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Pe conjugated anti human cd45 antibody

Manufactured by BioLegend
Sourced in United States

The PE)-conjugated anti-human CD45 antibody is a laboratory reagent used for the detection and identification of human CD45-expressing cells. CD45 is a transmembrane protein tyrosine phosphatase that is expressed on the surface of most hematopoietic cells. The PE (Phycoerythrin) fluorescent dye is conjugated to the antibody, allowing for the detection and quantification of CD45-positive cells using flow cytometry or other fluorescence-based techniques.

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3 protocols using pe conjugated anti human cd45 antibody

1

Intravascular Labeling of Human Cells

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Human CD45+ hematopoietic cells in the blood and the organ vasculature of HSPC-engrafted MISTRG mice were labeled as previously described (31 (link)). For this purpose, 2 μg of a phycoerythrin (PE)-conjugated anti-human CD45 antibody (Biolegend, clone HI30) was injected intravenously (IV) 5 minutes before organ harvest without any prior perfusion. After isolation from various organs (bone marrow, spleen, liver, lung), cells were stained ex vivo with an APC-Cy7-conjugated anti-human CD45 antibody and other cell surface antibodies to determine the frequency of intravascular (IV CD45-PE+) and extravascular (IV CD45-PE-) ILCs by flow cytometry. Blood was also analyzed by flow cytometry to confirm successful intravascular labelling, defined as >90% IV CD45-PE+ human cells in blood.
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2

Intravascular Labeling of Lung Immune Cells

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HSPC-engrafted MISTRG mice were injected intravenously with 2 μg of PE-conjugated anti-human CD45 antibody (Biolegend, clone HI30) to label human hematopoietic cells in the blood and the lung vasculature. Mice were sacrificed 5 minutes after injection and lungs harvested without prior perfusion. Lung immune cells were isolated as above and stained with APC-Cy7-conjugated anti-human CD45 antibody and other antibodies ex vivo for flow cytometry as described below. As a positive and negative control, cells from blood and BAL fluid were used, respectively. Only lung samples from mice with successful intravascular labelling (>90% CD45-PE+ in blood) were used for analysis.
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3

Multicolor Flow Cytometry of Cells

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The following antibodies were used: purified rat anti‐mouse CD31 antibody (BD Pharmingen), Alexa 647‐conjugated anti‐mouse CD31 antibody, APC‐conjugated anti‐mouse CD45 antibody, purified mouse anti‐human CD31 antibody, Alexa 647‐conjugated anti‐human CD31 antibody, PE‐conjugated anti‐human CD45 antibody (BioLegend, San Diego, CA, USA), anti‐ALDH1A1 antibody (Abcam, Cambridge, UK), Alexa 594‐conjugated anti‐rabbit IgG, and Alexa Fluor 568‐conjugated anti‐rat IgG antibody (Invitrogen, Tokyo, Japan).
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