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- 详细信息
- 文献和实验
- 技术资料
- 供应商:
武汉益普生物科技有限公司
- 检测范围:
0.31-5 μg/mL
- 检测方法:
Colorimetric
- 样本:
Plasma, Serum
- 灵敏度:
0.156 μg/ml
- 规格:
96T
| 产品名 | Sirukumab ELISA Kit |
| 货号 | KDC15803 |
| 规格 | 96T |
| 别名 | CNTO 136, CAS: 1194585-53-9 |
| 检测方法 | Colorimetric |
| 样本类型 | Plasma, Serum |
| 实验类型 | Quantitative |
| 检测范围 | 0.31-5 μg/mL |
| 灵敏度 | 0.156 μg/ml |
| 回收率 | 80-120% |
| 精准度 | CV<20% |
| 背景 | Sirukumab (developmental code name CNTO-136) is a human monoclonal antibody (mAb) designed for the treatment of rheumatoid arthritis (RA). It acts against the proinflammatory cytokine interleukin (IL) -6 (IL-6). Sirukumab was evaluated in five Phase 3 studies of patients with RA. In September 2016, Janssen submitted a biologics license application (BLA) seeking approval of sirukumab for the treatment of moderately to severely active RA, but they announced in September 2017 that they received a complete response letter from the Food and Drug Administration (FDA) indicating additional clinical data were needed to further evaluate the safety of sirukumab in that patient population. Janssen subsequently decided not to pursue global approvals of sirukumab for the treatment of moderately to severely active RA. Sirukumab was being evaluated in a Phase 3 study (NCT02531633) of another inflammatory disease, giant cell arteritis. This study, sponsored by GlaxoSmithKline (GSK), was terminated in November 2017 due to GSK’s decision to return rights to sirukumab to Janssen and discontinue sirukumab development in giant cell arteritis. Also, in November 2017, a Phase 3 study (NCT02899026) sponsored by GSK of sirukumab in patients with polymyalgia rheumatica, an inflammatory disorder that causes muscle pain and stiffness, was withdrawn prior to enrollment. |
| 稳定性和存储 | The stability of ELISA kit is determined by the loss rate of activity. The loss rate of this kit is less than 10% prior to the expiration date under appropriate storage condition. |
| 保存方法 | 2-8 ℃ |
| 说明 | For Research Use Only. |

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文献和实验市面上的 ELISA 试剂盒五花八门,质量良莠不齐。如何浪里淘金,选择既符合科研需求,又品质上乘的 ELISA 试剂盒呢? 教你七招,快速搞定 ELISA 试剂盒的选择! 01 查找待测样本的蛋白浓度 通过检索 SCI 文献、Genecards、Mayocliniclabs 等,获得目标蛋白的表达部位及表达浓度参考值,比较 ELISA 试剂盒中给出的样本测值与参考值是否一致。 02 明确试剂盒的应用种属&检测的样本类型 不同厂家验证的样本类型不同。除试剂盒特别说明外,一般情况下,不同
本文主要介绍 ELISA 试剂盒、实验样本、相关问题,帮助大家更好地开展实验 试剂盒 Q1:科研试剂盒与临床试剂盒的区别 ? A1:临床试剂是经过权威机构认可的,如 FDA、CFDA 等;而科研试剂一般是厂家自主研制,不需要通过权威机构验证。 经营临床诊断类产品的机构需要取得《医疗器械经营企业许可证》;经营科研试剂的机构不需要此证件。 临床试剂盒一般仅用于检测人血清/血浆等较为单一的分泌性样本类型;科研试剂盒的样本检测种类、检测范围则比临床试剂盒宽广得多。但一般来说,临床试剂盒的质量
目前市场上的 ELISA 试剂盒质量参差不齐,如何去挑选适合自己的试剂盒就显得特别重要,具体有以下几点可供参考。 特异性 ELISA 试剂盒的特异性与试剂盒的关键组分,抗体对有关。若抗体对中之一为多抗,另一个必须为单抗,建议使用双单抗。 灵敏度 灵敏度反映的是试剂盒检出被检物质的最低量的能力,用户可根据自己样本中待检指标的量选择合适的试剂盒,如果待检指标量很低,一般的试剂盒不能满足要求,可选择高敏的 ELISA 试剂盒。 重复
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