BioTechniques ◽  
2000 ◽  
Vol 29 (5) ◽  
pp. 1012-1017 ◽  
Author(s):  
G. Patrone ◽  
F. Puppo ◽  
R. Cusano ◽  
M. Scaranari ◽  
I. Ceccherini ◽  
...  
Keyword(s):  
Rt Pcr ◽  

2018 ◽  
Vol 557 ◽  
pp. 46-58
Author(s):  
Aiichiro Muraoka ◽  
Yoshinori Matsuura ◽  
Hisashi Naitow ◽  
Makoto Ihara ◽  
Naoki Kunishima

2011 ◽  
Vol 74 (10) ◽  
pp. 1985-1993 ◽  
Author(s):  
Kohji Nagano ◽  
Takashi Shinkawa ◽  
Kuniyasu Kato ◽  
Noriyuki Inomata ◽  
Nami Yabuki ◽  
...  

2008 ◽  
Vol 3 (12) ◽  
pp. 1848-1861 ◽  
Author(s):  
Faqing Huang ◽  
Jun He ◽  
Yilin Zhang ◽  
Yanlin Guo

2016 ◽  
Vol 27 (8) ◽  
pp. 1188-1196 ◽  
Author(s):  
Dae In Kim ◽  
Samuel C. Jensen ◽  
Kyle A. Noble ◽  
Birendra KC ◽  
Kenneth H. Roux ◽  
...  

The BioID method uses a promiscuous biotin ligase to detect protein–protein associations as well as proximate proteins in living cells. Here we report improvements to the BioID method centered on BioID2, a substantially smaller promiscuous biotin ligase. BioID2 enables more-selective targeting of fusion proteins, requires less biotin supplementation, and exhibits enhanced labeling of proximate proteins. Thus BioID2 improves the efficiency of screening for protein–protein associations. We also demonstrate that the biotinylation range of BioID2 can be considerably modulated using flexible linkers, thus enabling application-specific adjustment of the biotin-labeling radius.


1989 ◽  
Vol 35 (4) ◽  
pp. 573-576 ◽  
Author(s):  
J Peters ◽  
H Schmidt-Gayk ◽  
B Peters ◽  
F P Armbruster ◽  
A Quentmeier ◽  
...  

Abstract In evaluating an enzyme-linked immunoassay of carcinoembryonic antigen (CEA) we found that the IgG fraction of polyclonal anti-CEA antibodies (DAKO) bound very well to the walls of polypropylene test tubes. We therefore developed an immunoradiometric CEA assay based on this binding of polyclonal anti-CEA antibody. We biotinylated a commercially available monoclonal antibody (Hybritech) and bound this to the CEA-anti-CEA bound to the tube wall. For detection we used 125I-labeled streptavidin. In comparison with several immunoassays for CEA this system offered several advantages such as greater linearity of the standard curve (from 0 to 74 micrograms/L), a steeper dose-response curve, and smaller coefficients of variation in the clinically useful range. This assay system may be used for other large molecules, so that only one tracer, the 125I-labeled streptavidin, has to be labeled; thus the technique seems suited for several different assays.


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