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Leukoreduction filters

Manufactured by Haemonetics

Leukoreduction filters are medical devices used in blood processing laboratories. They are designed to remove white blood cells (leukocytes) from blood components, such as red blood cells or platelets, before transfusion or further processing. The core function of these filters is to reduce the number of leukocytes in the blood product, which can help minimize certain adverse reactions in patients receiving blood transfusions.

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2 protocols using leukoreduction filters

1

Isolation and Differentiation of Human Monocyte-Derived Macrophages

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Human PBMCs were isolated from leukoreduction filters (Haemonetics) obtained from healthy donors by density gradient centrifugation. Primary CD14+ monocytes were isolated from PBMCs using mouse anti‐human CD14 monoclonal antibody‐conjugated magnetic beads and LS MACS cell separation columns (Miltenyi Biotec) according to the manufacturer's protocol. Primary MDMs were generated by culturing CD14+ monocytes in RPMI‐1640 with 10% human AB serum, 10% FBS, 100 U/ml penicillin (Gibco), 100 μg/ml streptomycin (Gibco), and 0.29 mg/ml l‐glutamine (Gibco) for 6 days to differentiate into MDMs. Following differentiation, MDMs were cultured in RPMI‐1640 supplemented with 10% FBS, 100 U/ml penicillin, 100 μg/ml streptomycin, and 0.29 mg/ml l‐glutamine. The genetic sex of a subset of the donors was determined by PCR amplification of the SRY gene located on the Y chromosome. PM1 cells were cultured in RPMI‐1640 supplemented with 10% FBS, 100 U/ml penicillin, 100 μg/ml streptomycin, and 0.29 mg/ml l‐glutamine. 293T cells were cultured in DMEM supplemented with 10% FBS, 100 U/ml penicillin, 100 μg/ml streptomycin, and 0.29 mg/ml l‐glutamine.
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2

Isolation and Differentiation of Primary Human Monocytes

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human PBMCs were isolated from leukoreduction filters (Haemonetics) obtained from healthy donors by density gradient centrifugation. Primary CD14+ monocytes were isolated from PBMCs using mouse anti-human CD14 monoclonal antibody-conjugated magnetic beads and LS MACS cell separation columns (Miltenyi Biotec) according to the manufacturer’s protocol. Primary monocyte-derived macrophages (MDMs) were generated by culturing CD14+ monocytes in RPMI-1640 with 10% human AB serum, 10% FBS, 100 U/ml penicillin (Gibco), 100 μg/ml streptomycin (Gibco), and 0.29 mg/ml L-glutamine (Gibco) for six days to differentiate into MDMs. Following differentiation, MDMs were cultured in RPMI-1640 supplemented with 10% FBS, 100 U/ml penicillin, 100 μg/ml streptomycin, and 0.29 mg/ml L-glutamine. The genetic sex of a subset of the donors was determined by PCR amplification of the SRY gene located on the Y chromosome. PM1 cells were cultured in RPMI-1640 supplemented with 10% FBS, 100 U/ml penicillin, 100 μg/ml streptomycin, and 0.29 mg/ml L-glutamine. 293T cells were cultured in DMEM supplemented with 10% FBS, 100 U/ml penicillin, 100 μg/ml streptomycin, and 0.29 mg/ml L-glutamine.
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