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Blood can be processed in various ways to obtain cell preparations, which can then be used directly in biological assays or further processed to isolate more specific cell subsets. Common techniques include red blood cell lysis, density gradient centrifugation, and immunomagnetic cell separation (e.g. using �������⳧���™ technology), with each technique offering different advantages depending on the application.

Deplete Red Blood Cells

Isolation of specific cell types for functional studies or downstream assays may require RBC depletion during the cell preparation step. There are several ways to deplete RBCs, including:

• RBC lysis with ammonium chloride
• Dextran sedimentation or ���ٲ������™
• Immunomagnetic depletion with �������⳧���™ (e.g. �������⳧���™ RBC Depletion Reagent)
• Hypotonic lysis

After the RBC depletion is complete, the resulting sample will contain all nucleated white blood cells (leukocytes) that can be used for downstream assays or further processed to isolate a specific cell subset.

Prepare Peripheral Blood Mononuclear Cells

PBMCs include lymphocytes (i.e. T cells, B cells, and NK cells), monocytes, and dendritic cells, and are defined as white blood cells with round nuclei. Preparation of a PBMC fraction from whole blood is a common step prior to the isolation of specific immune cell subsets. The most common PBMC isolation method involves using a density gradient medium (e.g. ���⳾���DZ�����™ or Ficoll™) and centrifugation. This method takes advantage of the differences in density between the cells in blood and the density gradient medium.

Learn more about PBMCs, including their applications in research, in our Overview of Human Peripheral Blood Mononuclear Cells.

Tip: This process can be time consuming, particularly when working with multiple samples. To significantly speed up your PBMC isolations, use �����Ѳ��ٱ�™ tubes.

PBMCs can also be easily isolated directly from blood without centrifugation or lysis using the �������⳧���™ Direct Human PBMC Isolation Kit. This simple and fast immunomagnetic isolation method results in purified PBMCs in as little as 20 minutes from whole blood, cord blood, bone marrow, buffy coats, or leukapheresis products. Explore the benefits of �������⳧���™ Direct and see how it compares to traditional isolation methods. Need to obtain a large number of highly purified PBMCs quickly and reproducibly? Automate your PBMC isolations with ��Dz��dz����™ to save time and minimize manual handling. Alternatively, you can purchase frozen PBMCs.

After obtaining PBMCs, specific cell subsets can be isolated by using �������⳧���™ and other cell isolation techniques.

Prepare Peripheral Blood Polymorphonuclear Cells

Polymorphonuclear cells, also known as granulocytes, are a collection of immune cell subsets with enzyme-containing granules that can be released upon cell activation. To obtain a population of polymorphonuclear cells from whole blood, you can do either of the following:

• Perform density gradient centrifugation followed by ammonium chloride lysis. You can then isolate specific granulocyte populations such as neutrophils, basophils, or eosinophils using immunomagnetic cell separation technologies.
• Directly isolate granulocytes from blood, without lysis or density centrifugation, using �������⳧���™ Direct cell isolation technology. This approach allows you to quickly and easily obtain pan-granulocytes or one of the more specific granulocyte subsets (e.g. neutrophils, basophils, or eosinophils).
  

Prepare Buffy Coats

A buffy coat is a concentrated suspension of leukocytes that forms when erythrocytes and plasma are separated from the leukocyte fraction by low speed centrifugation.

Learn how to generate a buffy coat >

This procedure allows you to concentrate large sample volumes and remove donor-specific soluble serum factors, which helps to reduce donor variability. A buffy coat can be prepared from whole blood or bone marrow and can be used as the starting sample for the isolation of specific cell populations using immunomagnetic cell separation technologies such as �������⳧���™.

Isolate Specific Cell Subsets Directly from Whole Blood

Some cell separation technologies (e.g. �������⳧���™ Direct and ��Dz���ٳٱ𳧱��™) allow you to isolate specific cell subsets directly from whole blood without needing to isolate PBMCs first. To help streamline your cell isolation workflow and improve consistency, ��Dz��dz����™ instruments, powered by �������⳧���™ technology, enable fully automated, high-throughput isolation of specific cell subsets, minimizing sample handling and cross-contamination risk while delivering reliable, high-purity results with as little as 5 minutes of hands-on time.

Isolate Cells from Apheresis Products

Apheresis is a process in which whole blood is drawn from an individual, separated into components, and reinfused back into the individual with a certain component (e.g. plasma, platelets, or leukocytes) removed.

Leukapheresis is a form of apheresis where leukocytes are collected from a donor's circulating blood. Leukopaks, which are enriched leukapheresis products containing higher concentrations of leukocytes per volume compared to whole blood or buffy coat, are an ideal starting source of mononuclear cells that can be used for immune cell isolation. Depending on the method you choose, you can prepare a leukopak for cell separation by either isolating the PBMC fraction from it or simply depleting RBCs prior to cell isolation.

To easily isolate PBMCs or different cell subsets manually from large-volume samples, including leukopaks and whole blood, choose the Easy 250 �������⳧���™ Magnet with �������⳧���™ reagents to scale up your isolations with ease. Instead of splitting your cell suspension and performing multiple rounds of isolation, you can process samples of up to 225 mL and 12.5 × 10⁹ cells in as little as 20 minutes with a single isolation.

Plateletpheresis is another form of apheresis where thrombocytes, commonly called platelets, are separated from the rest of the blood. This process can include a leukoreduction step to remove leukocytes from the platelet fraction, resulting in leukocyte reduction system chambers/cones containing a high concentration of leukocytes in a small volume. LRSCs are usually discarded after routine donor plateletpheresis, but are an excellent source of leukocytes that can be used as an alternative source of PBMCs for research purposes.

Isolate Cells from Cord Blood

Cord blood can be collected from the placenta and umbilical cord after birth. Immune cells found in cord blood can be isolated to study early-life immune responses. To isolate specific cell populations from cord blood, you can first prepare mononuclear cells by using a density gradient medium (e.g. ���⳾���DZ�����™) and centrifugation, or you can simply deplete RBCs.

Depleting RBCs from cord blood requires special considerations. Standard ammonium chloride lysis may be too harsh for the hematopoietic or immune progenitor cells contained in cord blood. Alternative methods for RBC depletion may be better suited to removing RBCs from this sample source (e.g. �������⳧���™, ���ٲ������™).

Another factor to keep in mind is that cord blood can have very high platelet counts, which may facilitate the formation of clots. It is important to use suitable anticoagulants, like acid citrate dextrose (ACD) or EDTA, and to follow the manufacturer's instructions pertaining to cord blood when processing samples.

Learn about the isolation of CD34+ cells from human cord blood >