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anti cd54 apc  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec anti cd54 apc
    Anti Cd54 Apc, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 35 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd54+apc/CD54+(ICAM-1)+Antibody%2C+anti-human%2C+REAfinity/pm41864987-137-11-16
    Average 94 stars, based on 35 article reviews
    anti cd54 apc - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Staining:

    Article Title: A human 3D immune competent full-thickness skin model mimicking dermal dendritic cell activation.
    Article Snippet: .. For staining the cells were incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi, #130-113- 444), REA Control (S)-PE (Miltenyi, #130-113-438), REA Control (S)-APC (Miltenyi, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi, #130-113-440); CD54-APC (Miltenyi, #130-121-342); CD86-APC (Miltenyi, #130-116-161), CD14-VioGreen (Miltenyi, #130-110-525), CD11c-APC (Miltenyi, #130-113-584) for 10 minutes in the dark. .. For single cells from the dissociates skin models the following antibodies were used (1:50): CD45-VioBright R667 (Miltenyi, ##130-110-779), CD54-PE-Vio770 (Miltenyi, #130- 127-992), CD86-PE-Vio770 (Miltenyi, #130-116-265).

    Article Title: The Monocytic Cell Line THP-1 as a Validated and Robust Surrogate Model for Human Dendritic Cells
    Article Snippet: .. Cells were stained with the following antibodies: diluted 1:50, REA Control (S)-VioGreen (Miltenyi Biotec, #130-113-444), REA Control (S)-PE (Miltenyi Biotec, #130-113-438), REA Control (S)-APC (Miltenyi Biotec, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi Biotec, #130-113-440); HLA-DR-VioGreen (Miltenyi Biotec, #130-111-795), CD54-APC (Miltenyi Biotec, #130-121-342); CXCR4-PE-Vio770 (Miltenyi Biotec, #130-116-161); CD11b-VioGreen (Miltenyi Biotec, #130-110-617); CD83-PE (Miltenyi Biotec, #130-110-561); CD86-APC (Miltenyi Biotec, #130-116-161) for 10 min at 4 °C in the dark. .. Afterwards, cells were washed thrice with autoMACS running buffer and stained with DAPI (Sigma, #D9542), to exclude dead cells for the determination of the cell viability.

    Article Title: A human 3D immune competent full-thickness skin model mimicking dermal dendritic cell activation
    Article Snippet: .. For staining the cells were incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi, #130-113-444), REA Control (S)-PE (Miltenyi, #130-113-438), REA Control (S)-APC (Miltenyi, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi, #130-113-440); CD54-APC (Miltenyi, #130-121-342); CD86-APC (Miltenyi, #130-116-161), CD14-VioGreen (Miltenyi, #130-110-525), CD11c-APC (Miltenyi, #130-113-584) for 10 minutes in the dark. .. For single cells from the dissociates skin models the following antibodies were used (1:50): CD45-VioBright R667 (Miltenyi, ##130-110-779), CD54-PE-Vio770 (Miltenyi, #130-127-992), CD86-PE-Vio770 (Miltenyi, #130-116-265).

    Article Title: Extensive monolayer formation depends on a subpopulation of transplanted human iPSC-derived RPE cells
    Article Snippet: .. P1 cells were stained with CD54-APC (Miltenyi, 130-121-342) and PSA-NCAM-PE (Miltenyi, 130-117-394) according to data sheet. ..

    Article Title: Pseudopterosin A-D Modulates Dendritic Cell Activation in Skin Sensitization
    Article Snippet: After 24 h, cells were harvested, washed three times in autoMACS running buffer (Miltenyi Biotec, #130-091-221, Gladbach, Germany), and transferred to 96-well plates (2 × 10 5 cells per antibody panel). .. Cells were stained with the following antibodies (diluted 1:50) for 10 min at 4 °C in the dark: REA Control (S)-APC (Miltenyi Biotec, #130-113-434), CD54-APC (Miltenyi Biotec, #130-121-342), and CD86-APC (Miltenyi Biotec, #130-116-161). .. After staining, cells were washed three times with autoMACS running buffer and stained with DAPI (Sigma-Aldrich, #D9542, Darmstadt, Germany) to exclude dead cells and assess viability.

