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- 详细信息
- 文献和实验
- 技术资料
- 供应商:
安诺伦(北京)生物科技有限公司
- 检测范围:
0.156-10 ng/ml
- 检测方法:
Spectrophotometrical
- 应用:
Competitive
- 适应物种:
General
- 样本:
This immunoassay kit allows for the in vitro quantitative determination in Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids.
- 规格:
96T
试剂盒组分:Assay Plate, Standard, Sample Diluent, Assay Diluent A&B, Detection Reagent A&B, Wash Buffer, Substrate, Stop Solution.
功能:It is normally involved in the metabolism of every cell of the human body, especially affecting DNA synthesis and regulation, but also fatty acid synthesis and energy production.
储存条件:Store at +4°C. Please refer to protocols.
产品概述:General VB12/Vitamin B12 ELISA Kit is a ready-to-use microwell, strip plate ELISA (enzyme-linked immunosorbent assay) Kit designed for the quantitative measurement of VB12 in biological samples. Our rigorously validated, ready-to-go General VB12/Vitamin B12 ELISA Kit use a simple protocol that easily integrates into your current processes, allowing you to rapidly and accurately detect VB12 in your samples. Appropriate sample types may include Cell Culture Supernates, Serum, Platelet-poor EDTA Plasma, Platelet-poor Heparin Plasma, Urine.
Precision
Intra-Assay Precision (Precision within an assay): Three samples of known concentration were tested several times on one plate to assess intra-assay precision.
Inter-Assay Precision (Precision between assays): Three samples of known concentration were tested in several separate assays to assess inter-assay precision. Assays were performed by at least two technicians using two lots of components.
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文献和实验Guide to Cell Proliferation and Apoptosis Methods
1.3.2.1 Assays the measure plasma membrane leakage 51 Cytotoxicity Detection Kit (LDH) 52 Cellular DNA Fragmentation ELISA 54
实际上将作为阴性对照使用。CST 推荐使用 Histone H3 (D2B12) XP® Rabbit mAb (ChIP Formulated) #4620。该抗体可检测与基因组中所有 DNA 序列结合的所有组蛋白 H3 类型(H3、H3.3、CENP-A)。因此,不管检测的位点活性状态如何,该抗体都能为 ChIP 实验提供通用的阳性对照。 阴性对照 阴性对照抗体(如正常兔 IgG)不能识别特异抗原表位,因此可用于检测非特异性结合。例如,如果阴性对照样品中的产物量等于特异
importance of transcription factors in mediating gene regulation, there exists no general, genome-wide tool that uses transcription factors to induce or silence a target gene or select for a particular phenotype. In the strategy described here, we prepared
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