bm16 Search Results


cd294 (crth2) antibody, anti-human  (Miltenyi Biotec)
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Miltenyi Biotec cd294 (crth2) antibody, anti-human
Cd294 (Crth2) Antibody, Anti Human, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd294 (crth2) antibody, anti-human/product/Miltenyi Biotec
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3163003b rrid ab 2810253  (fluidigm)
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fluidigm 3163003b rrid ab 2810253
3163003b Rrid Ab 2810253, supplied by fluidigm, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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phycoerythrin (pe)-cf594–conjugated anti-crth2  (Becton Dickinson)
90
Becton Dickinson phycoerythrin (pe)-cf594–conjugated anti-crth2
Phycoerythrin (Pe) Cf594–Conjugated Anti Crth2, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cd294 alexa 647 (crth2 ab  (Becton Dickinson)
90
Becton Dickinson cd294 alexa 647 (crth2 ab
Flow-cytometric analysis of T cell proliferation and Th cell polarization. CFSE-labeled CD4 + T cells from HDM-allergic or HDM-nonallergic individuals were cultured with Der p or glycerin as described in . T cell division was analyzed by flow cytometry and illustrated as a CFSE division profile (a). Dead cells were excluded based on their light scattering properties. Nondividing CD4 + T cells in the absence of allergen are shown as dark grey histograms. CD4 + T cells that have divided in response to Der p are shown in light grey histograms, based on CFSE dilution peaks. One representative experiment of three is illustrated. In vitro polarization of human Th1 and Th2 precursors following 11 days of culture with glycerin or Der p was determined by flow cytometry using Alexa-conjugated Abs for human CXCR3 (b) or <t>CRTH2</t> (c), respectively. Data are expressed as geometric mean (±SEM) fluorescence intensity (MFI). P values are indicated. HDMA = house dust mite-allergic donors. Th2/Th1 ratio of CD4 + T cells from HDM-allergic donors following 11 days of culture with glycerin or Der p (d), n = 6; Th2/Th1 ratio of Der p-stimulated CD4 + T cells from nonallergic and HDM-allergic individuals (e), n = 6 for controls; n = 10 for HDMA.
Cd294 Alexa 647 (Crth2 Ab, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cd294 alexa 647 (crth2 ab/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
cd294 alexa 647 (crth2 ab - by Bioz Stars, 2026-03
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anti-human crth2 in pe and percp 5.5 (bm16)  (Sony)
90
Sony anti-human crth2 in pe and percp 5.5 (bm16)
Flow-cytometric analysis of T cell proliferation and Th cell polarization. CFSE-labeled CD4 + T cells from HDM-allergic or HDM-nonallergic individuals were cultured with Der p or glycerin as described in . T cell division was analyzed by flow cytometry and illustrated as a CFSE division profile (a). Dead cells were excluded based on their light scattering properties. Nondividing CD4 + T cells in the absence of allergen are shown as dark grey histograms. CD4 + T cells that have divided in response to Der p are shown in light grey histograms, based on CFSE dilution peaks. One representative experiment of three is illustrated. In vitro polarization of human Th1 and Th2 precursors following 11 days of culture with glycerin or Der p was determined by flow cytometry using Alexa-conjugated Abs for human CXCR3 (b) or <t>CRTH2</t> (c), respectively. Data are expressed as geometric mean (±SEM) fluorescence intensity (MFI). P values are indicated. HDMA = house dust mite-allergic donors. Th2/Th1 ratio of CD4 + T cells from HDM-allergic donors following 11 days of culture with glycerin or Der p (d), n = 6; Th2/Th1 ratio of Der p-stimulated CD4 + T cells from nonallergic and HDM-allergic individuals (e), n = 6 for controls; n = 10 for HDMA.
Anti Human Crth2 In Pe And Percp 5.5 (Bm16), supplied by Sony, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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monitor bm 16  (Beurer GmbH)
90
Beurer GmbH monitor bm 16
Flow-cytometric analysis of T cell proliferation and Th cell polarization. CFSE-labeled CD4 + T cells from HDM-allergic or HDM-nonallergic individuals were cultured with Der p or glycerin as described in . T cell division was analyzed by flow cytometry and illustrated as a CFSE division profile (a). Dead cells were excluded based on their light scattering properties. Nondividing CD4 + T cells in the absence of allergen are shown as dark grey histograms. CD4 + T cells that have divided in response to Der p are shown in light grey histograms, based on CFSE dilution peaks. One representative experiment of three is illustrated. In vitro polarization of human Th1 and Th2 precursors following 11 days of culture with glycerin or Der p was determined by flow cytometry using Alexa-conjugated Abs for human CXCR3 (b) or <t>CRTH2</t> (c), respectively. Data are expressed as geometric mean (±SEM) fluorescence intensity (MFI). P values are indicated. HDMA = house dust mite-allergic donors. Th2/Th1 ratio of CD4 + T cells from HDM-allergic donors following 11 days of culture with glycerin or Der p (d), n = 6; Th2/Th1 ratio of Der p-stimulated CD4 + T cells from nonallergic and HDM-allergic individuals (e), n = 6 for controls; n = 10 for HDMA.
Monitor Bm 16, supplied by Beurer GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/monitor bm 16/product/Beurer GmbH
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monitor bm 16 - by Bioz Stars, 2026-03
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bm 16.2115  (Boehringer Mannheim)
90
Boehringer Mannheim bm 16.2115
Flow-cytometric analysis of T cell proliferation and Th cell polarization. CFSE-labeled CD4 + T cells from HDM-allergic or HDM-nonallergic individuals were cultured with Der p or glycerin as described in . T cell division was analyzed by flow cytometry and illustrated as a CFSE division profile (a). Dead cells were excluded based on their light scattering properties. Nondividing CD4 + T cells in the absence of allergen are shown as dark grey histograms. CD4 + T cells that have divided in response to Der p are shown in light grey histograms, based on CFSE dilution peaks. One representative experiment of three is illustrated. In vitro polarization of human Th1 and Th2 precursors following 11 days of culture with glycerin or Der p was determined by flow cytometry using Alexa-conjugated Abs for human CXCR3 (b) or <t>CRTH2</t> (c), respectively. Data are expressed as geometric mean (±SEM) fluorescence intensity (MFI). P values are indicated. HDMA = house dust mite-allergic donors. Th2/Th1 ratio of CD4 + T cells from HDM-allergic donors following 11 days of culture with glycerin or Der p (d), n = 6; Th2/Th1 ratio of Der p-stimulated CD4 + T cells from nonallergic and HDM-allergic individuals (e), n = 6 for controls; n = 10 for HDMA.
Bm 16.2115, supplied by Boehringer Mannheim, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Flow-cytometric analysis of T cell proliferation and Th cell polarization. CFSE-labeled CD4 + T cells from HDM-allergic or HDM-nonallergic individuals were cultured with Der p or glycerin as described in . T cell division was analyzed by flow cytometry and illustrated as a CFSE division profile (a). Dead cells were excluded based on their light scattering properties. Nondividing CD4 + T cells in the absence of allergen are shown as dark grey histograms. CD4 + T cells that have divided in response to Der p are shown in light grey histograms, based on CFSE dilution peaks. One representative experiment of three is illustrated. In vitro polarization of human Th1 and Th2 precursors following 11 days of culture with glycerin or Der p was determined by flow cytometry using Alexa-conjugated Abs for human CXCR3 (b) or CRTH2 (c), respectively. Data are expressed as geometric mean (±SEM) fluorescence intensity (MFI). P values are indicated. HDMA = house dust mite-allergic donors. Th2/Th1 ratio of CD4 + T cells from HDM-allergic donors following 11 days of culture with glycerin or Der p (d), n = 6; Th2/Th1 ratio of Der p-stimulated CD4 + T cells from nonallergic and HDM-allergic individuals (e), n = 6 for controls; n = 10 for HDMA.

