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Fixation buffer

Manufactured by Cytek Biosciences

Fixation buffer is a laboratory reagent used to preserve the structural integrity of cells or tissues. It functions by chemically fixing and stabilizing cellular components, preventing degradation or morphological changes. The buffer composition and pH are designed to maintain the sample in a fixed state suitable for downstream analysis or processing.

Automatically generated - may contain errors

2 protocols using fixation buffer

1

Multiparameter Flow Cytometry Staining

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cells were stained in the presence of 1:500 Fc block (CD16/32, Tonbo) and antibodies diluted 1:200 in FACs buffer (PBS+2.5% FBS) for 45 minutes in the dark at 4°C. Ghost viability dye BV540 (Tonbo) was used to exclude dead cells at 1:500. Cells were fixed in 2% PFA or fixation buffer (Tonbo) for 10–15 at room temperature in the dark prior to data acquisition. Cells were acquired within 24 h using a Cytek Aurora.
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2

Multiparameter Flow Cytometry Staining

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cells were stained in the presence of 1:500 Fc block (CD16/32, Tonbo) and antibodies diluted 1:200 in FACs buffer (PBS+2.5% FBS) for 45 minutes in the dark at 4°C. Ghost viability dye BV540 (Tonbo) was used to exclude dead cells at 1:500. Cells were fixed in 2% PFA or fixation buffer (Tonbo) for 10–15 at room temperature in the dark prior to data acquisition. Cells were acquired within 24 h using a Cytek Aurora.
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