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Sc 26643 r

Manufactured by Santa Cruz Biotechnology

Sc-26643-R is a laboratory product designed for research purposes. It is a solution that can be used for various applications in a laboratory setting. The core function of this product is to facilitate specific research activities, but a detailed description cannot be provided while maintaining an unbiased and factual approach.

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2 protocols using sc 26643 r

1

Immunohistochemical Analysis of Colon Tissues

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Colon tissues were fixed in 4% paraformaldehyde and embedded in paraffin. After incubation with blocking buffer, the sections were incubated with a goat polyclonal antivimentin antibody (sc-7557, 1:50 dilution; Santa Cruz Biotechnology, Santa Cruz, CA), a rabbit polyclonal anti-F4/80 antibody (sc-26643-R, 1:50 dilution; Santa Cruz Biotechnology), or a rabbit polyclonal anti-phospho-ERK antibody (no. 4370, 1:50 dilution; Cell Signaling Technologies, Danvers, MA) overnight at 4°C. After washing, the sections were incubated with donkey anti-goat IgG or bovine anti-rabbit IgG, and the slides were stained with an ABC kit for color development (sc-2018; Santa Cruz Biotechnology). Immunohistochemistry was assisted by Translational Pathology Core Laboratory (TPCL) of UCLA. Images were analyzed with a Zeiss AX10 microscope at magnification of 200×.
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2

Immunohistochemical Analysis of Colon Tissue

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Colon tissues were fixed in 4% paraformaldehyde and embedded in paraffin. After incubation with blocking buffer, sections were incubated with a goat polyclonal anti-vimentin antibody (sc-7557, Santa Cruz biotechnology, Santa Cruz, CA, 1:50 dilution), a rabbit polyclonal anti-F4/80 antibody (sc-26643-R, Santa Cruz, 1:50 dilution) or a rabbit polyclonal anti-phospho-ERK antibody (#4370, Cell signaling, Danvers, MA, 1:50 dilution) overnight at 4°C. After washing, sections were incubated with donkey anti-goat IgG or bovine anti-rabbit IgG and slides were stained with an ABC kit for color development (Santa Cruz, sc-2018). Immunohistochemistry was assisted by Translational Pathology Core Laboratory (TPCL) of UCLA. Images were analyzed with a Zeiss AX10 microscope at magnification of 200×.
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