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- 文献和实验
- 技术资料
- 库存:
100
- 供应商:
上海博湖
- 检测范围:
0.312-20ng/ml
- 检测方法:
Sandwich ELISA, Double Antibody
- 应用:
0.188ng/ml
- 样本:
LRP11
- 规格:
96T
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文献和实验in the same volume of Buffer 1 as the initial volume transferred from the vial in step 2. 2. Sample Preparation Preparation of MNC from Buffy Coat to Obtain Low Platelet Numbers 1) Dilute 10 – 18 ml buffy coat with Buffer 2 to a total
Quantification of Human IgG and Related Fc Fusion Proteins by a Human IgG/Fc Capture ELISA
of recombinant human IgGs after production and purification for further assays. Here, we describe a human IgG/Fc capture enzyme linked immunosorbent assay (ELISA) which is simple, robust, inexpensive and specific for all types of human IgGs and related Fc fusion
Detecting Low‐Affinity Extracellular Protein Interactions Using Protein Microarrays
the throughput of assays capable of detecting transient extracellular protein interactions. These methodological improvements now permit screening for novel extracellular receptor?ligand interactions on a genome?wide scale. Curr. Protoc. Protein Sci. 72:27.5.1?27
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