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Anti-SERPINA1 TRUEMAB Antibody clone 11G2
TrueMAB Antibodies - Made against Authentic Protein Antigens
Also for SERPINA1 (NM_000295)
|Protein expressed in 293T cell transfected with human SERPINA1 expression vector|
|Human , Dog , Monkey
|WB, IHC, IP
||WB 1:1000~2000, IHC 1:150, IP 2ug/500ul
|PBS (pH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.|
|Purified from mouse ascites fluids by affinity chromatography (Protein A or G Sepharose)
|Homo sapiens serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1 (SERPINA1), transcript variant 1|
|A1A; A1AT; AAT; alpha1AT; PI; PI1; PRO2275|
|The protein encoded by this gene is secreted and is a serine protease inhibitor whose targets include elastase,plasmin, thrombin, trypsin, chymotrypsin, and plasminogen activator. Defects in this gene can cause emphysema or liver disease. Several transcript variants encoding the same protein have been found for this gene.|
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HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SERPINA1 (RC202082, 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.
Western blot analysis of extracts (35ug) from 9 different cell lines by using anti-SERPINA1 monoclonal antibody.
Immunohistochemical staining of paraffin-embedded Human Kidney tissue using anti-SERPINA1 mouse monoclonal antibody. (TA500378)
Immunohistochemical staining of paraffin-embedded Human liver tissue using anti-SERPINA1 mouse monoclonal antibody. (TA500378)
Immunohistochemical staining of paraffin-embedded Human pancreas tissue using anti-SERPINA1 mouse monoclonal antibody. (TA500378)
Immunoprecipitation(IP) of SERPINA1 by using TrueMab monoclonal anti-SERPINA1 antibodies (Negative control: IP without adding anti-SERPINA1 antibody.). For each experiment, 500ul of DDK tagged SERPINA1 overexpression lysates (at 1:5 dilution with HEK293T lysate), 2ug of anti-SERPINA1 antibody and 20ul (0.1mg) of goat anti-mouse conjugated magnetic beads were mixed and incubated overnight. After extensive wash to remove any non-specific binding, the immuno-precipitated products were analyzed with rabbit anti-DDK polyclonal antibody.