    Incubation:

    Article Title: A human 3D immune competent full-thickness skin model mimicking dermal dendritic cell activation.
    Article Snippet: .. For staining the cells were incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi, #130-113- 444), REA Control (S)-PE (Miltenyi, #130-113-438), REA Control (S)-APC (Miltenyi, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi, #130-113-440); CD54-APC (Miltenyi, #130-121-342); CD86-APC (Miltenyi, #130-116-161), CD14-VioGreen (Miltenyi, #130-110-525), CD11c-APC (Miltenyi, #130-113-584) for 10 minutes in the dark. .. For single cells from the dissociates skin models the following antibodies were used (1:50): CD45-VioBright R667 (Miltenyi, ##130-110-779), CD54-PE-Vio770 (Miltenyi, #130- 127-992), CD86-PE-Vio770 (Miltenyi, #130-116-265).

    Article Title: A human 3D immune competent full-thickness skin model mimicking dermal dendritic cell activation
    Article Snippet: .. For staining the cells were incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi, #130-113-444), REA Control (S)-PE (Miltenyi, #130-113-438), REA Control (S)-APC (Miltenyi, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi, #130-113-440); CD54-APC (Miltenyi, #130-121-342); CD86-APC (Miltenyi, #130-116-161), CD14-VioGreen (Miltenyi, #130-110-525), CD11c-APC (Miltenyi, #130-113-584) for 10 minutes in the dark. .. For single cells from the dissociates skin models the following antibodies were used (1:50): CD45-VioBright R667 (Miltenyi, ##130-110-779), CD54-PE-Vio770 (Miltenyi, #130-127-992), CD86-PE-Vio770 (Miltenyi, #130-116-265).

    Article Title: Incorporating immune cell surrogates into a full-thickness tissue equivalent of human skin to characterize dendritic cell activation.
    Article Snippet: Surface marker detection via flow cytometry Cells were harvested after differentiation or treatment and washed in autoMacs Running Buffer (Miltenyi Biotec, #130-091-221, Gladbach, Germany). .. At least 1 × 105 cells for each antibody panel were transferred to 96-well u-bottom plates and incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi Biotec, #130-113-444), REA Control (S)-PE (Miltenyi Biotec, #130-113-438), REA Control (S)-APC (Miltenyi Biotec, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi Biotec, #130- 113-440); HLA-DR-VioGreen (Miltenyi Biotec, #130-111-948), CD1a-PE (Miltenyi Biotec, #130-112-022); CD207-PE-Vio770 (Miltenyi Biotec, #130-112-370), CD54-APC (Miltenyi Biotec, #130-121-342); CD86-APC (Miltenyi Biotec, #130-116-161), CD83-PE (Miltenyi Biotec, #130-110-561), CD11b-VioGreen (Miltenyi Biotec, #130-110-617), CD11c-APC (Miltenyi Biotec, #130-113-584) for 10 min in the dark. ..

    Control:

    Article Title: A human 3D immune competent full-thickness skin model mimicking dermal dendritic cell activation.
    Article Snippet: .. For staining the cells were incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi, #130-113- 444), REA Control (S)-PE (Miltenyi, #130-113-438), REA Control (S)-APC (Miltenyi, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi, #130-113-440); CD54-APC (Miltenyi, #130-121-342); CD86-APC (Miltenyi, #130-116-161), CD14-VioGreen (Miltenyi, #130-110-525), CD11c-APC (Miltenyi, #130-113-584) for 10 minutes in the dark. .. For single cells from the dissociates skin models the following antibodies were used (1:50): CD45-VioBright R667 (Miltenyi, ##130-110-779), CD54-PE-Vio770 (Miltenyi, #130- 127-992), CD86-PE-Vio770 (Miltenyi, #130-116-265).

    Article Title: The Monocytic Cell Line THP-1 as a Validated and Robust Surrogate Model for Human Dendritic Cells
    Article Snippet: .. Cells were stained with the following antibodies: diluted 1:50, REA Control (S)-VioGreen (Miltenyi Biotec, #130-113-444), REA Control (S)-PE (Miltenyi Biotec, #130-113-438), REA Control (S)-APC (Miltenyi Biotec, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi Biotec, #130-113-440); HLA-DR-VioGreen (Miltenyi Biotec, #130-111-795), CD54-APC (Miltenyi Biotec, #130-121-342); CXCR4-PE-Vio770 (Miltenyi Biotec, #130-116-161); CD11b-VioGreen (Miltenyi Biotec, #130-110-617); CD83-PE (Miltenyi Biotec, #130-110-561); CD86-APC (Miltenyi Biotec, #130-116-161) for 10 min at 4 °C in the dark. .. Afterwards, cells were washed thrice with autoMACS running buffer and stained with DAPI (Sigma, #D9542), to exclude dead cells for the determination of the cell viability.

