dc assay kit Search Results


pan dc enrichment kit  (Miltenyi Biotec)
95
Miltenyi Biotec pan dc enrichment kit
Pan Dc Enrichment Kit, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/10__21769_slash_bioprotoc__4881-85-0-4?v=Miltenyi+Biotec
Average 95 stars, based on 1 article reviews
pan dc enrichment kit - by Bioz Stars, 2026-07
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d mannitol  (Chem Impex International)
95
Chem Impex International d mannitol
D Mannitol, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/pmc12590514-225-120-122?v=Chem+Impex+International
Average 95 stars, based on 1 article reviews
d mannitol - by Bioz Stars, 2026-07
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protein concentration  (Bio-Rad)
97
Bio-Rad protein concentration
Protein Concentration, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/pmc13023512-83-2-13?v=Bio-Rad
Average 97 stars, based on 1 article reviews
protein concentration - by Bioz Stars, 2026-07
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rcdc assay kit  (Bio-Rad)
96
Bio-Rad rcdc assay kit
Rcdc Assay Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
rcdc assay kit - by Bioz Stars, 2026-07
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dc protein assay kit  (Bio-Rad)
96
Bio-Rad dc protein assay kit
Dc Protein Assay Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
dc protein assay kit - by Bioz Stars, 2026-07
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biorad rd dc kit  (Bio-Rad)
94
Bio-Rad biorad rd dc kit
Biorad Rd Dc Kit, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/clair_eva_s_t__2021__targeted_edv_tm_nanocells_carrying_small_interfering_rna_sirna_molecules_to_overcome_drug_resistance_in_non-881-6-9?v=Bio-Rad
Average 94 stars, based on 1 article reviews
biorad rd dc kit - by Bioz Stars, 2026-07
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human monocyte  (R&D Systems)
93
R&D Systems human monocyte
Human Monocyte, supplied by R&D Systems, 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/product/dc+assay+kit/pmc11971868-80-25-31?v=R%26D+Systems
Average 93 stars, based on 1 article reviews
human monocyte - by Bioz Stars, 2026-07
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dendritic cell differentiation kit  (R&D Systems)
94
R&D Systems dendritic cell differentiation kit
Dendritic Cell Differentiation Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/pmc10562189-193-11-15?v=R%26D+Systems
Average 94 stars, based on 1 article reviews
dendritic cell differentiation kit - by Bioz Stars, 2026-07
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mo dc differentiation inspector antibody cocktail  (Miltenyi Biotec)
97
Miltenyi Biotec mo dc differentiation inspector antibody cocktail
FIGURE 2 | Expression of ANKRD55 and neighboring genes in immature moDC. (A–D) Monocytes were cultivated for 6 days in IL-4/GM-CSF medium for differentiation into <t>immature</t> <t>moDC</t> in the absence (colored curves) or presence (gray curves) of AM-580, and expression levels of the indicated genes were measured by qPCR at the start of the cultivation (day 0) and on days 1, 2, 4, and 6. Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 0 and Wilcoxon test for comparison of both curves (Control vs. AM580). (E–H) Effect of tolerogenic compounds on gene expression in immature moDC by qPCR. Concentrations of compounds are provided in the Materials and Methods. Mean ± SEM of maximum 5 independent measurements; Friedman test (followed by Dunn’s multiple comparison test). (I) Analysis of ALDH1A2, RARa, and RARg expression by qPCR. Mean ± SEM; n = 6; Friedman test (followed by Dunn’s multiple comparison test). (J) Expression levels of three discrete ANKRD55 splice variants 201, 202, and 204 in immature moDC. Mean ± SEM; n = 10; Wilcoxon test. (K) Classical (Cla; CD14hi/CD16-), intermediate (Int; CD14hi/CD16+), and non- classical <t>(NC;</t> <t>CD14+/CD16+)</t> monocytes were isolated and separately cultivated for 6 days to differentiate into moDC. Gene expression levels were measured in the original monocyte subsets (M) and derived moDC (D). Mean ± SEM; n = 3; Mann–Whitney test for comparison between monocytes and moDC for each gene and subset. *p ≤0.05, **p ≤0.01.
Mo Dc Differentiation Inspector Antibody Cocktail, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/pm35111166-91-8-13?v=Miltenyi+Biotec
Average 97 stars, based on 1 article reviews
mo dc differentiation inspector antibody cocktail - by Bioz Stars, 2026-07
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cd209 dc sign microbeads  (Miltenyi Biotec)
91
Miltenyi Biotec cd209 dc sign microbeads
