The authors would like to thank Nancy Mora for her technical assistance.
This work was funded by research grants 48573-M and 168098 from Consejo Nacional de Ciencia y Tecnologia, Mexico, and by grants IN212308 and IN205311-2 from Direccion General de Asuntos del Personal Academico, Universidad Nacional Autonoma de Mexico, Mexico.

1. Isolation of Neutrophils (PMN) from Human Blood
<ol>
	<li>Use about 20 ml human blood with heparin (10 U/ml) as anticoagulant. Blood was collected from adult healthy volunteers by venopuncture. All experiments were done under approval of the Bioethics Committee at the Instituto de Investigaciones Biom&eacute;dicas - UNAM.</li>
	<li>Put 2 ml of 6% dextran T500 in PBS into a 15 ml conical centrifuge tube and add 10 ml of blood. Mix by inverting the tube two or three times and let it sit for 45 min to allow for erythrocyte sedimentation.</li>
	<li>In a fresh 15 ml conical centrifuge tube put 5 ml Ficoll-Paque.</li>
	<li>Take the leukocyte-rich plasma that formed above sedimented erythrocytes, and carefully pipette it on top of the Ficoll-Paque forming a second layer. Make sure there are two phases.</li>
	<li>Centrifuge at 516 x g for 20 min at 4 &deg;C. After centrifugation, at the interphase of plasma and Ficoll-Paque there is a layer of mononuclear cells. Neutrophils are at the bottom of the tube.</li>
	<li>Eliminate the supernatant, break the cell pellet by tapping the tube against a rack, and resuspend the cells by adding 10 ml of cold (4 &deg;C) PBS. Note: Resuspending the cells by pipetting up and down is not recommended since this is too damaging to the cells.</li>
	<li>Transfer the cell suspension to a 50 ml conical centrifuge tube and centrifuge at 290 x g for 5 min at 4 &deg;C.</li>
	<li>Break the cell pellet as before and add 10 ml of cold (4 &deg;C) hypotonic solution (0.2% NaCl, 1% BSA, 20 mM Hepes, pH = 7.4) to lyse erythrocytes. Mix by swirling the tube gently by hand for exactly one minute.</li>
	<li>Add 10 ml of cold (4 &deg;C) hypertonic solution (1.6% NaCl, 1% BSA, 20 mM HEPES, pH = 7.4), mix and count the cells using a hemocytometer (usually &gt;95% are PMN). 
	Note: Keep the tube with the cell suspension on ice while counting the cells.</li>
	<li>Centrifuge as before and resuspend PMN at 107 cell/ml in cold (4 &deg;C) PBS. Keep on ice. 
	Note: Neutrophils remain viable and functional at 4 &deg;C for about 6 to 8 hr.</li>
</ol>
2. Activating PMN
<ol>
	<li>Put 100 &mu;l of PMN suspension (1 x 107cell/ml) into a 1.5 ml Eppendorf tube. 
	Note: Sample tubes should be done at least in duplicates. Usual negative controls should include first antibody only, and secondary antibody only.</li>
	<li>Add the corresponding anti-integrin or anti-Fc receptor monoclonal antibody (mAb) at 10 &mu;g/ml and incubate on ice for 15 min.</li>
	<li>Wash PMN by adding 1 ml of cold (4 &deg;C) PBS, centrifuging at 1,743 x g (4,500 rpm) in a microcentrifuge, and aspirating the supernatant.</li>
	<li>Break the cell pellet by tapping the bottom of the tube against a rack, add 1 ml cold PBS, and wash two more times as in previous step. 
	Note: These washes remove unbound antibody.</li>
	<li>Resuspend PMN in same (initial) volume of warm (37 &deg;C) PBS containing 60 &mu;g/ml of F(ab')2 goat anti-mouse IgG. 
	Note: The secondary anti-mouse IgG antibody will bind to the first anti-receptor antibody and will cause crosslinking of the receptor.</li>
	<li>Incubate at 37 &deg;C for 1 to 20 min, depending on the nuclear factor of interest. For NF-&kappa;B usually 15 min, and for Elk-1 usually 5 min. 
	Note: Incubating the cells at 37 &deg;C induces receptor crosslinking, which cannot take place at 4 &deg;C.</li>
	<li>Add 1 ml cold PBS and centrifuge 3 min at 1,743 x g in microcentrifuge.</li>
	<li>Remove supernatant</li>