    Article Title: A human 3D immune competent full-thickness skin model mimicking dermal dendritic cell activation
    Article Snippet: .. For staining the cells were incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi, #130-113-444), REA Control (S)-PE (Miltenyi, #130-113-438), REA Control (S)-APC (Miltenyi, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi, #130-113-440); CD54-APC (Miltenyi, #130-121-342); CD86-APC (Miltenyi, #130-116-161), CD14-VioGreen (Miltenyi, #130-110-525), CD11c-APC (Miltenyi, #130-113-584) for 10 minutes in the dark. .. For single cells from the dissociates skin models the following antibodies were used (1:50): CD45-VioBright R667 (Miltenyi, ##130-110-779), CD54-PE-Vio770 (Miltenyi, #130-127-992), CD86-PE-Vio770 (Miltenyi, #130-116-265).

    Article Title: Incorporating immune cell surrogates into a full-thickness tissue equivalent of human skin to characterize dendritic cell activation.
    Article Snippet: Surface marker detection via flow cytometry Cells were harvested after differentiation or treatment and washed in autoMacs Running Buffer (Miltenyi Biotec, #130-091-221, Gladbach, Germany). .. At least 1 × 105 cells for each antibody panel were transferred to 96-well u-bottom plates and incubated in Automacs Running Buffer with the following antibodies (1:50): REA Control (S)-VioGreen (Miltenyi Biotec, #130-113-444), REA Control (S)-PE (Miltenyi Biotec, #130-113-438), REA Control (S)-APC (Miltenyi Biotec, #130-113-434); REA Control (S)-PE-Vio770, (Miltenyi Biotec, #130- 113-440); HLA-DR-VioGreen (Miltenyi Biotec, #130-111-948), CD1a-PE (Miltenyi Biotec, #130-112-022); CD207-PE-Vio770 (Miltenyi Biotec, #130-112-370), CD54-APC (Miltenyi Biotec, #130-121-342); CD86-APC (Miltenyi Biotec, #130-116-161), CD83-PE (Miltenyi Biotec, #130-110-561), CD11b-VioGreen (Miltenyi Biotec, #130-110-617), CD11c-APC (Miltenyi Biotec, #130-113-584) for 10 min in the dark. ..

    Article Title: Pseudopterosin A-D Modulates Dendritic Cell Activation in Skin Sensitization
    Article Snippet: After 24 h, cells were harvested, washed three times in autoMACS running buffer (Miltenyi Biotec, #130-091-221, Gladbach, Germany), and transferred to 96-well plates (2 × 10 5 cells per antibody panel). .. Cells were stained with the following antibodies (diluted 1:50) for 10 min at 4 °C in the dark: REA Control (S)-APC (Miltenyi Biotec, #130-113-434), CD54-APC (Miltenyi Biotec, #130-121-342), and CD86-APC (Miltenyi Biotec, #130-116-161). .. After staining, cells were washed three times with autoMACS running buffer and stained with DAPI (Sigma-Aldrich, #D9542, Darmstadt, Germany) to exclude dead cells and assess viability.

    Blocking Assay:

    Article Title: Multiparametric in vitro and in vivo analysis of the safety profile of self-assembling peptides.
    Article Snippet: Nickel Sulphate (NiSO4, Sigma-Aldrich, 656895), 2,4-dinitrochlorobenzene (DNCB; Sigma-Aldrich, 237329), and lactic acid (LA, Sigma-Aldrich, PHR1215) were purchased from Sigma-Aldrich and selected based upon the criteria detailed in the general guidance from Organisation for Economic Cooperation and Development (OECD). .. The fluorophore-conjugated antibodies CD86-PE and CD54-APC were obtained from Miltenyi Biotec and Fc Block from BD. .. All reagents (sodium dodecyl sulfate (SDS), hydroxide sodium (NaOH)) and solvents (hexafluoroisopropanol (HFIP), trifluoroacetic acid (TFA), dimethyl formamide (DMF), hydrochloric acid (HCl) and ethanol (EtOH)) were purchased from Merck (Merck Millipore, Darmstadt, Germany), Sigma Aldrich (Sigma Aldrich Chemie GmbH, München, Germany) and VWR (Radnor, PA, USA) in highest quality commercially available and used as received.



