Visualization and quantitation of poly A+-mRNA by using in situ hybridization with biotinylated oligonucleotides.
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Visualization and quantitation of poly A+-mRNA by using in situ hybridization with biotinylated oligonucleotides. / Wehner, K; Fritz, P; Köhler, K; Multhaupt, H.
I: Acta histochemica. Supplementband, Bind 37, 1989, s. 83-8.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Visualization and quantitation of poly A+-mRNA by using in situ hybridization with biotinylated oligonucleotides.
AU - Wehner, K
AU - Fritz, P
AU - Köhler, K
AU - Multhaupt, H
N1 - Keywords: Hela Cells; Humans; Immunoenzyme Techniques; Neoplasm Proteins; Nucleic Acid Hybridization; Oligonucleotide Probes; Poly A; RNA, Messenger
PY - 1989
Y1 - 1989
N2 - HeLa cells and synovial tissue sections were used for visualizing poly A+-mRNA after in situ hybridization. We describe a method to biotinylate hybridization probes by tailing oligo-dT nucleotides with biotinyl-dUTP using terminal deoxynucleotidyl transferase (E.C.2.7.7.3.1.). The hybrids were detected by using the strepavidin-biotin-peroxidase complex (ABC method). The reaction product of the peroxidase staining in the cells and in the tissue sections, is quantitated by the method of plug- and scanning photometry respectively.
AB - HeLa cells and synovial tissue sections were used for visualizing poly A+-mRNA after in situ hybridization. We describe a method to biotinylate hybridization probes by tailing oligo-dT nucleotides with biotinyl-dUTP using terminal deoxynucleotidyl transferase (E.C.2.7.7.3.1.). The hybrids were detected by using the strepavidin-biotin-peroxidase complex (ABC method). The reaction product of the peroxidase staining in the cells and in the tissue sections, is quantitated by the method of plug- and scanning photometry respectively.
M3 - Journal article
C2 - 2505326
VL - 37
SP - 83
EP - 88
JO - Acta histochemica. Supplementband
JF - Acta histochemica. Supplementband
SN - 0567-7556
ER -
ID: 5240525