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![Flow Cytometry: phycoerythrin Antibody (PE-DLF) [NBP2-00146] - Analysis using the Biotin conjugate of NBP2-00146. Staining of C57BL/6 splenocytes with Anti Human/Mouse CD45R (B220) PE and 0.06 ug of Mouse IgG1 kappa Isotype Control Biotin (left) or 0.06 ug of Anti-Phycoerythrin Biotin (right) followed by Streptavidin APC.](http://images.novusbio.com/fullsize/phycoerythrin-Antibody-PE-DLF-Flow-Cytometry-NBP2-00146-img0003.jpg "Flow Cytometry: phycoerythrin Antibody (PE-DLF) [NBP2-00146] - Analysis using the Biotin conjugate of NBP2-00146. Staining of C57BL/6 splenocytes with Anti Human/Mouse CD45R (B220) PE and 0.06 ug of Mouse IgG1 kappa Isotype Control Biotin (left) or 0.06 ug of Anti-Phycoerythrin Biotin (right) followed by Streptavidin APC.")
![Flow Cytometry: phycoerythrin Antibody (PE-DLF) [NBP2-00146] - Staining of normal human peripheral blood cells with Rat Anti-Human/Mouse CD44 PE , followed by 0.125 ug of Mouse IgG1 K Isotype Control Purified (left) or 0.125 ug of Anti-Phycoerythrin Purified (right), followed by detection with Anti-Mouse IgG FITC. Total viable cells were used for analysis.](http://images.novusbio.com/fullsize/phycoerythrin-Antibody-PE-DLF-Flow-Cytometry-NBP2-00146-img0001.jpg)
![Flow Cytometry: phycoerythrin Antibody (PE-DLF) [Biotin] [NBP2-00145] - Staining of C57BL/6 splenocytes with Anti Human/Mouse CD45R (B220) PE and 0.06 ug of Mouse IgG1 kappa Isotype Control Biotin (left) or 0.06 ug of Anti-Phycoerythrin Biotin (right) followed by Streptavidin APC . Total viable cells were used for analysis.](http://images.novusbio.com/fullsize/phycoerythrin-Antibody-PE-DLF-Biotin-Flow-Cytometry-NBP2-00145-img0001.jpg "Flow Cytometry: phycoerythrin Antibody (PE-DLF) [Biotin] [NBP2-00145] - Staining of C57BL/6 splenocytes with Anti Human/Mouse CD45R (B220) PE and 0.06 ug of Mouse IgG1 kappa Isotype Control Biotin (left) or 0.06 ug of Anti-Phycoerythrin Biotin (right) followed by Streptavidin APC . Total viable cells were used for analysis.")
![Flow Cytometry: Lightning-Link B-Phycoerythrin Antibody Labeling Kit [716-0010] - Mouse anti-human CD3 was conjugated with B Phycoerythrin using a Lightning-Link kit. The conjugated antibody was then used to stain human peripheral blood lymphocytes, followed by analysis with flow cytometry. (Blue line - negative control; red line - positive staining).](http://images.novusbio.com/fullsize/Lightning-Link-B-Phycoerythrin-Antibody-Labeling-Kit-Flow-Cytometry-716-0010-img0001.jpg "Flow Cytometry: Lightning-Link B-Phycoerythrin Antibody Labeling Kit [716-0010] - Mouse anti-human CD3 was conjugated with B Phycoerythrin using a Lightning-Link kit. The conjugated antibody was then used to stain human peripheral blood lymphocytes, followed by analysis with flow cytometry. (Blue line - negative control; red line - positive staining).")