FIGURE 2 | Expression of ANKRD55 and neighboring genes in immature moDC. (A–D) Monocytes were cultivated for 6 days in IL-4/GM-CSF medium for differentiation into <t>immature</t> <t>moDC</t> in the absence (colored curves) or presence (gray curves) of AM-580, and expression levels of the indicated genes were measured by qPCR at the start of the cultivation (day 0) and on days 1, 2, 4, and 6. Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 0 and Wilcoxon test for comparison of both curves (Control vs. AM580). (E–H) Effect of tolerogenic compounds on gene expression in immature moDC by qPCR. Concentrations of compounds are provided in the Materials and Methods. Mean ± SEM of maximum 5 independent measurements; Friedman test (followed by Dunn’s multiple comparison test). (I) Analysis of ALDH1A2, RARa, and RARg expression by qPCR. Mean ± SEM; n = 6; Friedman test (followed by Dunn’s multiple comparison test). (J) Expression levels of three discrete ANKRD55 splice variants 201, 202, and 204 in immature moDC. Mean ± SEM; n = 10; Wilcoxon test. (K) Classical (Cla; CD14hi/CD16-), intermediate (Int; CD14hi/CD16+), and non- classical <t>(NC;</t> <t>CD14+/CD16+)</t> monocytes were isolated and separately cultivated for 6 days to differentiate into moDC. Gene expression levels were measured in the original monocyte subsets (M) and derived moDC (D). Mean ± SEM; n = 3; Mann–Whitney test for comparison between monocytes and moDC for each gene and subset. *p ≤0.05, **p ≤0.01.
Cd209 Dc Sign Microbeads, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/pmc08402705-62-20-23?v=Miltenyi+Biotec
Average 91 stars, based on 1 article reviews
cd209 dc sign microbeads - by Bioz Stars, 2026-07
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core solution  (Chem Impex International)
95
Chem Impex International core solution
FIGURE 2 | Expression of ANKRD55 and neighboring genes in immature moDC. (A–D) Monocytes were cultivated for 6 days in IL-4/GM-CSF medium for differentiation into <t>immature</t> <t>moDC</t> in the absence (colored curves) or presence (gray curves) of AM-580, and expression levels of the indicated genes were measured by qPCR at the start of the cultivation (day 0) and on days 1, 2, 4, and 6. Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 0 and Wilcoxon test for comparison of both curves (Control vs. AM580). (E–H) Effect of tolerogenic compounds on gene expression in immature moDC by qPCR. Concentrations of compounds are provided in the Materials and Methods. Mean ± SEM of maximum 5 independent measurements; Friedman test (followed by Dunn’s multiple comparison test). (I) Analysis of ALDH1A2, RARa, and RARg expression by qPCR. Mean ± SEM; n = 6; Friedman test (followed by Dunn’s multiple comparison test). (J) Expression levels of three discrete ANKRD55 splice variants 201, 202, and 204 in immature moDC. Mean ± SEM; n = 10; Wilcoxon test. (K) Classical (Cla; CD14hi/CD16-), intermediate (Int; CD14hi/CD16+), and non- classical <t>(NC;</t> <t>CD14+/CD16+)</t> monocytes were isolated and separately cultivated for 6 days to differentiate into moDC. Gene expression levels were measured in the original monocyte subsets (M) and derived moDC (D). Mean ± SEM; n = 3; Mann–Whitney test for comparison between monocytes and moDC for each gene and subset. *p ≤0.05, **p ≤0.01.
Core Solution, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/bio_rxiv__2025__04__03__647129-76-1-9?v=Chem+Impex+International
Average 95 stars, based on 1 article reviews
core solution - by Bioz Stars, 2026-07
95/100 stars
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soluble il 1 receptor ii elisa kit  (Hycult Biotech)
85
Hycult Biotech soluble il 1 receptor ii elisa kit
FIGURE 2 | Expression of ANKRD55 and neighboring genes in immature moDC. (A–D) Monocytes were cultivated for 6 days in IL-4/GM-CSF medium for differentiation into <t>immature</t> <t>moDC</t> in the absence (colored curves) or presence (gray curves) of AM-580, and expression levels of the indicated genes were measured by qPCR at the start of the cultivation (day 0) and on days 1, 2, 4, and 6. Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 0 and Wilcoxon test for comparison of both curves (Control vs. AM580). (E–H) Effect of tolerogenic compounds on gene expression in immature moDC by qPCR. Concentrations of compounds are provided in the Materials and Methods. Mean ± SEM of maximum 5 independent measurements; Friedman test (followed by Dunn’s multiple comparison test). (I) Analysis of ALDH1A2, RARa, and RARg expression by qPCR. Mean ± SEM; n = 6; Friedman test (followed by Dunn’s multiple comparison test). (J) Expression levels of three discrete ANKRD55 splice variants 201, 202, and 204 in immature moDC. Mean ± SEM; n = 10; Wilcoxon test. (K) Classical (Cla; CD14hi/CD16-), intermediate (Int; CD14hi/CD16+), and non- classical <t>(NC;</t> <t>CD14+/CD16+)</t> monocytes were isolated and separately cultivated for 6 days to differentiate into moDC. Gene expression levels were measured in the original monocyte subsets (M) and derived moDC (D). Mean ± SEM; n = 3; Mann–Whitney test for comparison between monocytes and moDC for each gene and subset. *p ≤0.05, **p ≤0.01.
Soluble Il 1 Receptor Ii Elisa Kit, supplied by Hycult Biotech, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dc+assay+kit/10__1017_slash_s0007114509991930-40-2-8?v=Hycult+Biotech
Average 85 stars, based on 1 article reviews
soluble il 1 receptor ii elisa kit - by Bioz Stars, 2026-07
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Image Search Results


