نتایج جستجو برای: digoxigenin

تعداد نتایج: 744  

Journal: :BioTechniques 1993
N Walter C Steiner

A fast and simple assay for T7 RNA polymerase based upon chemiluminescent detection of the synthesized, digoxigenin-labeled RNA on a nylon membrane with anti-digoxigenin coupled alkaline phosphatase and CSPD as substrate is described. Activity of RNA polymerase is determined with high sensitivity by quantifying the emitted light of the microplate-formatted dot-blot membrane with a photon counti...

Journal: :Molecular vision 2004
Ivaylo Stoilov Tayebeh Rezaie Ingela Jansson John B Schenkman Mansoor Sarfarazi

PURPOSE To examine the embryonic expression of cytochrome P4501b1 (Cyp1b1) gene by whole mount in situ hybridization. METHODS FVB/NcrlBR mouse embryos staged at 9.5, 10.5, and 11.5 dpc were obtained by timed breeding experiments. Antisense and sense RNA probes labeled with digoxigenin UTP were generated by in vitro transcription of an 848 bp Cyp1b1 cDNA fragment that was subcloned into transc...

Journal: :Nucleic acids research 1997
A K Lockley C G Jones J S Bruce S J Franklin R G Bardsley

By extending functional primers attached to a solid phase and incorporating a digoxigenin label, it is possible to visualise PCR products as discrete spots on specific regions of a solid support after colorimetric detection. The technique has been used for the detection of the point mutation associated with porcine malignant hyperthermia.

Journal: :Electrophoresis 1998
P Scholler S Heber J D Hoheisel

Large-scale hybridization-based genome mapping projects, such as the production of sequence-ready physical clone maps, call for robust and cheap DNA labeling techniques that are amenable to automation. We routinely use a high-throughput protocol based on fluorescence detection. DNA probes are labeled via polymerase chain reaction (PCR) amplification with primers that are digoxigenin-modified at...

2013
C. Panke D. Weininger A. Haas F. Schelter T. Schlothauer S. Bader R. Sircar H.P. Josel U. Baer H. Burtscher O. Mundigl M. Grote U. Brinkmann C. Sustmann

Flow cytometry is an established method for fast and accurate quantitation of cellular protein levels and requires fluorescently labeled antibodies as well as calibration standards. A critical step for quantitation remains the production of suitable detection antibodies with a precisely defined ratio of antigen-binding sites to fluorophores. Problems often arise as a consequence of inefficient ...

Journal: :Molecular biotechnology 1994
E Davies R Hodge P G Isaac

This article describes nonradioactive probing of a Northern blot. The method employs digoxigenin-labeled probes. Antidigoxigenin antibody/alkaline phosphate conjugate, and a chemiluminescent substrate are subsequently used in the detection system.

2015
Yasuhiko Higashi Yukari Ikeda Norihiko Yamamoto Youichi Fujii

We previously developed a radioimmunoassay for digoxin using an antiserum raised against digoxin 3’-hemisuccinate -bovine serum albumin. In the present study, we aimed to establish an enzyme immunoassay (EIA) for measuring serum digoxin level in patients, using digoxin 3’-hemisuccinate-β-D-galactosidase as an enzyme-labeled antigen. The developed enzyme immunoassay showed a quantification range...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید