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Rat anti mouse cd140b clone apb5

Manufactured by Thermo Fisher Scientific

The Rat anti-mouse CD140B (clone APB5) is a monoclonal antibody that binds to the mouse CD140B protein, also known as platelet-derived growth factor receptor beta (PDGFRB). This antibody can be used to detect and analyze CD140B-expressing cells in various applications, such as flow cytometry and immunohistochemistry.

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2 protocols using rat anti mouse cd140b clone apb5

1

Tissue Preparation and Immunostaining Protocol

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To generate tissues for immunostaining, mice were transcardially perfused with DPBS to remove blood, then perfused with 4% paraformaldehyde in PBS, the tissues were dissected and cryopreserved in 30% sucrose, frozen in 2:1 30%sucrose:OCT and then 10 micron sections were generated. For immunostaining, tissue sections were blocked/permeabilized with 0.1–5% Triton X-100 and 10–50% goat serum in PBS. Tissue sections were incubated in primary antibodies overnight at 4°C and secondary antibodies for 1.5 hours at room temperature with 3% goat serum, 0–0.1% Triton X-100 in PBS. Primary antibodies (1/500 dilution): rat anti-mouse CD31 (clone MEC13.3, BD Pharmingen 553370), rat anti-mouse CD45 (clone YW62.3, BioRad MCA1031GA), rat anti-mouse CD140B (clone APB5, eBiosciences 14–1402-82), rabbit anti Fibrinogen (Abcam ab34269), rabbit anti Claudin 5 (Life Technologies 341600), rabbit anti Collagen I (Abcam ab21286), rabbit anti Collagen III (Abcam ab7778), rabbit anti Decorin (Biomatik CAC07220), rabbit anti Lumican (Biomatik CAU25816), rabbit anti SPP1 (Abcam ab8448). Secondary antibodies (1/1000 dilution): Life Technologies goat anti-mouse alexa-594, goat anti-rat alexa-488 and alexa-594, goat anti-rabbit alexa-594. DAPI for nuclear labeling.
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2

Tissue Preparation and Immunostaining Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
To generate tissues for immunostaining, mice were transcardially perfused with DPBS to remove blood, then perfused with 4% paraformaldehyde in PBS, the tissues were dissected and cryopreserved in 30% sucrose, frozen in 2:1 30%sucrose:OCT and then 10 micron sections were generated. For immunostaining, tissue sections were blocked/permeabilized with 0.1–5% Triton X-100 and 10–50% goat serum in PBS. Tissue sections were incubated in primary antibodies overnight at 4°C and secondary antibodies for 1.5 hours at room temperature with 3% goat serum, 0–0.1% Triton X-100 in PBS. Primary antibodies (1/500 dilution): rat anti-mouse CD31 (clone MEC13.3, BD Pharmingen 553370), rat anti-mouse CD45 (clone YW62.3, BioRad MCA1031GA), rat anti-mouse CD140B (clone APB5, eBiosciences 14–1402-82), rabbit anti Fibrinogen (Abcam ab34269), rabbit anti Claudin 5 (Life Technologies 341600), rabbit anti Collagen I (Abcam ab21286), rabbit anti Collagen III (Abcam ab7778), rabbit anti Decorin (Biomatik CAC07220), rabbit anti Lumican (Biomatik CAU25816), rabbit anti SPP1 (Abcam ab8448). Secondary antibodies (1/1000 dilution): Life Technologies goat anti-mouse alexa-594, goat anti-rat alexa-488 and alexa-594, goat anti-rabbit alexa-594. DAPI for nuclear labeling.
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