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0010] - Direct labeling with Lightning Link CD45RC-PE](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0010-img0006.jpg "Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0010] - Direct labeling with Lightning Link CD45RC-PE")
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0010] - Indirect labeling with CD45RC supernatant](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0010-img0004.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0010] - Indirect labeling with purified CD45RC antibody](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0010-img0005.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0030] - Direct labeling with Lightning Link CD45RC-PE](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0030-img0006.jpg "Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0030] - Direct labeling with Lightning Link CD45RC-PE")
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0030] - Indirect labeling with CD45RC supernatant](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0030-img0004.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0030] - Indirect labeling with purified CD45RC antibody](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0030-img0005.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0015] - Direct labeling with Lightning Link CD45RC-PE](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0015-img0006.jpg "Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0015] - Direct labeling with Lightning Link CD45RC-PE")
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0015] - Indirect labeling with CD45RC supernatant](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0015-img0004.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0015] - Indirect labeling with purified CD45RC antibody](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0015-img0005.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0005] - Direct labeling with Lightning Link CD45RC-PE](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0005-img0006.jpg "Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0005] - Direct labeling with Lightning Link CD45RC-PE")
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0005] - Indirect labeling with CD45RC supernatant](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0005-img0004.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0005] - Indirect labeling with purified CD45RC antibody](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0005-img0005.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0003] - Mouse anti-human CD8 was conjugated with R Phycoerythrin using Lightning-Link kit. The conjugated antibody was then used to stain human peripheral blood lymphocytes, followed by analysis with flow cytometry. (Blue line - negative control; red line - positive staining).](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0003-img0003.jpg "Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0003] - Mouse anti-human CD8 was conjugated with R Phycoerythrin using Lightning-Link kit. The conjugated antibody was then used to stain human peripheral blood lymphocytes, followed by analysis with flow cytometry. (Blue line - negative control; red line - positive staining).")
![Lightning-Link R-PE Antibody Labeling Kit [703-0003]](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-703-0003-img0001.jpg)
![Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0004] - ndirect labeling with CD45RC supernatant (left). Indirect labeling with CD45RC purified antibody (middle). Direct labeling with Lightning-Link CD45RC-PE Purified antibody (left).](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-Flow-Cytometry-703-0004-img0001.jpg "Flow Cytometry: Lightning-Link R-PE Antibody Labeling Kit [703-0004] - ndirect labeling with CD45RC supernatant (left). Indirect labeling with CD45RC purified antibody (middle). Direct labeling with Lightning-Link CD45RC-PE Purified antibody (left).")
![Lightning-Link R-PE Antibody Labeling Kit [703-0004] - Mouse anti-human CD8 was conjugated with R-Phycoerythrin using an Expedeon Lightning-Link kit. The conjugated antibody was then used to stain human peripheral blood lymphocytes, followed by analysis with flow cytometry. (Blue line - negative control; red line - positive staining).](http://images.novusbio.com/fullsize/Lightning-Link-R-PE-Antibody-Labeling-Kit-703-0004-img0002.jpg)
![Soluble factors increase the numbers of Hes3+ cells in the adult rat hippocampus.(a) Treatment with the soluble factors induced a powerful increase in the number of Sox2+ cells in the hilus [Quantifications are from images taken from the tip of the hilus to approximately 1,300 micrometers towards the CA3 region – representative images are shown. Staining for the young neuron marker doublecortin (DCX) helps to visualize the subgranular zone]. (b) The same treatment also induced an increase in the numbers of Hes3+ cells in the hilus. (c) Sox2+ cells inside the hilus co-expressed Hes3; in contrast, Sox2+ cells in the subgranular zone did not co-express Hes3. (d,e) Quantification graphs of the increases in Sox2+ and Hes3+ cell numbers in the hilus (p0.05; *, p0.05, #, p C) in exon 2 of the SMPD1 gene. D) Flow cytometry analysis of pluripotency protein markers: NANOG and TRA-1–60. E) RT-PCR verification for the clearance of the Sendai virus from reprogrammed cells. Sendai virus vector transduced fibroblasts were used as a positive control. F) Pathological analysis of teratoma from TRNDi009-C iPSC, showing a normal ectodermal, mesodermal, and endodermal differentiation. Image collected and cropped by CiteAb from the following publication (//pubmed.ncbi.nlm.nih.gov/31132580), licensed under a CC-BY license. Not internally tested by R&D Systems.](http://images.novusbio.com/fullsize/mab2018_human-mouse-rat-sox2-mab-clone-245610-22820241723619.jpg)
