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Titlebook: CCN Proteins; Methods and Protocol Masaharu Takigawa Book 2017 Springer Science+Business Media New York 2017 CCN proteins.Cyr61 (Cysteine-r

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978-1-4939-8197-7Springer Science+Business Media New York 2017
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Methods in Molecular Biologyhttp://image.papertrans.cn/c/image/220234.jpg
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https://doi.org/10.1007/978-3-663-07312-3sented. In this method, embryos are hybridized with Dig-labeled riboprobes, and the riboprobes are detected by use of the alkaline-phosphatase reaction in the presence of a 4-nitro-blue tetrazolium chloride and 5-bromo-4-chloro-3-indolyl-phosphate (NBT + BCIP) mixture. Obvious detection of positive
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https://doi.org/10.1007/3-540-28495-8erse transcriptase PCR (qPCR) quantifies mRNA levels of these key genes. Immunostaining localizes CCN proteins within skin tissue, and provides semiquantitative information regarding relative levels of the proteins. Reliable determinations of the expression levels of CCN genes and proteins are essen
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Zusammenfassung und Schlussfolgerungen,mounts of specific mRNA transcripts, done by measuring amplified levels of specific cDNAs. In this chapter, we provide our real-time RT-PCR experimental procedure using SYBR Green I for the quantitative analysis of CCN family gene expression. Especially, we describe the extraction and purification s
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Zusammenfassung und Schlussfolgerungen,s. These techniques give good results on cell culture but for organs that are made of numerous cells with several compartments, various states of differentiation as in epidermis, immunohistochemistry is always relevant. Double (triple) staining by immunofluorescence allows positive cells identificat
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