Application
IP analysis was performed with 500ul of DDK tagged SERPINA1 overexpression lysates and either no antibody control, 2ug of or 2ug of The precipitated protein was detected by DDK tag antibody.
Application
HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SERPINA1 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-SERPINA1.
Application
Western blot analysis of extracts (35ug) from 9 different cell lines by using anti-SERPINA1 monoclonal antibody.
Application
Western blot analysis of 35ug of cell extracts from human brain tissue lysates using anti-SERPINA1 antibody.
Application
Immunohistochemical staining of paraffin-embedded Carcinoma of liver tissue using anti-SERPINA1mouse monoclonal antibody. ( Dilution 1:50)
Application
Immunohistochemical staining of paraffin-embedded pancreas tissue using anti-SERPINA1mouse monoclonal antibody. ( Dilution 1:50)
Application
Immunohistochemical staining of paraffin-embedded liver tissue using anti-SERPINA1mouse monoclonal antibody. ( Dilution 1:50)
Application
Immunohistochemical staining of paraffin-embedded Carcinoma of thyroid tissue using anti-SERPINA1mouse monoclonal antibody. ( Dilution 1:50)
Application
Immunohistochemical staining of paraffin-embedded Adenocarcinoma of endometrium tissue using anti-SERPINA1mouse monoclonal antibody. ( Dilution 1:50)
Application
Immunohistochemical staining of paraffin-embedded carcinoma of human liver tissue using anti-SERPINA1 mouse monoclonal antibody.
Application
Immunohistochemical staining of paraffin-embedded carcinoma of human thyroid tissue using anti-SERPINA1 mouse monoclonal antibody.
Application
Immunohistochemical staining of paraffin-embedded human pancreas tissue using anti-SERPINA1 mouse monoclonal antibody.
Application
HEK293T cells transfected with either SERPINA1 overexpress plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-SERPINA1 antibody , and then analyzed by flow cytometry.