	<li>Freeze PMN immediately in dry-ice/ethanol bath and keep them there for 10 min.</li>
</ol>
3. Isolation and Fixation of Nuclei
<ol>
	<li>Resuspend frozen PMN pellet in 100 &mu;l cold (4 &deg;C) hypotonic buffer (10 mM HEPES, 10 mM KCl, 1.5 mM MgCl2, and 1 mM freshly-added DL-dithiothreitol [DTT]; pH = 7.9). It is recommended to take the tubes out of the dry-ice/ethanol bath one by one, and to wipe clean the bottom of the tube before adding the hypotonic buffer.</li>
	<li>Place on ice, and check for nuclei integrity by staining an aliquot of the nuclei suspension with trypan blue. Nuclei look round and blue. Intact PMN do not get stained, and cell debris appears as blue particles of irregular shape. 
	Note: If nuclei suspension contains many intact cells or debris, it is better to discard the preparation and repeat the procedure with another sample.</li>
	<li>Centrifuge nuclei at 775 x g (3,000 rpm) in microcentrifuge for 10 min inside a cold room. At this point nuclei are very fragile and extra care should be taken in keeping the samples cold and not centrifuging at excessive forces.</li>
	<li>Remove supernatant by very careful pipetting.</li>
	<li>Add 100 &mu;l of cold 4% paraformaldehyde in PBS to fix nuclei. 
	Note: The pellet is very loose and adding the buffer is enough to resuspend the nuclei. Pipetting up and down should be avoided.</li>
	<li>Incubate on ice for 20 min.</li>
	<li>Immunolabel nuclei for flow cytometry or keep them for up to 24 hr at 4 &deg;C.</li>
</ol>
4. Nuclei Immunolabeling for Flow Cytometry Analysis
<ol>
	<li>Centrifuge nuclei at 1,743 x g (4,500 rpm) in microcentrifuge for 1 min, and remove supernatant by very gentle pipetting.</li>
	<li>Add 100 &mu;l of cold (4 &deg;C) 0.1% Triton X-100, 4% paraformaldehyde in PBS to permeabilize nuclei. Incubate in ice for 10 min.</li>
	<li>Centrifuge permeabilized nuclei at 1,743 x g in microcentrifuge and carefully remove the supernatant. At this point nuclei pellets do not attach well at the bottom of the tube. It is recommended to centrifuge again if the pellet gets loose.</li>
	<li>Resuspend nuclei in 500 &mu;l of cold 4% fetal bovine serum (FBS) in PBS to block nonspecific binding sites, and incubate on ice for 20 min. Centrifuge nuclei at 1,743 x g for 3 min in microcentrifuge and carefully remove the supernatant.</li>
	<li>Resuspend nuclei in 100 &mu;l of cold PBS containing 4% FBS and 2.5 &mu;g/ml of the mAb against the nuclear factor of interest. Incubate on ice for 20 min. 
	Note: Usual negative controls should include anti-nuclear factor antibody only, and FITC-labeled secondary antibody only.</li>
	<li>Wash twice with 500 &mu;l of cold PBS with 4% FBS and centrifuging at 1743 x g for 3 min.</li>
	<li>Remove the supernatant very carefully, resuspend nuclei in 100 &mu;l of cold PBS containing 4% FBS and 10 &mu;g/ml of the corresponding FITC-labeled secondary antibody, and incubate on ice for 20 min.</li>
	<li>Wash nuclei twice with 500 &mu;l of cold PBS with 4% FBS as in previous step.</li>
	<li>Resuspend nuclei in 400 &mu;l of cold 4% paraformaldehyde in PBS. 
	Note: Nuclei are placed in paraformaldehyde to allow the sample to be stored for several days without contamination problems that can occur in the presence of serum.</li>
	<li>Analyze immediately by flow cytometry or store in the dark at 4 &deg;C for up to three days.</li>
</ol>
5. Flow Cytometry Analysis
<ol>
	<li>Analyze immunolabeled nuclei in a flow cytometer such a FACScan (Becton Dickinson; Franklin Lakes, NJ) or similar apparatus.</li>
	<li>Adjust acquisition settings to: FSC at log-scale at 10-1, SSC at log-scale at 196, and gate nuclei in a dot-plot.</li>
	<li>Acquire ten thousand nuclei per sample.</li>
	<li>Analyze fluorescence of FITC-stained nuclei through the FL-1 channel (506 nm) set at log-scale at 400.</li>
</ol>

