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- 详细信息
- 文献和实验
- 技术资料
- 库存:
1000
- 供应商:
上海钰博
- 检测范围:
见说明书
- 检测方法:
酶联免疫
- 应用:
科研
- 标记物:
见说明书
- 样本:
血清/组织/尿液
白血病抑制因子(LIF)检测试剂盒
检测范围 31.25-2000pg/mL 灵敏度 12.7pg/mL
样本类型 Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
实验时长 4.5h 实验方法 双抗夹心法
规格 96T
白血病抑制因子(LIF)检测试剂盒
| Organism species | Homo sapiens (Human) |
| Product No. | SEA085Hu |
| Sample type | Serum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids. |
| Format | 96T |
| Assay length | 4.5 hours |
| Detection range | 31.25-2000pg/mL The standard curve concentrations used for the ELISA’s were 2000pg/mL, 1000pg/mL, 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL, 31.25pg/mL |
| Sensitivity | The minimum detectable dose of this kit is typically less than 12.7pg/mL. |
No significant cross-reactivity or interference between Leukemia Inhibitory Factor (LIF) and analogues was observed.
| Matrix | Recovery range (%) | Average(%) |
| serum(n=5) | 80-89 | 85 |
| EDTA plasma(n=5) | 83-104 | 94 |
| heparin plasma(n=5) | 90-102 | 99 |
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Leukemia Inhibitory Factor (LIF) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%
| Sample | 1:2 | 1:4 | 1:8 | 1:16 |
| serum(n=5) | 89-103% | 89-96% | 83-91% | 95-105% |
| EDTA plasma(n=5) | 99-105% | 80-103% | 98-105% | 98-105% |
| heparin plasma(n=5) | 81-96% | 85-102% | 90-102% | 78-102% |
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
| Reagents | Quantity | Reagents | Quantity |
| Pre-coated, ready to use 96-well strip plate | 1 | Plate sealer for 96 wells | 4 |
| Standard | 2 | Standard Diluent | 1×20mL |
| Detection Reagent A | 1×120µL | Assay Diluent A | 1×12mL |
| Detection Reagent B | 1×120µL | Assay Diluent B | 1×12mL |
| TMB Substrate | 1×9mL | Stop Solution | 1×6mL |
| Wash Buffer (30 × concentrate) | 1×20mL | Instruction manual | 1 |
2. Add 100µL standard or sample to each well. Incubate 2 hours at 37oC;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37oC;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37oC;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 15-25 minutes at 37oC;
8. Add 50µL Stop Solution. Read at 450nm immediately.
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文献和实验上海西唐生物科技有限公司 021-55229872, 65333639 www.westang.com 人白血病抑制因子 (LIF)ELISA 试剂盒 ( 用于血清、血浆、细胞培养上清液和其它生物体液内 ) 原理 本实验采用双抗体夹心 ABC-ELISA 法。用抗人 LIF 单抗包被于酶标板上,标准品和样品中的 LIF与单抗结合,加入生物素化的抗人 LIF ,形成
无白血病抑制因子条件下利用SC1(pluripotin)维持小鼠胚胎干细胞的自我更新
小鼠胚胎干细胞常规培养时需要用到白血病抑制因子(LIF),但是LIF非常昂贵。本视频将展示一种很实惠的替代方法,即以小分子SC1代替LIF维持小鼠胚胎干细胞自我更新。 0:00 无白血病抑制因子条件下利用SC1(pluripotin)维持小鼠胚胎干细胞的自我更新 0:08 内容简介 0:51 维持小鼠胚胎干细胞的自我更新 3:11 免疫细胞化学法检测多潜能标记 4:54 SC1存在条件下小鼠干细胞生长的代表性图像结果 5:28 结论 无白血病抑制因子条件下利用SC
Joy Aho1, Michael O’Connor2, Elizabeth Hughes3, Thom Saunders3, Electra Coucouvanis1, and Jessie Ni1 摘要 在转基因和敲除研究中,维持多能性对利用小鼠胚胎干(ES)细胞至关重要。已经发现许多因子可以影响ES细胞的多能性,其中之一就表现在白血病抑制因子(LIF)对ES细胞培养的影响。关于抑瘤素M(OSM)能补偿LIF在ES细胞培养中的作用,对此存在不一致的报道。一些研究提示
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