WB
Western blot analysis of various lysates using Nectin-4 Rabbit mAb at 1:5000 dilution incubated
overnight at 4℃. T-47D cells were treated with PNGase F (2 U/μL) at 37℃ for 1 hour.
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.
Negative control (NC): U-937.
Exposure time: 90 s.
IHC
Immunohistochemistry analysis of paraffin
embedded Human esophagus tissue using
Nectin-4 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.
IHC
Immunohistochemistry analysis of paraffin
embedded Mouse esophagus tissue using
Nectin-4 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.
IHC
Immunohistochemistry analysis of paraffin
embedded Rat esophagus tissue using
Nectin-4 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 MCF7 cells using
Nectin-4 Rabbit mAb (dilution
1:200) followed by a further incubation with
Cy3-conjugated Goat anti-Rabbit IgG (H+L)
(dilution 1:500) (Red). The cells were
counterstained with α-Tubulin Mouse mAb
(dilution 1:400) followed by
incubation with 488-conjugated Goat
Anti-Mouse IgG (H+L) Ab (dilution
1:500) (Green). DAPI was used for nuclear
staining (Blue). Objective: 100x.
IF-P
Confocal imaging of paraffin-embedded
Mouse esophagus tissue using Nectin-4
Rabbit mAb (dilution 1:200)
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). High pressure
antigen retrieval performed with 0.01M
Citrate Buffer (pH 6.0) prior to IF staining.
Objective: 40x.