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A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Regulating+neutrophil+apoptosis:+new+players+enter+the+game.">Regulating neutrophil apoptosis: new players enter the game.</a> Trends Immunol. 32, 117-124 (2011).</li><li>Green, D. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Death+and+NF-&#954;B+in+T+cell+activation:+life+at+the+edge.">Death and NF-&#954;B in T cell activation: life at the edge.</a> Mol. Cell. 11, 551-552 (2003).</li><li>Papa, S., Zazzeroni, F., Pham, C. G., Bubici, C., Franzoso, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Linking+JNK+signaling+to+NF-&#954;B:+a+key+to+survival.">Linking JNK signaling to NF-&#954;B: a key to survival.</a> J. 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Cancer. 39, 1468-1477 (2003).</li><li>Choi, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inhibition+of+NF-&#954;B+by+a+TAT-NEMO-binding+domain+peptide+accelerates+constitutive+apoptosis+and+abrogates+LPS-delayed+neutrophil+apoptosis.">Inhibition of NF-&#954;B by a TAT-NEMO-binding domain peptide accelerates constitutive apoptosis and abrogates LPS-delayed neutrophil apoptosis.</a> Blood. 102, 2259-2267 (2003).</li><li>Wang, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Inhibition+of+neutrophil+apoptosis+by+type+1+IFN+depends+on+cross-talk+between+phosphoinositol+3-kinase,+protein+kinase+C-d,+and+NF-&#954;B+signaling+pathways.">Inhibition of neutrophil apoptosis by type 1 IFN depends on cross-talk between phosphoinositol 3-kinase, protein kinase C-d, and NF-&#954;B signaling pathways.</a> J. Immunol. 171, 1035-1041 (2003).</li><li>Schnoor, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Efficient+non-viral+transfection+of+THP-1+cells.">Efficient non-viral transfection of THP-1 cells.</a> J. Immunol. Meth. 344, 109-115 (2009).</li><li>Garcia-Garcia, E., Rosales, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nuclear+factor+activation+by+Fc&#947;R+in+human+peripheral+blood+neutrophils+detected+by+a+novel+flow+cytometry-based+method.">Nuclear factor activation by Fc&#947;R in human peripheral blood neutrophils detected by a novel flow cytometry-based method.</a> J. Immunol. Meth. 320, 104-118 (2007).</li><li>Garcia-Garcia, E., Nieto-Castaneda, G., Ruiz-Saldana, M., Mora, N., Rosales, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fc&#947;RIIA+and+Fc&#947;RIIIB+mediate+nuclear+factor+activation+through+separate+signaling+pathways+in+human+neuthophils.">Fc&#947;RIIA and Fc&#947;RIIIB mediate nuclear factor activation through separate signaling pathways in human neuthophils.</a> J. Immunol. 182, 4547-4556 (2009).</li></ol>

The authors declare that they have no competing financial interests.

The purification method described here allows the isolation of unstimulated neutrophils (PMN) with purity greater than 95% (assessed by microscopic observation), in a short time. Sometimes neutrophils can be contaminated by erythrocytes if the latter are not lysed completely. This does not usually affect the technique, since erythrocytes and PMN can easily be distinguished as distinct cell populations by flow cytometry. Isolated PMN can then be stimulated by crosslinking particular receptors with specific monoclon...