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    Pseudoperosin (Ps)A-D reduces the nickel sulfate (NiSO 4 ) induced upregulation of DC activation markers <t>CD54</t> and CD86 in a similar manner as dexamethasone. THP-1-derived dermal dendritic cell surrogates (DDCs) were seeded with 1 × 10 6 cells/mL into a 24-well plate. Cells were pre-treated with dexamethasone [1 µM] or PsA-D [20 µM] for 1 h, followed by NiSO 4 [380 µM] treatment for 23 h. Surface marker analysis was performed via flow cytometry and is depicted as histograms ( A ) and percentage of positive cells ( B ). Error bars indicate the standard errors of the mean ( n = 3 independent experiments with * = p ≤ 0.05 and ** = p ≤ 0.01).
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    Image Search Results


    A) Schematic of genome-wide CRISPRi screen identifying CD54 (ICAM-1) regulators. K-562 CRISPRi cells were infected with a guide RNA library at MOI 0.3 and 5, then sorted into three bins (low/high 10%, mid 20%) based on CD54 antibody staining. The screen was conducted at three different library representation levels. B) Analytic flow cytometry of sorted cell populations. C) CRISPRi screen hits showing positive regulators (CD54 low bin) and negative regulators (CD54 high bin) of CD54. MAGeCK scores across all experimental conditions are displayed for individually validated hits. D) Pearson correlation of samples with varying cell coverage, based on log 2 fold changes of normalized sgRNA abundances between low and mid CD54 populations. E) Percentage of shared hits between samples with varying cell coverage within the MOI 0.3 and MOI 5 condition. F) Hits selected across all conditions were individually validated to calculate true positive rate (TPR) and accuracy to identify hits.

    Journal: bioRxiv

    Article Title: Multiplexed Perturbation Enables Scalable Pooled Screens

    doi: 10.1101/2025.08.14.669942

    Figure Lengend Snippet: A) Schematic of genome-wide CRISPRi screen identifying CD54 (ICAM-1) regulators. K-562 CRISPRi cells were infected with a guide RNA library at MOI 0.3 and 5, then sorted into three bins (low/high 10%, mid 20%) based on CD54 antibody staining. The screen was conducted at three different library representation levels. B) Analytic flow cytometry of sorted cell populations. C) CRISPRi screen hits showing positive regulators (CD54 low bin) and negative regulators (CD54 high bin) of CD54. MAGeCK scores across all experimental conditions are displayed for individually validated hits. D) Pearson correlation of samples with varying cell coverage, based on log 2 fold changes of normalized sgRNA abundances between low and mid CD54 populations. E) Percentage of shared hits between samples with varying cell coverage within the MOI 0.3 and MOI 5 condition. F) Hits selected across all conditions were individually validated to calculate true positive rate (TPR) and accuracy to identify hits.

    Article Snippet: After lentiviral transduction and puromycin selection, live cells were stained with an APC-coupled antibody against CD54 (Miltenyi Biotec) in EasySep buffer for 30 min on ice.

    Techniques: Genome Wide, Infection, Staining, Flow Cytometry

    A) Screen results showing guide RNA enrichments based on CD54 levels comparing the bottom 10% of cells to the middle 20% (low vs. mid) or comparing the top 10% to the middle 20% (high vs. mid). False discovery rates (FDR) are shown against log10 transformed MAGeCK scores. Genes are ranked by their MAGeCK score. Results from highest cell number (250X) screens are shown here. Ranking of screen hits based on MAGeCK scores for low vs. mid (B) and high vs. mid (C) comparisons. E) Hits identified in the highest cell number sample (250x) are partitioned into quartiles based on their MAGeCK score in the low CD54 vs. mid CD54 comparison. The most enriched hits are represented in quartile 1 and the least enriched hits in quartile 4. False discovery rates (FDR) of these are shown across different conditions. (Box represents the interquartile range (IQR), spanning from the first to the third quartile, line indicates the median and whiskers extend to 1.5 times the IQR) F) Euclidean distances comparing samples with different cell coverage based on log 2 fold changes of normalized sgRNA abundances (top). Pearson correlation of the same comparison restricted to genes identified as significant hits in any of the conditions (bottom). G) Percentage of shared hits between cell number settings within the MOI 0.3 and MOI 5 condition in the high CD54 vs. mid CD54 comparison. H) As in (E) but based on the comparison high CD54 vs. mid CD54. Hits identified in the highest cell number sample (250x) are partitioned into quartiles based on their MAGeCK score. The most enriched hits are represented in quartile 1 and the least enriched hits in quartile 4. False discovery rates (FDR) of these are shown across different conditions. True-positive rate (TPR) and false-positive rate (FPR) across all conditions. Sample colors are as in (I).

