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- 抗体英文名:
p-NPP Substrate Buffer
- 规格:
500ML
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文献和实验DIRECT ELISA USING FLUORESCENT SUBSTRATE PROTOCOL
: TBS 250 μl/well; 3x 30 seconds.8. Amplify signal by adding 100 μl/well AttoPhos Fluorescent substrate system, for 5-10 min at RT. 36 mg ofAttoPhos substrate should be mixed with 60 ml of AttoPhos buffer 24 hours prior to use. Make sure well isclean
叮当儿 各位大侠,小妹要对HCE细胞的Toll样4受体做检测,但是细胞自身表达量太低,正常细胞提取RNA之后做逆转录都没有结果,而且我还要对其表达进行干扰,转染shRNA进去,结果就是做pcr时更没有结果了(内参很好),PCR反应条件如下: 20ul volum cDNA loading 3ul 10xtaq buffer 2ul dNTPs(2.5/each) 2ul Mg
Design and Preparation of Sequence-Specific RNase P Ribozymes
The catalytic RNA subunit of Escherichia coli RNase P (M1 RNA) is a structure-specific endonuclease that cleaves pre-tRNA substrates in trans . By combining catalytic and substrate RNAs in one RNA molecule, self-cleaving ribozymes
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