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- 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:
APC
- 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:
FCM
- 抗体英文名:
Anti-Human GZMB Antibody (scFv17), APC
- 规格:
50T/100T
| 规格: | 50T | 产品价格: | ¥1740.0 |
|---|---|---|---|
| 规格: | 100T | 产品价格: | ¥2892.0 |
| Product name | Anti-Human GZMB Antibody (scFv17), APC |
| Catalog No. | HY574237 |
| Target | Cathepsin G-like 1, Granzyme-2, GZMB, grzmB, Fragmentin-2, Human lymphocyte protein, HLP, CTLA-1, CGL1, CTSGL1, CSPB, Lymphocyte protease, T-cell serine protease 1-3E, Granzyme B, CTLA1, GRB, Granzyme-B, C11, Cytotoxic T-lymphocyte proteinase 2, SECT |
| Clone ID | scFv17 |
| Accession | P10144 |
| Clonality | Monoclonal |
| Isotype | IgG1 |
| Host species | Mouse |
| Species reactivity | Human |
| Applications | FCM |
| Conjugation | APC |
| 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Phage Libraries for Generation of Anti-Botulinum scFv Antibodies
, including antibodies of human origin, which cannot be easily obtained by conventional hybridoma technology. Recent advances in the expression of antibody fragments in E. coli (2 ,3 ) and the application of the polymerase chain reaction (4 ) for cloning
Cloning Single-Chain Antibody Fragments (ScFv) from Hyrbidoma Cells
several limitations of using hybridoma-derived antibodies. The source of the hybridoma clones are mostly rat or mouse B-lymphocytes. Therefore a human-anti-mouse or human-anti-rat antibody response may result in immunogenicity of these antibodies. This leads
during library construction is of utmost importance for the quality. This chaper describes the generation of human naive or immune scFv antibody gene libraries by a two step cloning strategy. The method has already been proven for the generation of very high
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