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Apc conjugated anti mouse secondary antibodies

Manufactured by Jackson ImmunoResearch
Sourced in United States

APC conjugated anti-mouse secondary antibodies are used to detect the presence of mouse primary antibodies in various immunoassay techniques. The APC (Allophycocyanin) fluorescent dye is conjugated to the anti-mouse secondary antibody, allowing for the visualization and quantification of the target mouse antibodies.

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2 protocols using apc conjugated anti mouse secondary antibodies

1

Triple Immunofluorescent Staining of Telocytes

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Triple immunofluorescent staining for CD34/Vimentin/PDGFRα was used as previously reported [17 (link), 18 (link)]. In brief, TCs were cultured on glass bottom cell culture dishes with 20 mm diameter glass (NEST, Nanjing, China) and were fixed in 4% paraformaldehyde containing 0.05% Triton-X-100 for 20 min. Then washed the dishes three times wash with 1 × PBS and blocked in 5% Bovine serum albumin (BSA) for 1 h. After incubated overnight at 4 °C with mouse anti-CD34 antibody, goat anti-vimentin antibody or rat anti- PDGFRα antibody (1:200 dilution; Abcam, Cambridge, UK) diluted in 1% bovine serum albumin (BSA) in PBS, the dishes were washing in PBS for three times. Then, dishes were incubated with APC conjugated anti-mouse secondary antibodies, PE conjugated anti-rat secondary antibodies and FITC conjugated anti-goat secondary antibodies (1:200 dilution; Jackson ImmunoResearch, USA). The nuclear were marked by DAPI according to the manufacture (KeyGEN BioTECH, Nanjing, China). Cells were observed and recorded under Olympus FV3000 Confocal Laser Scanning Microscope (DSS Imagetech Pvt. Ltd, New Delhi, India).
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2

Immunofluorescent Staining for TC Identification

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Immunofluorescent staining for CD34/Vimentin/PDGFα was used as previously reported for TCs identification. In brief, TCs were seeded on glass bottom cell culture dishes with 15 mm diameter glass (NEST, Nanjing, China) overnight. Then, cells were fixed in 4% paraformaldehyde containing 0.05% Triton-X-100 for 20 min and the dishes were washed for three times with 1 × PBS before blocking in 5% Bovine serum albumin (BSA) for 1 h. After incubated with mouse anti-CD34 antibody, goat anti-vimentin antibody or rat anti- PDGFRα antibody (1:200 dilution; Abcam, Cambridge, UK) diluted in 1% bovine serum albumin (BSA) in PBS overnight at 4 °C, the dishes were washing in PBS for three times. Cells were incubated with APC conjugated anti-mouse secondary antibodies, PE conjugated anti-rat secondary antibodies and FITC conjugated anti-goat secondary antibodies (1:200 dilution; Jackson ImmunoResearch, USA) for other 1 h at 4 °C in dark. The nuclear were marked with DAPI according to the manufacture (KeyGEN BioTECH, Nanjing, China). TCs were observed and recorded using Olympus FV3000 Confocal Laser Scanning Microscope (DSS Imagetech Pvt. Ltd, New Delhi, India).
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