- 询价
- SA202
- 2025年07月15日
- ELISA;Western Blotting
- 0
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- 详细信息
- 文献和实验
- 技术资料
- 应用范围：
ELISA;Western Blotting
- 宿主：
0
- 库存：
大量
- 抗原来源：
0
- 是否单克隆：
0
- 规格：
1 mL
- ELISA
- Western Blotting
- Immunohistochemistry
The final working dilution is dependent on the specific assay conditions. However, good results can be expected with dilutions in the following ranges:
ELISA: 1/500 - 1/10,000
Immunohistochemistry: 1/40 - 1/1,000
NOTE: Do not dilute into buffers containing sodium azide, as this inhibits peroxidase.
- ELISA Reagents
- Immunohistochemistry Reagents
更多产品技术资讯，请访问密理博中国博客：http://blog.milliporechina.com
详细描述见链接：http://www.millipore.com/catalogue/item/SA202
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文献和实验Western Blotting with Horseradish Peroxidase Conjugates
7.5, 100mM NaCl, 0.1% Tween 20). Incubate the blot for 30 minutes at 37°C, 1 hour at room temperature, or overnight at 4°C. INCUBATION WITH HORSERADISH PEROXIDASE CONJUGATED ANTIBODY NOTE: THE INCLUSION OF SODIUM AZIDE IS TO BE AVOIDED
In Vitro PhagosomeEndosome Fusion
loaded endosomes and magnetic streptavidin conjugated bead-containing phagosomes. Fusion is quantified using a fluorescence-based detection method that measures the peroxidase activity associated with the beads.
Detection of apoptotic process in situ using immunocytochemical and TUNEL assays
antibody (mAb) conjugated with peroxidase (anti-DNA-POD) was used. This anti-DNA-POD mAb binds to single- and double-stranded, low molecular weight DNA fragments (mono- and oligonucleosomes), showing the internucleosomal degradation of genomic DNA occuring
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