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- ProSci
- 美国
- PSI-36-106-100ug
- 2025年07月15日
- E, Func, ICC, IHC, IP, WB
- 小鼠
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant human LAG-3.
- 保存条件：
Stable for at least 1 year after receipt when stored at -20℃
- 保质期：
1年
- 级别：
科研级别
- 库存：
100
- 供应商：
艾美捷科技
- 宿主：
小鼠
- 应用范围：
E, Func, ICC, IHC, IP, WB
- 抗体英文名：
LAG-3 Antibody [11E3] (preservative free)
- 抗体名：
LAG-3 Antibody [11E3] (preservative free)
- 规格：
100ug
LAG-3 抗体 [11E3] (preservative free)，LAG-3 Antibody [11E3] (preservative free)，LAG-3 抗体 [11E3] (preservative free),LAG-3 Antibody [11E3] (preservative free)
产品名称：LAG-3 抗体 [11E3] (preservative free)-LAG-3 Antibody [11E3] (preservative free)
产品货号：PSI-36-106-100ug
产品规格：100ug
背景资料：Lymphocyte activation gene 3 (LAG-3; CD223) plays an important role in negatively regulating T cell proliferation, function and homeostasis. It is required for maximal natural and induced regulatory T cell (Treg) function. LAG-3 is closely related to the T cell co-receptor CD4 and binds to MHC class II molecules but with a significantly higher affinity than CD4.
保存建议：LAG-3 抗体 [11E3] (preservative free)-LAG-3 Antibody [11E3] (preservative free)Stable for at least 1 year after receipt when stored at -20℃
应用类型：E, Func, ICC, IHC, IP, WB
点击：LAG-3 抗体 [11E3] (preservative free)-LAG-3 Antibody [11E3] (preservative free)查看更详细产品说明，更多应用、储存、价格、货期等信息请垂询艾美捷科技有限公司。更多ProSci公司特色试剂盒、特色抗体以及特色试剂等产品评论，请点击查看艾美捷特色产品中心。
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文献和实验Use of DNA Combing to Study DNA Replicationin Xenopus and Human Cell-Free Systems
early development. To this end we adapted the DNA combing technique to investigate the distribution of replication bubbles along single DNA molecules. DNA replicating in egg extracts is labelled by addition of digoxigenin-11-dUTP and/or biotin-16-dUTP
monoclonal antibody production fusion
^6 cells/ml (IMDM + 10% FCS/FBS). Just before the fusion wash 3 times in IMDM (serum free!), 1200 rpm, 5min, 37ѓC. Count cells. sacrifice the mouse and dissect the spleen. tease the spleen in ice-cold IMDM (serum free!); pass
with digoxigenin are bound to the 3′ OH DNA ends by reacting with the TdT enzyme in ultrathin sections on a nickel grid. After incubation with an anti-digoxigenin antibody conjugated with 10-nm colloidal gold, the sections are then stained with uranyl acetate
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