WB
Western blot analysis of various lysates using TIM-1/KIM-1/HAVCR Rabbit mAb at 1:5000 dilution incubated
overnight at 4℃.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Negative control (NC): MEF.
Exposure time: 90 s.
IHC
Immunohistochemistry analysis of paraffin-embedded
Mouse kidney tissue using TIM-1/KIM-1/HAVCR Rabbit
mAb at a dilution of 1:7000 (40x lens). High
pressure antigen retrieval performed with 0.01M Tris
EDTA Buffer (pH 9.0) prior to IHC staining.
IP
Immunoprecipitation of TIM-1/KIM-1/HAVCR from 300 µg extracts of A20 cells was performed using 2 µg of TIM
1/KIM-1/HAVCR Rabbit mAb. Rabbit Control IgG was used to precipitate the Control IgG sample. IP
samples were eluted with 1x Laemmli Buffer. The Input lane represents 10% of the total input. Western blot analysis
of immunoprecipitates was conducted using TIM-1/KIM-1/HAVCR Rabbit mAb at a dilution of 1:1000.