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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20°C储存;避免反复冻融
- 供应商:
上海阿拉丁生化科技股份有限公司
- 浓度:
ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL
- 抗体英文名:
A35R Mouse mAb
设定黄金标准,在阿拉丁,我们不仅相信保持质量,而且相信质量。 我们的目标是定义它。 我们的质量管理理念为业界研究试剂建立了高质量的标准。 当您听到阿拉丁这个名字时,就会知道它是各个方面坚定不移品质的灯塔。
说明:产品表货号最后一段中横杠后的重量为产品的包装规格,例如A123456-500g,该货号对应的包装规格为500g。
中文名:A35R Mouse mAb
英文名:A35R Mouse mAb
中文别名:-
英文别名:-
纯度:ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL
cas号:-
产品介绍:-
| 货号(SKU): | 纯度: | 价格: | 库存: |
| Ab186123-1ml | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 16999.9 | 0 |
| Ab156140-1ml | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 16999.9 | 0 |
| Ab186123-100μl | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 2099.9 | 1 |
| Ab156140-100μl | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 2099.9 | 4 |
| Ab186123-50μl | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 1299.9 | 4 |
| Ab156140-50μl | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 1299.9 | 5 |
| Ab186123-10μl | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 499.9 | 10 |
| Ab156140-10μl | ExactAb™, Validated, Carrier Free, Azide Free, ≥95%(SDS-PAGE&SEC), 1.0 mg/mL | 499.9 | 10 |
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文献和实验(adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10
Purification of mAb (IgG) by Chang-Duk Jun, 03/14/2000 Purpose Materials Antibody 7E3 , 2L sup grown in flasks, frozen and thawed overnight. BioRad Affi-Gel Protein A MAPS II Buffers
T-Cell Activation Using mAb to CD3
One of the most common ways to assess T cell activation is to measure T cell proliferation upon in vitro stimulation of T cells via antigen or agonistic antibodies to TCR. This protocol is written as a starting point for examining in vitro proliferation of mouse
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