Neutrophils are the most abundant leukocytes in peripheral blood 1. During inflammation and infection neutrophils are the first cells to appear at the affected site where they act as the first line of defense 2. Neutrophils possess several antimicrobial mechanisms 3 including phagocytosis, production of reactive oxygen species, release of lytic enzymes by degranulation, and production of proinflammatory cytokines 4,5. Neutrophils are short-lived cells that get rapidly activated through signaling from various cell surface receptors. Although neutrophils have been considered terminal cells due to their short life and because they undergo apoptosis unless activated during the inflammatory process 6, it is now clear that they can also modify their phenotype by changing the level of transcription of particular genes. The production of cytokines 5 and the inhibition of apoptosis 7,8 are two important activation-dependent cell functions regulated at the level of transcription in neutrophils. Nuclear factor &kappa;B (NF-&kappa;B) participates in the transcriptional control of cytokine production 4 and in the regulation of cell survival and apoptosis 9-11 in various cell types.
The signaling pathways that lead to nuclear factor activation are usually studied by reporter gene assays or by electrophoretic mobility shift assays (EMSA). However, because neutrophils are short-lived cells, the study of transcriptionally regulated responses in these cells cannot be performed with reporter gene assays, since there are no efficient techniques for neutrophil transfection. EMSA assays have been used in neutrophils to explore nuclear factor activation 12,13; however, this methodology is complicated and expensive because it involves the use of radioactive material. Nucleofection is another technique that has been used successfully to transfect monocytes 14. Thus, at least in theory, nuclear factor activation could be detected in neutrophils by transfection (despite low efficiency). However, this technique would be more expensive, time-consuming and probably less quantitative. Microscopic analysis of immunostained cells could also be used to detect nuclear factors in the nucleus. Indeed, we have detected NF-&kappa;B translocation into the nucleus this way 15. Unfortunately, this technique is also time-consuming, less quantitative, and subject to the observer's bias.
Here, we present a simple and efficient method that allows detection and quantification of nuclear factors in isolated and immunolabeled nuclei by flow cytometry. We describe techniques to isolate neutrophils from human peripheral blood, stimulate these cells via integrins or Fc receptors with anti-receptor antibodies, isolate and immunolabel nuclei, and analyze nuclei by flow cytometry (Figure 1). The method has been successfully used to detect NF-&kappa;B 15 and Elk-1 16 nuclear factors in neutrophil nuclei. The sensitivity of this method allows detection of small changes in nuclear factor levels in the nucleus. This method can also be used to analyze the level of transcription factors in nuclei from other cell types.

