PBS (pH 7.3) containing 1% stabilizing protein, 50% glycerol and 0.02% sodium azide.This antibody is supplied in a stabilized formulation. Compatibility with conjugation reactions depends on the chemistry of the conjugation method used. For conjugation me
HEK293T cells transfected with either BSG (Myc-DDK-tagged) overexpress plasmid (Red) or empty vector control plasmid (Blue) were immunostained by anti-BSG antibody (M00248-2)
Anti-BSG mouse monoclonal antibody (M00248-2) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY BSG.
Immunofluorescent staining of HT29 cells using anti-BSG mouse monoclonal antibody (M00248-2).
Immunohistochemical staining of paraffin-embedded Human prostate tissue within the normal limits using anti-BSG mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
Immunohistochemical staining of paraffin-embedded Human Kidney tissue within the normal limits using anti-BSG mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer
HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY BSG (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-BSG.
Western blot analysis of extracts (10ug) from 10 Human tissue by using anti-BSG monoclonal antibody at 1:500 (1: Testis, 2: Omentum, 3: Uterus, 4: Breast, 5: Brain, 6: Liver, 7: Ovary, 8: Thyroid gland, 9: colon,10: spleen).
Western blot analysis of extracts (35ug) from 9 different cell lines by using anti-BSG monoclonal antibody.
Equivalent amounts of cell lysates (10 ug per lane) of wild-type 293T cells (WT) and BSG-Knockout 293T cells (KO) were separated by SDS-PAGE and immunoblotted with anti-BSG monoclonal antibody M00248-2 (1:2000 ). Then the blotted membrane was stripped and reprobed with anti-PCNA antibody as a loading control.
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