纯度 | >95% as determined by SDS-PAGE. |
| 克隆类型 | Monoclonal |
| 同种型 | IgG2a, kappa |
| 应用 | ELISA, Neutralization |
| 靶标 | Spike glycoprotein, S glycoprotein, Spike protein S2, S, 2, SARS-CoV-2 (2019-nCoV) |
| 纯化方式 | Protein A/G purified from cell culture supernatant. |
| 内毒素水平 | Please contact with the lab for this information. |
| Accession号 | P0DTC2 |
| 稳定性和存储 | Use a manual defrost freezer and avoid repeated freeze-thaw cycles. Store at 4°C short term (1-2 weeks). Store at -20°C 12 months. Store at -80°C long term. |
| 克隆号 | 18H2 |
| 备注 | For research use only. Not suitable for clinical or therapeutic use. |
Our products are designed for various research areas, supporting studies on 48 types of viruses, superbugs, parasites, cancer, Alzheimer's disease, Parkinson's disease, allergic responses, immune suppression, and immune activation.
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文献和实验中科院高福院士课题组 2020 年发表了哪些重要的研究成果?
抗体的主要靶标。2020 年 3 月 11 日,高福院士联合逯光文在 Cell Host & Microbe 发文:Structural Analysis of Rabies Virus Glycoprotein Reveals pH-Dependent Conformational Changes and Interactions with a Neutralizing Antibody。该研究报告了狂犬病毒 RABV-G 的晶体结构,分别在〜pH-8.0 时以游离形式和在〜pH-6.5 时与中和
5位院士为代表,超12篇CNS大作,5月新冠研究汇总——全方位围攻新冠病毒,值得收藏
的鸡尾酒疗法也引起了大家的关注,不同的抗体可以识别结合域上不同的抗原表位,在未来的临床应用中能够避免免疫逃逸的理想单克隆抗体对。 5 月 8 日,军事医学科学院生物工程研究所陈薇院士团队和西湖大学周强团队强强联合,在预印本平台 bioRxiv 上线题为:A potent neutralizing human antibody reveals the N-terminal domain of the Spike protein of SARS-CoV-2 as a site
Hematopoietic Stem Cell Targeting with Surface-Engineered Lentiviral Vectors
. 16. Wash the transduced cells and resuspend in CellGro medium. Incubate for 48 h. Determine transduction efficiency by analyzing enhanced GFP expression by flow cytometry after immunolabeling the cells with an anti-hCD34-PE antibody.
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