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Cd68 rabbit polyclonal antibody

Manufactured by Abcam
Sourced in United States

The CD68 rabbit polyclonal antibody is a laboratory reagent used for the detection and analysis of the CD68 protein, which is a glycoprotein expressed on the surface of monocytes and macrophages. This antibody can be used in various immunoassay techniques to identify and study cells expressing the CD68 protein.

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4 protocols using cd68 rabbit polyclonal antibody

1

Antibody Validation for Breast Cancer

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The monoclonal antibody to human QTRT1 was purchased from Santa Cruz Biotechnology (Dallas, TX, USA). Monoclonal antibodies of β-catenin and E-cadherin from BD Transduction (San Jose, CA, USA) and β-actin were purchased from Sigma-Aldrich (St. Louis, MO, USA). Monoclonal antibodies of PCNA and CD11b (Integrin αM) were purchased from Santa Cruz Biotechnology (Dallas, TX, USA). Claudin-5 and claudin-2 mouse monoclonal antibodies and ZO-1 rabbit monoclonal antibody were purchased from Thermo Fisher Scientific (Rockford, IL, USA). CD68 rabbit polyclonal antibody was purchased from Abcam (Cambridge, MA, USA). All chemicals were purchased from Sigma-Aldrich unless otherwise stated. The breast cancer cell lines, including MCF7 and MDA-MB-231, were provided by Dr. Tao Pan’s lab at the University of Chicago.
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2

Antibody Characterization in Breast Cancer

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The monoclonal antibody to human QTRT1 was purchased from Santa Cruz Biotechnology (Dallas, TX). Monoclonal antibody of β-catenin and E-cadherin from BD Transduction (San Jose, CA), and β-actin were purchased from Sigma-Aldrich (St. Louis, MO). Monoclonal antibody of PCNA and CD11b (Integrin αM) were purchased from Santa Cruz Biotechnology (Dallas, TX). Claudin 5 and Claudin 2 mouse monoclonal antibody and ZO-1 rabbit monoclonal antibody were purchased from Thermo Fisher Scienti c (Rockford, IL). CD68 rabbit polyclonal antibody was purchased from Abcam (Cambridge, MA). All chemicals were purchased from Sigma-Aldrich unless otherwise stated. The breast cancer cell lines, including MCF7 and MDA-MB-231, were provided by Dr. Tao Pan's lab at University of Chicago.
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3

Histological and Immunohistochemical Staining Protocol

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Five-micron sections were deparaffinized and rehydrated in the following order for histological and immunohistochemical staining: three washes of xylene, 100% ethanol, 90% ethanol, 70% ethanol, and two washes of Tris-buffered vehicle. Slides were stained with hematoxylin and eosin for evaluation of morphology and picrosirius red to detect fibrillar collagen. Immunohistochemistry was performed using rat anti-mouse CD45 antibody (BD Biosciences), rabbit polyclonal CD68 antibody (Abcam), rabbit anti-mouse vimentin antibody (Cell Signaling), rabbit anti-mouse α-smooth muscle actin antibody (Abcam), anti-pan keratin antibody (Abcam), rabbit anti-collagen I antibody (Abcam), rabbit anti-collagen III antibody (Abcam), rabbit anti-FBN antibody (Abcam), and goat anti-mouse DCN antibody (R&D Systems, Minneapolis, MN, USA) as described previously10 (link). Histological evaluation was performed independently by two experimental pathologists who were blinded to the experimental conditions.
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4

Immunohistochemical Analysis of Hippocampal Microglia

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Fixed brain tissue samples were used for immunohistochemistry as described previously (28, 29) . Briefly, hippocampal sections were incubated with either 1:500 rabbit polyclonal CD68 antibody (Abcam, Cambridge, UK) or 1:1000 recombinant anti-Iba1 antibody (Abcam, Cambridge, UK) overnight at 4 o C. Immunoreactivity was developed using Novolink polymer Detection Kit (Leica Biosystems, Buffalo Grove, IL) according to the manufacturer's protocol. Images were taken using OLYMPUS CX41 light microscope (Olympus, Shinjuku, Tokyo, Japan).
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