- ￥3000 - 3999
- Abbiotec
- 美国
- 250124
- 2025年07月14日
- FC, B
- Mouse
- H
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Soluble human CD89 protein
- 亚型：
mouse IgG1
- 形态：
Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-A affinity chromatography.
- 保存条件：
Store at -20°C.
- 克隆性：
单克隆抗体
- 标记物：
见下方详细说明
- 适应物种：
H
- 宿主：
Mouse
- 应用范围：
FC, B
- 浓度：
见详细说明信息
- 靶点：
CD89
- 抗体英文名：
CD89 Antibody
- 抗体名：
CD89抗体
- 规格：
0.1 mg
CD89 Antibody产品详细介绍：
| 产品名称： | CD89 Antibody |
| 说明书： | http://www.abbiotec.com/antibodies/cd89-antibody【参考图片】 |
| 货号： | 250124 |
| 规格： | 0.1 mg |
| 产品描述： | The CD89 antigen (Fc alpha receptor I) binds to the Fc region of immunoglobulins alpha (IgA). CD89 mediates several immune functions including cytokine production. CD89 consists of a membrane-distal Ig-like extracellular domain (EC1), a membrane-proximal Ig-like extracellular domain (EC2), a transmembrane region, and a short cytoplasmic tail. This antibody recognizes the EC1 domain of human CD89 by flow cytometry and also inhibits CD89 functions. |
| 克隆类型： | Mouse Monoclonal Antibody |
| 亚型： | mouse IgG1 |
| 免疫原： | Soluble human CD89 protein |
| 适用物种： | H |
| 应用范围： | FC, B |
| 应用说明： | B: 4 mg/4 x 105 cells; FC: 1 mg/0.1 ml. This antibody recognizes the EC1 domain of Fc alpha-RI extracellular region. |
| 别名： | Immunoglobulin alpha Fc receptor; IgA Fc receptor; CD89 antigen; FCAR; CD89 |
| 形态： | Each vial contains 0.1 mg IgG in 0.1 ml (1 mg/ml) of PBS pH7.4 with 0.09% sodium azide. Antibody was purified by Protein-A affinity chromatography. |
| 保存条件： | Store at -20°C. Minimize freeze-thaw cycles. Product is guaranteed one year from the date of shipment. |
| 参考文献： | Zhang, W et al. 2000. Clin. Exp. Immunol. 121: 106-111. PMID # 10886246. |
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文献和实验CD89 分子 CD89 常用单克隆抗体或代号： 79E6,A3;(Fca R) 主要表达细胞： My,Tsub,Bsub [M] 分子质量(kDa)和结构： gp55- 75(IgSF) 功 能： IgAFc段受体,信号转导 CD89 Summary: IgA Fc receptor, binds IgA and eliminates IgA coated targets
Generation of Antibody Molecules Through Antibody Engineering
been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional
The importance of antibody molecules was first recognized in the 1890s, when it was shown that immunity to tetanus and diphtheria was caused by antibodies against the bacterial exotoxins (1 ). Around the same time, it was shown that antisera
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