<table border="1">
<tbody>
 <tr>
 <td></td>
 <td></td>
 <td></td>
 <td>REAGENTS</td>
 </tr>
 <tr>
 <td >Heparin </td>
 <td >PiSA (Mexico)</td>
 <td></td>
 <td></td>
 </tr>
 <tr>
 <td >Dextran T500</td>
 <td >Pharmacosmos A/S (Holbaek, Denmark) </td>
 <td>T1-Dextran T500</td>
 <td></td>
 </tr>
 <tr>
 <td >Ficoll-Paque</td>
 <td >Pharmacia</td>
 <td>17-0320-01 </td>
 <td></td>
 </tr>
 <tr>
 <td >Sodium chloride </td>
 <td >Sigma</td>
 <td>S7653 </td>
 <td></td>
 </tr>
 <tr>
 <td >Sodium phosphate monobasic</td>
 <td >Sigma</td>
 <td>S9638</td>
 <td></td>
 </tr>
 <tr>
 <td >Sodium phosphate dibasic</td>
 <td >Sigma</td>
 <td>S9390</td>
 <td></td>
 </tr>
 <tr>
 <td >Bovine serum albumin (BSA)</td>
 <td >Sigma</td>
 <td>A2153</td>
 <td>Cohn Fraction V</td>
 </tr>
 <tr>
 <td >HEPES</td>
 <td >Sigma</td>
 <td>H3375 </td>
 <td></td>
 </tr>
 <tr>
 <td >Potassium chloride</td>
 <td >Sigma</td>
 <td>P9541 </td>
 <td></td>
 </tr>
 <tr>
 <td >Magnesium chloride anhydrous </td>
 <td >Sigma</td>
 <td>M8266 </td>
 <td></td>
 </tr>
 <tr>
 <td >DL-dithiothreitol (DTT) </td>
 <td >Sigma</td>
 <td>D9163</td>
 <td></td>
 </tr>
 <tr>
 <td >Trypan Blue (0.4 % solution)</td>
 <td >Sigma</td>
 <td>T8154</td>
 <td></td>
 </tr>
 <tr>
 <td >Paraformaldehyde</td>
 <td >Sigma</td>
 <td>P6148 </td>
 <td></td>
 </tr>
 <tr>
 <td >Triton X-100 </td>
 <td >Sigma</td>
 <td>X100</td>
 <td></td>
 </tr>
 <tr>
 <td >Fetal bovine serum (FBS)</td>
 <td >GIBCO</td>
 <td>10437-028</td>
 <td></td>
 </tr>
 <tr>
 <td >Monoclonal antibody IV.3</td>
 <td >Medarex (Annandale, NJ) </td>
 <td>025-1 </td>
 <td>Human-specific anti-FcRII (CD32) </td>
 </tr>
 <tr>
 <td >Monoclonal antibody 3G8</td>
 <td >Medarex (Annandale, NJ) </td>
 <td>028-2 </td>
 <td>Human-specific anti-FcRIII (CD16) </td>
 </tr>
 <tr>
 <td >Monoclonal antibody TS2/16</td>
 <td >Dana Farber Cancer Research Institute (Boston, MA) </td>
 <td>Donated by Dr. Martin Hemler </td>
 <td>Human-specific anti-&beta;1 integrin (CD29)</td>
 </tr>
 <tr>
 <td >Monoclonal antibody IB4</td>
 <td >University of California, San Francisco </td>
 <td>Donated by Dr. Eric J. Brown </td>
 <td>Human-specific anti-&beta;2 integrin (CD18)</td>
 </tr>
 <tr>
 <td >F(ab')2 goat anti-mouse IgG </td>
 <td >Cappel (Aurora, OH)</td>
 <td>55468</td>
 <td></td>
 </tr>
 <tr>
 <td>FITC-conjugated F(ab')2 goat anti-mouse IgG</td>
 <td >Cappel (Aurora, OH)</td>
 <td>55522</td>
 <td></td>
 </tr>
 <tr>
 <td>FITC-conjugated F(ab')2 goat anti-rabbit IgG</td>
 <td >Cappel (Aurora, OH)</td>
 <td>55665</td>
 <td></td>
 </tr>
 <tr>
 <td>Anti-NF-&kappa;B p50</td>
 <td >Santa Cruz Biotechnology (Santa Cruz, CA)</td>
 <td>sc-114</td>
 <td>Rabbit polyclonal antibody</td>
 </tr>
 <tr>
 <td>Anti-NF-&kappa;B p65</td>
 <td >Santa Cruz Biotechnology (Santa Cruz, CA)</td>
 <td>sc-109</td>
 <td>Rabbit polyclonal antibody</td>
 </tr>
 <tr>
 <td></td>
 <td></td>
 <td></td>
 <td>EQUIPMENT</td>
 </tr>
 <tr>
 <td>15-ml centrifuge tube</td>
 <td >Corning</td>
 <td>430791</td>
 <td></td>
 </tr>
 <tr>
 <td>50-ml centrifuge tube</td>
 <td >Corning</td>
 <td>430291</td>
 <td></td>
 </tr>
 <tr>
 <td>Centrifuge, Sorvall Tabletop</td>
 <td >Dupont Instruments</td>
 <td>RT 6000D</td>
 <td></td>
 </tr>
 <tr>
 <td>pH-meter</td>
 <td >Corning</td>
 <td>340</td>
 <td></td>
 </tr>
 <tr>
 <td>Pipetman pipette P-20</td>
 <td >Gilson </td>
 <td>F123600</td>
 <td></td>
 </tr>
 <tr>
 <td>Pipetman pipette P-200</td>
 <td >Gilson </td>
 <td>F123601</td>
 <td></td>
 </tr>
 <tr>
 <td>Pipetman pipette P-1000</td>
 <td >Gilson </td>
 <td>F123602</td>
 <td></td>
 </tr>
 <tr>
 <td>Hemocytometer</td>
 <td >Fisher Scientific</td>
 <td>0267110</td>
 <td></td>
 </tr>
 <tr>
 <td>Microscope</td>
 <td >Nikon </td>
 <td>Eclipse E600</td>
 <td></td>
 </tr>
 <tr>
 <td>Inverted microscope</td>
 <td >Nikon </td>
 <td>TMS</td>
 <td></td>
 </tr>
 <tr>
 <td>Water Bath Incubator</td>
 <td >Fisher Scientific </td>
 <td>2IS-M</td>
 <td></td>
 </tr>
 <tr>
 <td>Microcentrifuge</td>
 <td >Eppendorf</td>
 <td>5414C</td>
 <td></td>
 </tr>
 <tr>
 <td>Microcentrifuge</td>
 <td >Eppendorf</td>
 <td>5418</td>
 <td></td>
 </tr>
 <tr>
 <td>Flow Cytometer</td>
 <td >Becton Dickinson (Franklin Lakes, NJ) </td>
 <td>FACScalibur </td>
 <td></td>
 </tr>
 </tbody>
</table>

