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- 详细信息
- 文献和实验
- 技术资料
- 英文名:
human CD3 MicroBeads
- 保质期:
1年
- 保存条件:
2-8°C
- 库存:
100⁺盒
- 供应商:
上海睿安生物13611631389
- 规格:
1✕10⁹ total cells/盒
美天旎Miltenyi货号130-050-101人CD3磁珠(human CD3 MicroBeads)上海睿安生物13611631389
该试剂盒用于从人外周血、支气管灌洗液、细胞培养物或者各种组织中正选CD3 T细胞。分离的T细胞可用于T细胞毒性、T细胞活化、HIV感染、信号转导和表面标记表达等研究。 |
优点: |
- 操作简单;- 分离快速。 |
数据: |
|
图1. 使用CD3微磁珠和带有MS分选柱的MiniMACS™分离器从PBMC中分离CD3 +细胞。 |
组成成分: |
▪ 人CD3磁珠:与抗人CD3单克隆抗体(同型:小鼠IgG2a)偶联的磁珠,2ml |
相关产品: |
▪ MS分选柱(美天旎Miltenyi货号130-042-201)▪ LS分选柱(美天旎Miltenyi货号130-042-401)▪ 磁力架(美天旎Miltenyi货号130-042-303)▪ MS分选磁极(美天旎Miltenyi货号130-042-102)▪ Rinsing solution(美天旎Miltenyi货号130-091-222)▪ Running buffer(美天旎Miltenyi货号130-091-221) |
Specifications for CD3 MicroBeads, human
Overview
CD3 MicroBeads were developed for positive selection or depletion of CD3+ T cells from peripheral blood, bronchial lavage, cell culture, or various tissues such as lymphoid, nasal, and tumor tissue.
Detailed product information
Background information
CD3 is expressed on all T cells and CD56+ NKT cells, and is associated with the T cell receptor. 70–80% of human peripheral blood lymphocytes and 65–85% of thymocytes are CD3+. The epitope recognized by CD3 MicroBeads is located on the CD3ε chain.
Downstream applications
T cells isolated by MACS® Technology have been used for various studies, e.g., on T cell cytotoxicity, T cell activation1, HIV infectivity2, signal transduction, and surface marker expression.
Columns
For positive selection: MS, LS, XS, or autoMACS® Columns. For depletion: LD, D, or autoMACS Columns.

References for CD3 MicroBeads, human(部分文献)
Publications
Pitti, R. M. et al. (1998) Genomic amplification of a decoy receptor for Fas ligand in lung and colon cancer. Nature 396: 699-703
Nicoll, G. et al. (2003) Ganglioside GD3 expression on target cells can modulate NK cell cytotoxicity via siglec-7-dependent and -independent mechanisms. Eur. J. Immunol. 33: 1642-1648
Heath, S. L. et al. (1995) Follicular dendritic cells and human_immunodeficiency virus infectivity. Nature 377: 740-744
Lorenzen, D. R. et al. (1999) Immunoglobulin A1 protease, an exoenzyme of pathogenic Neisseriae, is a potent inducer of proinflammatory cytokines. J. Exp. Med. 190: 1049-1058
Klein, U. et al. (1994) Variable region gene analysis of B cell subsets derived from a 4-year-old child: somatically mutated memory B cells accumulate in the peripheral blood already at young age. J. Exp. Med. 180: 1383-1393
Heidenreich, F. and Jovin, T. (1996) Synthesis of anti-acetylcholine receptor antibodies by CD5- B cells from peripheral blood of myasthenia gravis patients. J. Neurol. 243: 57-62
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文献和实验美天旎Miltenyi货号130-050-101人CD3磁珠(human CD3 MicroBeads)上海睿安生物13611631389
该试剂盒用于从人外周血、支气管灌洗液、细胞培养物或者各种组织中正选CD3 T细胞。分离的T细胞可用于T细胞毒性、T细胞活化、HIV感染、信号转导和表面标记表达等研究。 |
优点: |
- 操作简单;- 分离快速。 |
数据: |
|
图1. 使用CD3微磁珠和带有MS分选柱的MiniMACS™分离器从PBMC中分离CD3 +细胞。 |
组成成分: |
▪ 人CD3磁珠:与抗人CD3单克隆抗体(同型:小鼠IgG2a)偶联的磁珠,2ml |
相关产品: |
▪ MS分选柱(美天旎Miltenyi货号130-042-201)▪ LS分选柱(美天旎Miltenyi货号130-042-401)▪ 磁力架(美天旎Miltenyi货号130-042-303)▪ MS分选磁极(美天旎Miltenyi货号130-042-102)▪ Rinsing solution(美天旎Miltenyi货号130-091-222)▪ Running buffer(美天旎Miltenyi货号130-091-221) |
Specifications for CD3 MicroBeads, human
Overview
CD3 MicroBeads were developed for positive selection or depletion of CD3+ T cells from peripheral blood, bronchial lavage, cell culture, or various tissues such as lymphoid, nasal, and tumor tissue.
Detailed product information
Background information
CD3 is expressed on all T cells and CD56+ NKT cells, and is associated with the T cell receptor. 70–80% of human peripheral blood lymphocytes and 65–85% of thymocytes are CD3+. The epitope recognized by CD3 MicroBeads is located on the CD3ε chain.
Downstream applications
T cells isolated by MACS® Technology have been used for various studies, e.g., on T cell cytotoxicity, T cell activation1, HIV infectivity2, signal transduction, and surface marker expression.
Columns
For positive selection: MS, LS, XS, or autoMACS® Columns. For depletion: LD, D, or autoMACS Columns.

References for CD3 MicroBeads, human(部分文献)
Publications
Pitti, R. M. et al. (1998) Genomic amplification of a decoy receptor for Fas ligand in lung and colon cancer. Nature 396: 699-703
Nicoll, G. et al. (2003) Ganglioside GD3 expression on target cells can modulate NK cell cytotoxicity via siglec-7-dependent and -independent mechanisms. Eur. J. Immunol. 33: 1642-1648
Heath, S. L. et al. (1995) Follicular dendritic cells and human_immunodeficiency virus infectivity. Nature 377: 740-744
Lorenzen, D. R. et al. (1999) Immunoglobulin A1 protease, an exoenzyme of pathogenic Neisseriae, is a potent inducer of proinflammatory cytokines. J. Exp. Med. 190: 1049-1058
Klein, U. et al. (1994) Variable region gene analysis of B cell subsets derived from a 4-year-old child: somatically mutated memory B cells accumulate in the peripheral blood already at young age. J. Exp. Med. 180: 1383-1393
Heidenreich, F. and Jovin, T. (1996) Synthesis of anti-acetylcholine receptor antibodies by CD5- B cells from peripheral blood of myasthenia gravis patients. J. Neurol. 243: 57-62