FIGURE 2 | Expression of ANKRD55 and neighboring genes in immature moDC. (A–D) Monocytes were cultivated for 6 days in IL-4/GM-CSF medium for differentiation into immature moDC in the absence (colored curves) or presence (gray curves) of AM-580, and expression levels of the indicated genes were measured by qPCR at the start of the cultivation (day 0) and on days 1, 2, 4, and 6. Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 0 and Wilcoxon test for comparison of both curves (Control vs. AM580). (E–H) Effect of tolerogenic compounds on gene expression in immature moDC by qPCR. Concentrations of compounds are provided in the Materials and Methods. Mean ± SEM of maximum 5 independent measurements; Friedman test (followed by Dunn’s multiple comparison test). (I) Analysis of ALDH1A2, RARa, and RARg expression by qPCR. Mean ± SEM; n = 6; Friedman test (followed by Dunn’s multiple comparison test). (J) Expression levels of three discrete ANKRD55 splice variants 201, 202, and 204 in immature moDC. Mean ± SEM; n = 10; Wilcoxon test. (K) Classical (Cla; CD14hi/CD16-), intermediate (Int; CD14hi/CD16+), and non- classical (NC; CD14+/CD16+) monocytes were isolated and separately cultivated for 6 days to differentiate into moDC. Gene expression levels were measured in the original monocyte subsets (M) and derived moDC (D). Mean ± SEM; n = 3; Mann–Whitney test for comparison between monocytes and moDC for each gene and subset. *p ≤0.05, **p ≤0.01.

