WB
Western blot analysis of lysates from SK-BR-3 cells, using HER2/ErbB2 Rabbit mAb at1:2000
dilution.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit.
Exposure time: 1s.
IHC
Immunohistochemistry analysis of paraffin
embedded Human breast cancer using
HER2/ErbB2 Rabbit mAb at dilution
of 1:200 (40x lens). High pressure antigen
retrieval performed with 0.01M Citrate buffer
(pH 6.0) prior to IHC staining.
IHC
The multiplex IHC analysis on paraffin
embedded Human breast cancer tissue using
the following specific primary antibodies and
tyramide signal amplification (TSA) reagents
: Ki67 Rabbit mAb (1:500) with TSA-TYR-520 (Green),
HER2/ErbB2 Rabbit mAb (1:200)
with TSA-TYR-570 (Red), and Androgen
Receptor Rabbit mAb (1:400) with
TSA-TYR-690 (Magenta). DAPI (Blue) was
used for nuclear staining. Prior to multiplex
IHC staining, high-pressure antigen retrieval
was performed using 0.01M citrate buffer at
pH 6.0. The analysis was completed using a
20x objective lens.
IF-P
Confocal imaging of paraffin-embedded
Human breast cancer tissue using
HER2/ErbB2 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.