Western blot (WB): | 1:500-2000 |
Immunohistochemistry (IHC): | 1:50-400 |
Immunocytochemistry/Immunofluorescence (ICC/IF): | 1:50-400 |
Enzyme linked immunosorbent assay (ELISA): | 1:100-1000 |
(Boiling the paraffin sections in 10mM citrate buffer,pH6.0,or PH8.0 EDTA repair liquid for 20 mins is required for the staining of formalin/paraffin sections.) Optimal working dilutions must be determined by end user. |
Western blot analysis of HSD17B1 using anti-HSD17B1 antibody (A02198). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HSD17B1 antigen affinity purified polyclonal antibody (A02198) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for HSD17B1 at approximately 37 kDa. The expected band size for HSD17B1 is at 35 kDa.
IHC analysis of HSD17B1 using anti-HSD17B1 antibody (A02198) .
HSD17B1 was detected in a paraffin-embedded section of human placenta tissue. The tissue section was incubated with rabbit anti-HSD17B1 Antibody (A02198) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IF analysis of HSD17B1 using anti-HSD17B1 antibody (A02198).
HSD17B1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-HSD17B1 Antibody (A02198) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).
Western blot analysis of HSD17B1 using anti-HSD17B1 antibody (A02198). The sample well of each lane was loaded with 30 ug of sample under reducing conditions.
Lane 1: human placenta tissue lysates.
After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HSD17B1 antigen affinity purified polyclonal antibody (A02198) at a dilution of 1:1000 and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for HSD17B1 at approximately 37 kDa. The expected band size for HSD17B1 is at 35 kDa.
IHC analysis of HSD17B1 using anti-HSD17B1 antibody (A02198) .
HSD17B1 was detected in a paraffin-embedded section of human placenta tissue. The tissue section was incubated with rabbit anti-HSD17B1 Antibody (A02198) at a dilution of 1:200 and developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB (Catalog # AR1027) as the chromogen.
IF analysis of HSD17B1 using anti-HSD17B1 antibody (A02198).
HSD17B1 was detected in an immunocytochemical section of U2OS cells. The section was incubated with rabbit anti-HSD17B1 Antibody (A02198) at a dilution of 1:100. DyLight®488 Conjugated Goat Anti-Rabbit IgG (Green) (Catalog # BA1127) was used as secondary antibody. The section was counterstained with DAPI (Catalog # AR1176) (Blue).