- ￥3000 - 3999
- Abbiotec
- 美国
- 250580
- 2026年05月02日
- E, WB, IHC
- Rabbit
- H, 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 N-term region of human CCR-2.
- 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：
H, M, R
- 宿主：
Rabbit
- 应用范围：
E, WB, IHC
- 浓度：
见详细说明信息
- 靶点：
CCR-2
- 抗体英文名：
CCR-2 Antibody
- 抗体名：
CCR-2 Antibody
- 规格：
0.1 mg
CCR-2 Antibody产品详细介绍：
| 产品名称： | CCR-2 Antibody |
| 说明书： | http://www.abbiotec.com/antibodies/ccr-2-antibody【参考图片】 |
| 货号： | 250580 |
| 规格： | 0.1 mg |
| 产品描述： | CCR2 is the receptor for the MCP-1, MCP-3 and MCP-4 chemokines. CCR2 transduces a signal by increasing the intracellular calcium ion level. CCR2 is also the coreceptor with CD4 for HIV-1 infection. Variations in CCR2 are associated with relative resistance to immunodeficiency virus type 1. |
| 克隆类型： | Rabbit Polyclonal Antibody |
| 亚型： | Rabbit Ig |
| 免疫原： | KLH-conjugated synthetic peptide encompassing a sequence within the N-term region of human CCR-2. |
| 适用物种： | H, 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： | C-C chemokine receptor type 2; C-C CKR-2; CC-CKR-2; CCR-2; CCR2; Monocyte chemoattractant protein 1 receptor; MCP-1-R; CD192 antigen; CMKBR2 |
| 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： |
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文献和实验); CSB-MP004843HU Recombinant Human C-C chemokine receptor type 4 (CCR4) (Active); CSB-CF004843HU ● CCR4 抗体 CCR4 Recombinant Monoclonal Antibody; CSB-RA004843MA01HU CCR4 Antibody; CSB-PA004843LA01HU 参考文献： [1] Kayoko Hase, K. Tani, Teruki
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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