Human LGR5/GPR49, InVivo Block
/Neutralizing Antibody-Human LGR5/GPR49, InVivo Block/Neutralizing Antibody- 询价
- Biogradetech
- 美国
- BGT-ANT-37380
- 2025年07月14日
- ELISA,In vivo Neutralization
- Mouse
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
免疫原详情见datasheet，该抗体亚型为：IgG2a, kappa
- 保存条件：
-2°C-8°C
- 保质期：
1年
- 库存：
100
- 供应商：
艾美捷科技
- 宿主：
Mouse
- 应用范围：
ELISA,In vivo Neutralization
- 抗体英文名：
Human LGR5/GPR49, InVivo Block/Neutralizing Antibody
- 抗体名：
Human LGR5/GPR49, InVivo Block/Neutralizing Antibody
Human LGR5/GPR49, InVivo Block/Neutralizing Antibody，Human LGR5/GPR49, InVivo Block/Neutralizing Antibody，Human LGR5/GPR49, InVivo Block/Neutralizing Antibody,Human LGR5/GPR49, InVivo Block/Neutralizing Antibody
产品名称：Human LGR5/GPR49, InVivo Block/Neutralizing Antibody-Human LGR5/GPR49, InVivo Block/Neutralizing Antibody
产品货号：BGT-ANT-37380
产品规格：100ug#1mg
应用类型：ELISA,In vivo Neutralization
蛋白别名：Leucine-rich repeat-containing G-protein coupled receptor 5, G-protein coupled receptor 49, G-protein coupled receptor 67, G-protein coupled receptor HG38, LGR5, GPR49, GPR67
Human LGR5/GPR49, InVivo Block/Neutralizing Antibody-Human LGR5/GPR49, InVivo Block/Neutralizing Antibody详情见产品datasheet
点击：Human LGR5/GPR49, InVivo Block/Neutralizing Antibody-Human LGR5/GPR49, InVivo Block/Neutralizing Antibody更多Biogradetech产品信息价格，货期，产品说明，百度搜“艾美捷科技”进入官网网站，查看具体产品且快速下单。
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文献和实验Human FastTrack mRNA Isolation
. 8.Incubate for 2 minutes at room temperature. Vortex the sample to resuspend the cellulose completely. 9.Rock the tube gently in a horizontal position for 60-90 minutes at room temperature. 10.Centrifuge the oligo(dT) slurry at 3,000 x g for 5 minutes
1 to a tube. 2) Add 20 μl of Antibody Mix. 3) Mix well and incubate for 20 min at 2–8°C. 4) Wash the cells by adding 2 ml Buffer 1. Mix well by tilting the tube several times and centrifuge at 300 x g for 10 min at 2–
(1 ). In our laboratory, we have developed methods to immortalize specific antibody-producing cells by fusing secreting EBV-activated lymphocytes to mouse-human heteromyeloma cell lines with electrofusion, followed by cloning (2 ). This methodology has allowed
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