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- 详细信息
- 文献和实验
- 技术资料
- 亚型:
IgG1
- 形态:
Liquid
- 保存条件:
at-20℃
- 适应物种:
Human
- 库存:
99
- 宿主:
Mouse
- 应用范围:
FCM
- 浓度:
见说明
- 抗体英文名:
Anti-Human HLA-G Monoclonal antibody (33342#)
- 规格:
50-100ug
小鼠抗人HLA-G单克隆抗体(克隆号33342#)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.

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文献和实验Isolation of Resident Cardiac Progenitor Cells by Hoechst 33342 Staining
of stem cells to efficiently efflux vital dyes such as Hoechst 33342. During fluoresence activated cell sorting (FACS) such Hoechst-extruding cells appear to the side of Hoechst-dye retaining cells and have thus been termed side population (SP) cells
1.悬浮生长的细胞在培养状态下加入Heochst 33342,终浓度为1μg/ml;帖壁生长的细胞用含有0.02%EDTA的0.25%胰蛋白酶消化成单细胞悬液,离心,弃上清,用1ml全培养液重悬细胞,加入Heochst 33342,终浓度为1μg/ml,37℃孵育7~10min。 2.4℃ 500~1000r/min离心弃去染液。 3.加入1.0ml PI染液,4℃避光染色15min。 4.400目的筛网过滤1次。 5.流式细胞仪分析。
双苯咪唑类的Hochest-33342和33258及 JC-1染色
双苯咪唑类的Hochest-33342和33258及 JC-1染色 双苯咪唑类的Hochest-33342和33258 该染料可渗透细胞 膜进入细胞内,与DNA结合,使之染色。凋亡细胞对该染料的摄取增高,染色后呈强蓝色荧光。其实验方法如下。 (1)细胞培养及凋亡的诱导:将细胞接种在10cm的培养皿中(106 细胞),在适当的时机诱导细胞凋亡。 (2)收集细胞:悬浮生长的细胞
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