Journal: Frontiers in immunology

Article Title: Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55 - IL6ST Gene Region in Immature Dendritic Cells.

doi: 10.3389/fimmu.2021.816930

Figure Lengend Snippet: FIGURE 2 | Expression of ANKRD55 and neighboring genes in immature moDC. (A–D) Monocytes were cultivated for 6 days in IL-4/GM-CSF medium for differentiation into immature moDC in the absence (colored curves) or presence (gray curves) of AM-580, and expression levels of the indicated genes were measured by qPCR at the start of the cultivation (day 0) and on days 1, 2, 4, and 6. Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 0 and Wilcoxon test for comparison of both curves (Control vs. AM580). (E–H) Effect of tolerogenic compounds on gene expression in immature moDC by qPCR. Concentrations of compounds are provided in the Materials and Methods. Mean ± SEM of maximum 5 independent measurements; Friedman test (followed by Dunn’s multiple comparison test). (I) Analysis of ALDH1A2, RARa, and RARg expression by qPCR. Mean ± SEM; n = 6; Friedman test (followed by Dunn’s multiple comparison test). (J) Expression levels of three discrete ANKRD55 splice variants 201, 202, and 204 in immature moDC. Mean ± SEM; n = 10; Wilcoxon test. (K) Classical (Cla; CD14hi/CD16-), intermediate (Int; CD14hi/CD16+), and non- classical (NC; CD14+/CD16+) monocytes were isolated and separately cultivated for 6 days to differentiate into moDC. Gene expression levels were measured in the original monocyte subsets (M) and derived moDC (D). Mean ± SEM; n = 3; Mann–Whitney test for comparison between monocytes and moDC for each gene and subset. *p ≤0.05, **p ≤0.01.

Article Snippet: For evaluation of maturation, cells were analyzed with Mo–DC Differentiation Inspector antibody cocktail [Miltenyi Biotec, Ref. 130-093-567; antihuman CD14-FITC antibody (clone Tük4, isotype: mouse IgG2a), anti-human CD83-APC (clone: HB15, isotype: mouse IgG1), and anti-human CD209-PE (clone DCN-47.5.4, isotype: mouse IgG1)] or isotype control cocktail following manufacturer’s instructions and analyzed on a MACSQuant® flow cytometer (Miltenyi Biotec).

Techniques: Expressing, Comparison, Control, Gene Expression, Isolation, Derivative Assay, MANN-WHITNEY

FIGURE 3 | Effect of maturation of moDC on the expression of ANKRD55, IL6ST, IL31RA, and SLC38A9. (A) Comparison of the effect of maturation by CpG, poly(I: C)/LPS and IFN-g/LPS on expression levels of the main ANKRD55 splice variants by qPCR. Mean ± SEM; n = 3; Friedman test (followed by Dunn’s multiple comparison test). (B) Flow cytometry to assess the maturation percentage induced by the indicated stimuli based on the expression of CD209 (expressed in moDC) and CD83 (expressed in mature moDC only). Shown is a representative experiment out of 4 performed. (C–F) MoDCs cultivated for 5 days in MoDC medium were matured by addition of IFN-g and 24 h later LPS. Gene expression was analyzed by qPCR coinciding with time of IFN-g (day 5) and LPS (0 h) addition and 3, 6, 12, 24, and 48 h later. The experiment was also performed in cells differentiated in the presence of AM-580 (gray curves). Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 5 and Wilcoxon test for comparison of both curves (control vs. AM580). *p ≤0.05, **p ≤0.01.

