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In situ hybridization with non-radioactive digoxigenin-11-UTP-labeled cRNA probes: Localization of developmentally regulated mouse tenascin mRNAs
T. Tsukamoto
, M. Kusakabe, Y. Saga
Research output
:
Contribution to journal
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Article
›
peer-review
49
Citations (Scopus)
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Dive into the research topics of 'In situ hybridization with non-radioactive digoxigenin-11-UTP-labeled cRNA probes: Localization of developmentally regulated mouse tenascin mRNAs'. Together they form a unique fingerprint.
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Neuroscience
Staining Technique
100%
Uridine Triphosphate
100%
Digoxigenin
100%
In Situ Hybridization
100%
Antisense RNA
100%
Purkinje Cell
66%
Proteinase K
66%
Glial Cells
33%
Gene Expression
33%
Carcinogenesis
33%
Cerebellum
33%
Alkaline Phosphatase
33%
RNA Sequence
33%
Glycoprotein
33%
Extracellular Matrix
33%
Keyphrases
Probe Localization
100%
Digoxigenin
100%
Proteolytic Digestion
33%
Alveolar Wall
16%
Isotopic Labeling
16%
K Treatment
16%
Fixed Tissue
16%
Spatiotemporal Regulation
16%
Signal Detection
16%
Extracellular Matrix Glycoprotein
16%
Type I Pneumocyte
16%
Chromogenic Staining
16%
Poor Quality
16%
Biochemistry, Genetics and Molecular Biology
RNA Probe
100%
Signal Detection
16%
Type I Pneumocyte
16%
Glial Cells
16%
Immunology and Microbiology
Signal Detection
33%