- ￥3000 - 3999
- Abbiotec
- 美国
- 250593
- 2025年07月16日
- E, WB, IHC
- Rabbit
- M, R
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
KLH-conjugated synthetic peptide encompassing a sequence within the center region of mouse ICAM-1.
- 亚型：
Rabbit Ig
- 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-G affinity chromatography.
- 保存条件：
Store at -20°C.
- 克隆性：
多克隆抗体
- 标记物：
见下方详细说明
- 适应物种：
M, R
- 宿主：
Rabbit
- 应用范围：
E, WB, IHC
- 浓度：
见详细说明信息
- 靶点：
CD54
- 抗体英文名：
CD54 Antibody
- 抗体名：
CD54 Antibody
- 规格：
0.1 mg
CD54 Antibody产品详细介绍：
| 产品名称： | CD54 Antibody |
| 说明书： | http://www.abbiotec.com/antibodies/cd54-antibody【参考图片】 |
| 货号： | 250593 |
| 规格： | 0.1 mg |
| 产品描述： | ICAM-1 (Intracellular adhesion molecule 1) is the ligand for the leukocyte adhesion protein LFA-1 (integrin alpha-L/beta-2). During leukocyte trans-endothelial migration, ICAM-1 promotes the assembly of endothelial apical cups through SGEF and RHOG activation. ICAM-1 is a cellular receptor for rhinoviruses. |
| 克隆类型： | Rabbit Polyclonal Antibody |
| 亚型： | Rabbit Ig |
| 免疫原： | KLH-conjugated synthetic peptide encompassing a sequence within the center region of mouse ICAM-1. |
| 适用物种： | M, R |
| 应用范围： | E, WB, IHC |
| 应用说明： | E: 1:500-1:1,000; WB: 1:200-1:500; IHC: 1:200-1:500 |
| 别名： | Intercellular adhesion molecule 1; ICAM-1; Major group rhinovirus receptor; CD54 antigen; ICAM1 |
| 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-G 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： | Schmutzhard J et al. 2011. Tropical Medicine & International Health. 16(8):914-922. PMID: 21554502. |
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文献和实验CD54 分子 CD54 常用单克隆抗体或代号： WEHI- CAMI,OKT27;(ICAM- 1) 主要表达细胞： 广泛 [AS] 分子质量(kDa)和结构： gp90- 115(IgSF) 功 能： 与LFA- 1、Mac- 1和CD43结合,细胞间粘附,鼻病毒受体,En上恶性疟原虫受体 CD54 Aka ICAM-1 (intercellular adhesion
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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