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- 保存条件：
at-20℃
- 库存：
99
- 抗体英文名：
Anti-Eimeria tenella Microneme protein Monoclonal antibody (1A149)
- 规格：
50-100ug
小鼠抗Eimeria tenella Microneme protein单克隆抗体(克隆号1A149)上海圻明生物优势供应欢迎咨询。配对抗体小课堂：
Paired antibodies are two antibodies that can bind to an antigenic molecule at the same time. Specifically:
Paired antibodies are commonly used in sandwich ELISA experiments
An antigenic molecule usually has multiple epitopes, and different antibodies can target different epitopes
When two antibodies are able to bind to different epitopes of the same antigenic molecule at the same time, the two antibodies are called paired antibodies
However, not all antibodies against different epitopes can be paired antibodies. Sometimes, when an antibody binds to an antigen, it may cause the configuration of other binding sites to change, making it impossible for other antibodies to bind properly
Steric hindrance effects may also result in two antibodies with close binding sites not being able to bind to the antigen at the same time
Therefore, the preparation of paired antibodies usually requires two steps: first the antibody is prepared, and then the paired antibody is screened
Screening of paired antibodies is typically performed using a sandwich ELISA method of bispecific antibodies, in which different combinations of antibodies are tested to determine which antibodies can be successfully paired
Paired antibodies have important applications in immunology research and diagnostics, especially in assays that require high specificity and sensitivity.
小鼠抗Eimeria tenella Microneme protein单克隆抗体(克隆号1A149)更多优势产品欢迎新老客户选购。
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MAB1600 小鼠抗ASFV I10L单克隆抗体(克隆号1A016)
MAB1601 小鼠抗ASFV NS4A单克隆抗体(克隆号1A017)
MAB1602 小鼠抗ASFV NS4A单克隆抗体(克隆号1A018)
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文献和实验许多靶标的超敏感检测。一、新的BL/CL生物技术工具新的BL/CL报告基因报告基因技术代表了分子生物学最近主要的进展之一。报告基因是一段DNA序列，编码一个很容易被侦测到的蛋白或酶。它们可以人工引入到一个细胞内来监测基因的表达，以得到整体细胞生物传感器或细胞定位的作用。报告基因技术应用到研发BL/CL全细胞生物传感器的原理如图1a。目前，细菌荧光素酶基因（如陆上的Photorhabdus luminescens和海洋中Vibrio harveyi细菌的lux基因），真核的来自于萤火虫Photinus
化。例如：缺少任何一种甲基转移酶对小鼠胚胎的发育都是致死性的（Li等1992年和Okano等1999年）[3]。此外，等位基因的抑制(allelic repression)被印记控制区(imprinting control regions, ICRs)所调控,该区域在双亲中的一个等位基因是甲基化的[4]。印记基因的异常表达可以引发伴有突变和表型缺陷的多种人类疾病。如：脐疝-巨舌-巨大发育综合征(Beckwith-Wiedemann Syndrome, BWS)和Prader-Willi
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