中和抗体滴度检测试剂盒Neutralizing antibo
dy titer assay kit|印度突变株 Delta | B.1.617.2|Anti-SARS-CoV-2 (B.1.617.2) |Neutralizing Antibody Titer Serologic Assay Kit (Spike Trimer)- ￥6825
- ACROBiosystems
- RAS-N041
- USA
- 2026年01月16日
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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 库存：
现货
- 供应商：
ACROBiosystems
- 适应物种：
自收到试剂盒，2-8℃可保存12个月；重构后样品-70℃可保存1个月，建议开封后1个月内使用。
- 标记物：
2-8℃
- 样本：
Anti-SARS-CoV-2 (B.1.617.2) Neutralizing Antibody Titer Serologic Assay Kit (Spike Trimer)
- 规格：
96tests
Multiple variants of SARS-CoV-2 are circulating globally and posting new challenges to human health. As concerns over the potential impacts of the variants grow, people ask if one possesses protective neutralizing antibodies (NAbs) against the variants after receiving the currently available vaccines; and if the NAb therapeutic agents are equally effective to treat the mutant infection as the wild type. To facilitate the mutant-related research, drug trials and vaccine assessments, a high-throughput assay to measure neutralizing antibodies against the mutants is in urgent need.
Application
This kit is developed for qualitative detection or titer measurement of Anti-SARS-CoV-2 (B.1.617.2) neutralizing antibody (Spike Trimer) in human serum.Reconstitution
Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.Storage
The unopened kit is stable for 12 months from the date of manufacture if stored at 2°C to 8°C.风险提示：丁香通仅作为第三方平台，为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全，合理判断，谨慎选购商品，商家和用户对交易行为负责。对于医疗器械类产品，请先查证核实企业经营资质和医疗器械产品注册证情况。
- 作者
- 内容
- 询问日期
文献和实验Basic Protocol 1: Screening of Anti‐HCV Compounds in Hepatoma Cells Basic Protocol 2: Quantification of HCV Infection Using a Cell‐Based NS3 Protease Assay Support Protocol 1: Generation of HCVcc from In Vitro–
protein, hepatitis delta antigen (HDAg). The high affinity of HDAg for the HDV RNA genome, combined with the well-characterized anti-HDAg antibodies, made this system a logical starting point for the development of the RIP assay. Cells with replicating HDV
抗体，将样本中加入已结合了保护性抗原（PA）IgG和致死性因子(LF)IgG的微球，使其与anti—PA—IgG和anti—LF-IgG反应，通过分析micr0sphere—PA—IgG(-LF)-anti-IgG—R—phycoerythrin的平均荧光强度(MFIs)，实现对患者血清中两种炭疽杆菌毒素的定量分析。相应的研究还有对呼吸道合胞病毒和西尼罗河病毒以及与自身免疫性疾病有关的9种自身抗体(SS—A，SS—B，Sm，RNP，Scl-70，Jo-1，CENP-B，PribosomalanddsDNA
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