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Her2 erbb2 d8f12 xp rabbit mab

Manufactured by Cell Signaling Technology
Sourced in United States

The HER2/ErbB2 (D8F12) XP TM rabbit mAb is a primary antibody designed for the detection of HER2/ErbB2 protein expression. It is produced using recombinant technology and purified from mammalian cell culture supernatant.

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2 protocols using her2 erbb2 d8f12 xp rabbit mab

1

Immunofluorescence Staining of Breast Cancer Cells

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Prior to ICC, coverslips needed to be put at the bottom of the wells in a 24-well plate. In total, 1 × 105 HER2-positive breast cancer cells (SK-BR3, MDA-MB361, and JIMT1) and HER2-negative breast cancer cells (MCF7) were seeded on the coverslips. Cells were fixed in 4% paraformaldehyde for 15 min and washed with phosphate-buffered saline (PBS) twice. Nonspecific sites were then blocked with 3% bovine serum albumin (BSA, Sigma-Aldrich, Burlington, MA, USA) in PBS for 30 min at room temperature. Cells were incubated with anti-HER2 antibody (HER2/ErbB2 (D8F12) XP TM rabbit mAb, Cell Signaling Technology, Danvers, MA, USA) overnight at 4 °C and washed with PBS, followed by incubation with the appropriate Alexa Fluor 488 secondary antibody (1:1000, anti-rabbit IgG Fab2, Alexa Fluor ® 488, Cell Signaling Technology, Danvers, MA, USA) for 1 h at room temperature. The coverslips were added to the mounting medium with DAPI (Vectashield Mounting Medium with DAPI, Tokyo, Japan) for 10 min and were observed using a fluorescence microscope (LSM 700 confocal, ZEISS, Oberkochen, Germany).
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2

HER2 Expression Imaging in Breast Cancer

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In total, 1 × 105 HER2-overexpressing breast cancer cells (SK-BR3, BT474, MDA-MB361) and HER2 low-expressing breast cancer cells (MDA-MB231, MDA-MB468) were seeded on coverslips at the bottoms of wells in a 24 well-plate. Cells were fixed in 4% paraformaldehyde for 15 min, washed with phosphate-buffered saline (PBS) twice, and non-specific sites were blocked with 3% bovine serum albumin (BSA) in PBS for 30 min at room temperature. Cells were incubated with anti-HER2 antibody (HER2/ErbB2 (D8F12) XPTM Rabbit mAb, Cell Signaling technology, Danvers, MA, USA) overnight at 4 °C, followed by incubation with the appropriate Alexa Fluor 488 secondary antibody (1:1000, Anti-Rabbit IgG Fab2, Alexa Fluor (R) 488, Cell Signaling technology) for 1 h at room temperature. The cover slips were added the mounting medium with DAPI for 10 min prior to imaging by fluorescence microscope (LSM 700 confocal, ZEISS, Oberkochen, Germany).
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