Journal: Frontiers in immunology

Article Title: Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55 - IL6ST Gene Region in Immature Dendritic Cells.

doi: 10.3389/fimmu.2021.816930

Figure Lengend Snippet: FIGURE 3 | Effect of maturation of moDC on the expression of ANKRD55, IL6ST, IL31RA, and SLC38A9. (A) Comparison of the effect of maturation by CpG, poly(I: C)/LPS and IFN-g/LPS on expression levels of the main ANKRD55 splice variants by qPCR. Mean ± SEM; n = 3; Friedman test (followed by Dunn’s multiple comparison test). (B) Flow cytometry to assess the maturation percentage induced by the indicated stimuli based on the expression of CD209 (expressed in moDC) and CD83 (expressed in mature moDC only). Shown is a representative experiment out of 4 performed. (C–F) MoDCs cultivated for 5 days in MoDC medium were matured by addition of IFN-g and 24 h later LPS. Gene expression was analyzed by qPCR coinciding with time of IFN-g (day 5) and LPS (0 h) addition and 3, 6, 12, 24, and 48 h later. The experiment was also performed in cells differentiated in the presence of AM-580 (gray curves). Mean ± SEM of 3 independent measurements; Friedman test (followed by Dunn’s multiple comparison test) for comparison of data points in each curve with day 5 and Wilcoxon test for comparison of both curves (control vs. AM580). *p ≤0.05, **p ≤0.01.

Article Snippet: For evaluation of maturation, cells were analyzed with Mo–DC Differentiation Inspector antibody cocktail [Miltenyi Biotec, Ref. 130-093-567; antihuman CD14-FITC antibody (clone Tük4, isotype: mouse IgG2a), anti-human CD83-APC (clone: HB15, isotype: mouse IgG1), and anti-human CD209-PE (clone DCN-47.5.4, isotype: mouse IgG1)] or isotype control cocktail following manufacturer’s instructions and analyzed on a MACSQuant® flow cytometer (Miltenyi Biotec).

Techniques: Expressing, Comparison, Flow Cytometry, Gene Expression, Control

FIGURE 5 | Digital droplet PCR (ddPCR) quantification of gene transcript copy numbers in pDC, mDC, CD14+ monocytes, PBMC fraction minus monocytes (F-), and moDC. Analysis was performed in 350 pg cDNA (A, E, F) or 30 ng of cDNA (B–D). (C) ddPCR quantification of ANKRD55 transcript copy numbers in moDC treated with AM-580. (D) ANKRD55 copy numbers in moDC matured or not with IFN-g/LPS measured at 6 h after addition of stimulus. (F) Transcript levels of markers specific for mDC (CD1c) and pDC (IL3RA, CLEC4C).

Journal: Frontiers in immunology

Article Title: Genomic Multiple Sclerosis Risk Variants Modulate the Expression of the ANKRD55 - IL6ST Gene Region in Immature Dendritic Cells.

doi: 10.3389/fimmu.2021.816930

Figure Lengend Snippet: FIGURE 5 | Digital droplet PCR (ddPCR) quantification of gene transcript copy numbers in pDC, mDC, CD14+ monocytes, PBMC fraction minus monocytes (F-), and moDC. Analysis was performed in 350 pg cDNA (A, E, F) or 30 ng of cDNA (B–D). (C) ddPCR quantification of ANKRD55 transcript copy numbers in moDC treated with AM-580. (D) ANKRD55 copy numbers in moDC matured or not with IFN-g/LPS measured at 6 h after addition of stimulus. (F) Transcript levels of markers specific for mDC (CD1c) and pDC (IL3RA, CLEC4C).

Article Snippet: For evaluation of maturation, cells were analyzed with Mo–DC Differentiation Inspector antibody cocktail [Miltenyi Biotec, Ref. 130-093-567; antihuman CD14-FITC antibody (clone Tük4, isotype: mouse IgG2a), anti-human CD83-APC (clone: HB15, isotype: mouse IgG1), and anti-human CD209-PE (clone DCN-47.5.4, isotype: mouse IgG1)] or isotype control cocktail following manufacturer’s instructions and analyzed on a MACSQuant® flow cytometer (Miltenyi Biotec).

Techniques: