Immunohistochemical staining for CD10, B-cell lymphoma 6 (BCL-6) and Multiple myeloma antigen 1 (MUM1) in the tissue was performed. The sections were incubated with 3% H 2 O 2 at room temperature for 10 minutes and then washed with phosphate buffer saline (PBS). Next, the sections were stained for the following antibodies: CD10 (ZM0283, ZSGB-BIO, CA, USA), BCL-6 (ZM-0011, ZSGB-BIO, CA, USA) and MUM1(ZM0039, ZSGB-BIO, CA, USA) at 4 ℃ overnight. After washing in PBS again, the sections were incubated with secondary antibodies (PV6000, ZSGB-BIO, CA, USA). Finally, the reactivity was visualized by diaminobenzidine (DAB). The staining intensity and percentage of positive cells were recorded. Immunohistochemical analysis was independently reviewed by at least two experienced tissue pathologists.
Zm 0011
Manufactured by ZSGB-BIO
Sourced in United States
The ZM-0011 is a high-precision laboratory centrifuge designed for a variety of applications. It features a powerful motor and a robust construction to ensure reliable and consistent performance. The centrifuge can achieve speeds up to 15,000 RPM, making it suitable for a wide range of sample processing needs. The device is equipped with a multi-functional display and intuitive controls for easy operation.
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Lab products found in correlation
2 protocols using zm 0011
1
Immunohistochemical Profiling of Lymphoma Markers
2
Immunohistochemical Profiling of Lymphoma Markers
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Immunohistochemical staining for CD10, B-cell lymphoma 6 (BCL-6) and Multiple myeloma antigen 1 (MUM1) in the tissue was performed. The sections were incubated with 3% H 2 O 2 at room temperature for 10 minutes and then washed with phosphate buffer saline (PBS). Next, the sections were stained for the following antibodies: CD10 (ZM0283, ZSGB-BIO, CA, USA), BCL-6 (ZM-0011, ZSGB-BIO, CA, USA) and MUM1(ZM0039, ZSGB-BIO, CA, USA) at 4 ℃ overnight. After washing in PBS again, the sections were incubated with secondary antibodies (PV6000, ZSGB-BIO, CA, USA). Finally, the reactivity was visualized by diaminobenzidine (DAB). The staining intensity and percentage of positive cells were recorded. Immunohistochemical analysis was independently reviewed by at least two experienced tissue pathologists.
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