WB
Western blot analysis of lysates from Rat adipose using ATGL/PNPLA2 Rabbit mAb at 1:15000
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.
Exposure time: 20 s.
WB
Western blot analysis of various lysates using ATGL/PNPLA2 Rabbit mAb at 1:15000 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.
Exposure time: 20 s.
IHC
Immunohistochemistry analysis of paraffin
embedded Mouse brown adipose tissue
using ATGL/PNPLA2 Rabbit mAb at
a dilution of 1:5000 (40x lens). High pressure
antigen retrieval performed with 0.01M Tris
EDTA Buffer (pH 9.0) prior to IHC staining.
IHC
Immunohistochemistry analysis of paraffin
embedded Rat brown adipose tissue using
ATGL/PNPLA2 Rabbit mAb at a
dilution of 1:5000 (40x lens). High pressure
antigen retrieval performed with 0.01M Tris
EDTA Buffer (pH 9.0) prior to IHC staining.
ICC/IF
Confocal imaging of 3T3-L1 differentiated
cells and 3T3-L1 cells using ATGL/PNPLA2
Rabbit mAb (dilution 1:400)
followed by a further incubation with Cy3
conjugated Goat anti-Rabbit IgG (H+L)
(dilution 1:500) (Red). DAPI was used
for nuclear staining (Blue). Objective: 100x.