a simple and efficient method to detect nuclear factor activation in human neutrophils by flow cytometry

Neutrophils are the most abundant leukocytes in peripheral blood. These cells are the first to appear at sites of inflammation and infection, thus becoming the first line of defense against invading microorganisms. Neutrophils possess important antimicrobial functions such as phagocytosis, release of lytic enzymes, and production of reactive oxygen species. In addition to these important defense functions, neutrophils perform other tasks in response to infection such as production of proinflammatory cytokines and inhibition of apoptosis. Cytokines recruit other leukocytes that help clear the infection, and inhibition of apoptosis allows the neutrophil to live longer at the site of infection. These functions are regulated at the level of transcription. However, because neutrophils are short-lived cells, the study of transcriptionally regulated responses in these cells cannot be performed with conventional reporter gene methods since there are no efficient techniques for neutrophil transfection. Here, we present a simple and efficient method that allows detection and quantification of nuclear factors in isolated and immunolabeled nuclei by flow cytometry. We describe techniques to isolate pure neutrophils from human peripheral blood, stimulate these cells with anti-receptor antibodies, isolate and immunolabel nuclei, and analyze nuclei by flow cytometry. The method has been successfully used to detect NF-&kappa;B and Elk-1 nuclear factors in nuclei from neutrophils and other cell types. Thus, this method represents an option for analyzing activation of transcription factors in isolated nuclei from a variety of cell types.

The purification method described here usually provides unstimulated neutrophils (PMN) with purity greater than 95% (Figure 1A). Isolated PMN can then be stimulated by crosslinking particular receptors with specific monoclonal antibodies. We have stimulated PMN through Fc receptors and integrins (Figure 1B). Once stimulated, PMN are lysed and nuclei are isolated with high yields. Nuclei are then immunolabeled for a particular nuclear factor, such as the nuclear factor &kappa;B (NF-&...

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A Simple and Efficient Method to Detect Nuclear Factor Activation in Human Neutrophils by Flow Cytometry

Neutrophils are the most abundant leukocytes in blood. Neutrophils possess transcriptionally regulated functions such as production of proinflammatory cytokines and inhibition of apoptosis. These functions can be studied with the method presented here, which allows detection and quantification of nuclear factors by flow cytometry in isolated nuclei

Neutrophils  are the most abundant leukocytes in peripheral blood. These cells are the first  to appear at sites of inflammation and infection, thus ...

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17.7K Views.  University of Alberta. Neutrophils are the most abundant leukocytes in blood. Neutrophils possess transcriptionally regulated functions such as production of proinflammatory cytokines and inhibition of apoptosis. These functions can be studied with the method presented here, which allows detection and quantification of nuclear factors by flow cytometry in isolated nuclei