Preparation and Preliminary Identification of Monoclonal Antibodies Against Human Endothelial Cell Specific Molecule-1
Yuan Wang
Abstract
Yuan Wang
Abstract
The human endothelial cell specific molecule-1 (ESM-1) was used as antigen to prepare monoclonal antibodies by means of the B lymphocyte hybridoma technique. Seven strains of hybridoma cells secreting anti human ESM-1 stably were obtained after PEG fusion and screening by limited dilution,in which the McAb3A7 secreted by one of the hybridoma cells showed the highest specificity with the agglutination titer of 1∶6 000. The subtype of the secreted antibody was IgG2b. This monoclonal antibody could recognize specifically the ESM-1 both in endothelial cells and supernatants of cell cultures. The distribution of ESM-1 was mainly in the cytoplasm of endothelial cells,and located in the vasculoendothelial cells of renal tissues. Higher expression of ESM-1 in renal cell carcinoma than that of normal renal tissues was also noticed. These results indicate that this monoclonal antibody shows both high sensitivity and specificity.
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
The human endothelial cell specific molecule-1 (ESM-1) was used as antigen to prepare monoclonal antibodies by means of the B lymphocyte hybridoma technique. Seven strains of hybridoma cells secreting anti human ESM-1 stably were obtained after PEG fusion and screening by limited dilution,in which the McAb3A7 secreted by one of the hybridoma cells showed the highest specificity with the agglutination titer of 1∶6 000. The subtype of the secreted antibody was IgG2b. This monoclonal antibody could recognize specifically the ESM-1 both in endothelial cells and supernatants of cell cultures. The distribution of ESM-1 was mainly in the cytoplasm of endothelial cells,and located in the vasculoendothelial cells of renal tissues. Higher expression of ESM-1 in renal cell carcinoma than that of normal renal tissues was also noticed. These results indicate that this monoclonal antibody shows both high sensitivity and specificity.
Key concepts: Monoclonal antibody, Molecular biology, Antibody, Cell fusion, Cell culture, Biology, Endothelial stem cell, Antigen