- ￥1608 - 2664
- abinScience
- France
- HP654247
- 2026年06月01日
- ELISA, FCM
- Mouse
- Human
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- 详细信息
- 文献和实验
- 技术资料
- 形态：
Liquid
- 保存条件：
4°C
- 克隆性：
单克隆
- 标记物：
PerCP
- 适应物种：
Human
- 保质期：
12 months
- 级别：
一抗
- 供应商：
武汉研升生物科技有限公司
- 宿主：
Mouse
- 应用范围：
ELISA, FCM
- 抗体英文名：
Anti-Human HHLA2 Antibody (18C3), PerCP
- 规格：
50T/100T
| 规格： | 50T | 产品价格： | ￥1608.0 |
|---|---|---|---|
| 规格： | 100T | 产品价格： | ￥2664.0 |
| Product name | Anti-Human HHLA2 Antibody (18C3), PerCP |
| Catalog No. | HP654247 |
| Target | HHLA2, HERV-H LTR-associating protein 2, Human endogenous retrovirus-H long terminal repeat-associating protein 2 |
| Clone ID | 18C3 |
| Accession | Q9UM44 |
| Clonality | Monoclonal |
| Isotype | IgG2a |
| Host species | Mouse |
| Species reactivity | Human |
| Applications | ELISA, FCM |
| Conjugation | PerCP |
| Form | Liquid |
| Storage buffer | 0.01M PBS, pH 7.4, 0.2% BSA, 0.05% Proclin 300. |
| Stability and Storage | Store at 4°C for 12 months. Protect from light. Do not freeze. |
| Note | For flow cytometric staining, the suggested use of this reagent is 0.5 µg per million cells in 100 µL volume. It is recommended that the reagent be titrated for optimal performance for each application. For research use only. |
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文献和实验Simultaneous Quantification of t(14;18) and HPRT Exon 2/3 Deletions in Human Lymphocytes
is required for the formation of functional T-cell receptor genes in T cells and antibody genes in B cells. This is an inherently dangerous process, however, because double-strand breaks are introduced into the chromosomes. Molecular evidence indicates
[欢迎下载]：Antibody Engineering： Methods and Protocols
. coli 15 Expression of Recombinant Antibodies in Mammalian Cell Lines 16 Human Antibody Production Using Insect-Cell Expression Systems 17 Antibody Production in Transgenic Plants 18 Directed Mutagenesis of Antibody Variable Domains 19 Antibody
(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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