IHC
Immunohistochemistry analysis of paraffin
embedded Rat spleen tissue using ZO-1
Rabbit mAb at a dilution of 1:1000
(40x lens). High pressure antigen retrieval
was performed with 0.01 M citrate buffer (pH
6.0) prior to IHC staining
IHC
Immunohistochemistry analysis of paraffin
embedded Mouse intestine tissue using ZO-1
Rabbit mAb at a dilution of 1:800
(40x lens). High pressure antigen retrieval
performed with 0.01M Tris-EDTA Buffer (pH
9.0) prior to IHC staining.
IF-P
Confocal imaging of paraffin-embedded
Mouse kidney tissue using ZO-1 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).
High pressure antigen retrieval performed
with 0.01M Citrate Buffer(pH 6.0) prior to IF
staining. Objective: 40x.
IF-P
Confocal imaging of paraffin-embedded Rat
spleen tissue using ZO-1 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).
High pressure antigen retrieval performed
with 0.01M Citrate Buffer(pH 6.0) prior to IF
staining. Objective: 40x.
ICC/IF
Confocal imaging of MCF7 cells using ZO-1
Rabbit mAb (dilution 1:100)
followed by a further incubation with Cy3
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.