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Confirm anti er sp1

Manufactured by Roche
Sourced in Japan

The CONFIRM anti‐ER [SP1] is a laboratory equipment product manufactured by Roche. It is used for the detection and quantification of estrogen receptor (ER) in human breast cancer tissue samples. The product functions by providing an automated and standardized method for the analysis of ER expression levels, which is a crucial biomarker in the diagnosis and management of breast cancer.

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5 protocols using confirm anti er sp1

1

Immunohistochemical Analysis of CYC1, ER, PR, and HER2

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Rabbit polyclonal antibody for CYC1 (PA5‐25257) and mouse mAb for Ki‐67 (MIB1) were purchased from Thermo Fisher Scientific (Waltham, MA, USA) and Dako (Carpinteria, CA, USA), respectively. The antigen–antibody complex was visualized with DAB solution and counterstained with hematoxylin. We used human tissue of the stomach as a positive control based on a data sheet of CYC1 antibody by Novus Biologicals (http://www.novusbio.com/CYC1-Antibody_NBP1-86872.html#dsTab0) and normal rabbit IgG instead of the primary antibody as a negative control for CYC1 immunostaining in this study.
Immunohistochemistry for ER (CONFIRM anti‐ER [SP1]; Roche Diagnostics Japan, Tokyo, Japan) and PR (CONFIRM anti‐PR [1E2]; Roche Diagnostics Japan) was carried out with Ventana Benchmark XT (Roche Diagnostics Japan), and that for HER2 was carried out using HercepTest (Dako).
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2

Immunohistochemical Analysis of Breast Cancer Markers

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Rabbit polyclonal antibody for TACC2 (GTX110516) and mouse monoclonal antibodies for Ki‐67 (MIB1) and androgen receptor (AR; AR441) were purchased from Gene Tex (Hsinchu, Taiwan ROC), DAKO (Carpinteria, CA) and DAKO, respectively. A Histofine Kit (Nichirei Biosciences, Tokyo, Japan), which employs the method of streptavidin‐biotin amplification was used in this study. The visualization of antigen–antibody complex was possible with 3,3′‐diaminobenzidine (DAB) solution and after that counterstained with hematoxylin. As a positive control for TACC2 immunostaining, human prostate carcinoma tissue was used 10. Immunohistochemistry for estrogen receptor (ER) (CONFIRM anti‐ER (SP1)) and progesterone receptor (PR) (CONFIRM anti‐PR (1E2); Roche Diagnostics, Tokyo, Japan) was performed with Ventana Benchmark XT (Roche Diagnostics), and that for HER2 was performed by HercepTest (DAKO). Ki‐67 (MIB1) was purchased from DAKO, and a Histofine Kit (Nichirei Bioscience, Tokyo, Japan) was used for the immunohistochemistry.
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Standardized ER Assessment of Liver Metastases

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According to standard clinical care procedures, all ultrasound-guided percutaneous 18G core needle liver biopsies were performed by experienced abdominal radiologists. ER status of the liver metastasis was determined by staining the formalin-fixed paraffin-embedded liver biopsies using the CONFIRM anti-ER (SP1, Roche) on an automated Benchmark Ultra platform (Roche). Metastases were deemed ER+ if ≥10% of the tumor cells showed nuclear staining, according to Dutch guidelines. The immunohistochemical evaluation of the ER status was used as the reference standard.
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4

Immunohistochemical Profiling of Breast Cancer

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Mouse monoclonal antibodies for CITED2 (LS‐B243) and Ki‐67 (MIB1) were purchased from LSBio (Seattle, WA, USA) and Dako (Carpinteria, CA, USA), respectively. The antigen–antibody complex was visualized with 3,3′‐diaminobenzidine solution and counterstained with hematoxylin. Immunohistochemistry for ER (CONFIRM anti‐ER [SP1]) and progesterone receptor (PR) (CONFIRM anti‐PR [1E2]; Roche Diagnostics Japan, Tokyo, Japan) was performed with Ventana Benchmark XT (Roche Diagnostics Japan), and that for HER2 was performed by HercepTest (Dako).
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5

Immunohistochemical Evaluation of Biomarkers

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Rabbit polyclonal antibodies for OLFM4 (ab96280) and LY6D (HPA024755) and mouse monoclonal antibody for S100A7 (47C1068) were purchased from Abcam (Cambridge, UK), Sigma‐Aldrich (St. Louis, MO, USA) and LifeSpan BioSciences (Seattle, WA, USA), respectively. Immunostaining for these 3 antibodies was automatically performed using Ventana Benchmark XT platform (Roche Diagnostics Japan, Tokyo, Japan). As a positive control, we used human tissue of the prostate, skin and skin for OLFM4, LY6D and S100A7, respectively, based on the data sheet (OLFM4) and database of the Human Protein Atlas (https://www.proteinatlas.org) (LY6D and S100A7).
Immunohistochemistry for ER (CONFIRM anti‐ER [SP1]) and progesterone receptor (PR) (CONFIRM anti‐PR [1E2]; Roche Diagnostics Japan) was also performed with Ventana Benchmark XT (Roche Diagnostics Japan), and that for HER2 was performed by HercepTest (DAKO). Mouse monoclonal antibody for Ki67 (MIB1) was purchased from DAKO (Carpinteria, CA, USA), and a Histofine kit (Nichirei Bioscience, Tokyo, Japan) was used for the immunohistochemistry.
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