WB
Western blot analysis of various lysates using CXCL10/IP-10 Rabbit mAb at 1:10000
dilution incubated overnight at 4℃. A549 cells and HT-29 cells were treated with TNF-α (20ng/mL) for 6
hours, Brefeldin A (300ng/mL) for 3 hours and IFN-γ (50ng/mL) for 8 hours.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 30 μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 5s.
IHC
Immunohistochemistry analysis of paraffin
embedded Human tonsil tissue using
CXCL10/IP-10 Rabbit mAb at a
dilution of 1:500 (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 THP-1 cells (treated with
IFN-γ, LPS and BFA) and THP-1 cells
(untreated) using CXCL10/IP-10 Rabbit mAb
(dilution 1:200) followed by a
further incubation with Cy3 Goat Anti-Rabbit
IgG (H+L) (dilution 1:500) (Red).
DAPI was used for nuclear staining (Blue).
Objective: 100x.