Quantization of bovine serum albumin by fluorescence enhancement effects and corresponding binding of macrocyclic host-protein assembly

2012 ◽  
Vol 106 ◽  
pp. 113-119 ◽  
Author(s):  
Munmun Bardhan ◽  
Tapas Misra ◽  
Tapan Ganguly
Keyword(s):  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Fluorescence Enhancement ◽  
Protein Assembly ◽  
Host Protein

scholarly journals Evaluation of Bovine Serum Albumin as a Fluorescence Enhancement Reagent in Liquid Chromatography.

1995 ◽  
Vol 11 (5) ◽  
pp. 743-747 ◽  
Author(s):  
Junichi ISHIDA ◽  
Kazutomo ABE ◽  
Masaru NAKAMURA ◽  
Masatoshi YAMAGUCHI
Keyword(s):  
Liquid Chromatography ◽  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Fluorescence Enhancement

scholarly journals Schiff base complex conjugates of bovine serum albumin as artificial metalloenzymes for eco-friendly enantioselective sulfoxidation

RSC Advances ◽  
2018 ◽  
Vol 8 (71) ◽  
pp. 40720-40730 ◽  
Author(s):  
Jie Tang ◽  
Pengfei Yao ◽  
Lina Wang ◽  
Hedong Bian ◽  
Meiyi Luo ◽  
...  
Keyword(s):  
Schiff Base ◽  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Schiff Base Complex ◽  
Docking Studies ◽  
Host Protein ◽  
Schiff Base Complexes ◽  
Uv Visible ◽  
Artificial Metalloenzymes

Artificial metalloenzymes have been prepared by non-covalent insertion of transition metal Schiff-base complexes into bovine serum albumin as the host protein and were characterized by UV-visible spectroscopy, ESI-TOF mass spectrometry and molecular docking studies.

Improvement of an artificial test substrate technique for evaluation of em immunocytochemical labeling

1987 ◽  
Vol 45 ◽  
pp. 762-763
Author(s):  
G. D. Gagne ◽  
M. F. Miller
Keyword(s):  
Bovine Serum Albumin ◽  
Serum Albumin ◽  
Bovine Serum ◽  
Artificial Substrate ◽  
Chemical Fixation ◽  
As If

We recently described an artificial substrate system which could be used to optimize labeling parameters in EM immunocytochemistry (ICC). The system utilizes blocks of glutaraldehyde polymerized bovine serum albumin (BSA) into which an antigen is incorporated by a soaking procedure. The resulting antigen impregnated blocks can then be fixed and embedded as if they are pieces of tissue and the effects of fixation, embedding and other parameters on the ability of incorporated antigen to be immunocyto-chemically labeled can then be assessed. In developing this system further, we discovered that the BSA substrate can also be dried and then sectioned for immunolabeling with or without prior chemical fixation and without exposing the antigen to embedding reagents. The effects of fixation and embedding protocols can thus be evaluated separately.

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