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文献和实验Detecting Low‐Affinity Extracellular Protein Interactions Using Protein Microarrays
Aluminum foil Plate reader (e.g., PHERAStar Plus; BMG Labtec) 30,000‐MWCO (molecular weight cut
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
-thalassemia point mutations in Iranians using a PCR-ELISA genotyping system. 文章Molecular Detection of Galactosemia Mutations by PCR-ELISA 有step by step的protocol。 Fig 2 - Molecular Detection of Galactosemia Mutations by PCR-ELISA PCR-ELISA
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