Journal: Journal of Immunology Research

Article Title: Enhanced Cysteinyl-Leukotriene Type 1 Receptor Expression in T Cells from House Dust Mite-Allergic Individuals following Stimulation with Der p

doi: 10.1155/2015/384780

Figure Lengend Snippet: Flow-cytometric analysis of T cell proliferation and Th cell polarization. CFSE-labeled CD4 + T cells from HDM-allergic or HDM-nonallergic individuals were cultured with Der p or glycerin as described in . T cell division was analyzed by flow cytometry and illustrated as a CFSE division profile (a). Dead cells were excluded based on their light scattering properties. Nondividing CD4 + T cells in the absence of allergen are shown as dark grey histograms. CD4 + T cells that have divided in response to Der p are shown in light grey histograms, based on CFSE dilution peaks. One representative experiment of three is illustrated. In vitro polarization of human Th1 and Th2 precursors following 11 days of culture with glycerin or Der p was determined by flow cytometry using Alexa-conjugated Abs for human CXCR3 (b) or CRTH2 (c), respectively. Data are expressed as geometric mean (±SEM) fluorescence intensity (MFI). P values are indicated. HDMA = house dust mite-allergic donors. Th2/Th1 ratio of CD4 + T cells from HDM-allergic donors following 11 days of culture with glycerin or Der p (d), n = 6; Th2/Th1 ratio of Der p-stimulated CD4 + T cells from nonallergic and HDM-allergic individuals (e), n = 6 for controls; n = 10 for HDMA.

Article Snippet: On day 11, cells were harvested and incubated for 30 minutes at 4°C with fluorochrome-conjugated monoclonal antibodies: CD184 PE (CXCR4 Ab), CD183 Alexa 488 (CXCR3 Ab), and CD294 Alexa 647 (CRTH2 Ab) (BD Pharmingen, San Diego, CA, USA) antibodies known to recognize Th cell surface markers associated with Th0, Th1, and Th2, respectively [ , ].

Techniques: Labeling, Cell Culture, Flow Cytometry, In Vitro, Fluorescence