    Journal: bioRxiv

    Article Title: Multiplexed Perturbation Enables Scalable Pooled Screens

    doi: 10.1101/2025.08.14.669942

    Figure Lengend Snippet: A) Screen results showing guide RNA enrichments based on CD54 levels comparing the bottom 10% of cells to the middle 20% (low vs. mid) or comparing the top 10% to the middle 20% (high vs. mid). False discovery rates (FDR) are shown against log10 transformed MAGeCK scores. Genes are ranked by their MAGeCK score. Results from highest cell number (250X) screens are shown here. Ranking of screen hits based on MAGeCK scores for low vs. mid (B) and high vs. mid (C) comparisons. E) Hits identified in the highest cell number sample (250x) are partitioned into quartiles based on their MAGeCK score in the low CD54 vs. mid CD54 comparison. The most enriched hits are represented in quartile 1 and the least enriched hits in quartile 4. False discovery rates (FDR) of these are shown across different conditions. (Box represents the interquartile range (IQR), spanning from the first to the third quartile, line indicates the median and whiskers extend to 1.5 times the IQR) F) Euclidean distances comparing samples with different cell coverage based on log 2 fold changes of normalized sgRNA abundances (top). Pearson correlation of the same comparison restricted to genes identified as significant hits in any of the conditions (bottom). G) Percentage of shared hits between cell number settings within the MOI 0.3 and MOI 5 condition in the high CD54 vs. mid CD54 comparison. H) As in (E) but based on the comparison high CD54 vs. mid CD54. Hits identified in the highest cell number sample (250x) are partitioned into quartiles based on their MAGeCK score. The most enriched hits are represented in quartile 1 and the least enriched hits in quartile 4. False discovery rates (FDR) of these are shown across different conditions. True-positive rate (TPR) and false-positive rate (FPR) across all conditions. Sample colors are as in (I).

    Article Snippet: After lentiviral transduction and puromycin selection, live cells were stained with an APC-coupled antibody against CD54 (Miltenyi Biotec) in EasySep buffer for 30 min on ice.

    Techniques: Transformation Assay, Comparison

    Pseudoperosin (Ps)A-D reduces the nickel sulfate (NiSO 4 ) induced upregulation of DC activation markers CD54 and CD86 in a similar manner as dexamethasone. THP-1-derived dermal dendritic cell surrogates (DDCs) were seeded with 1 × 10 6 cells/mL into a 24-well plate. Cells were pre-treated with dexamethasone [1 µM] or PsA-D [20 µM] for 1 h, followed by NiSO 4 [380 µM] treatment for 23 h. Surface marker analysis was performed via flow cytometry and is depicted as histograms ( A ) and percentage of positive cells ( B ). Error bars indicate the standard errors of the mean ( n = 3 independent experiments with * = p ≤ 0.05 and ** = p ≤ 0.01).

    Journal: Marine Drugs

    Article Title: Pseudopterosin A-D Modulates Dendritic Cell Activation in Skin Sensitization

    doi: 10.3390/md23060245

    Figure Lengend Snippet: Pseudoperosin (Ps)A-D reduces the nickel sulfate (NiSO 4 ) induced upregulation of DC activation markers CD54 and CD86 in a similar manner as dexamethasone. THP-1-derived dermal dendritic cell surrogates (DDCs) were seeded with 1 × 10 6 cells/mL into a 24-well plate. Cells were pre-treated with dexamethasone [1 µM] or PsA-D [20 µM] for 1 h, followed by NiSO 4 [380 µM] treatment for 23 h. Surface marker analysis was performed via flow cytometry and is depicted as histograms ( A ) and percentage of positive cells ( B ). Error bars indicate the standard errors of the mean ( n = 3 independent experiments with * = p ≤ 0.05 and ** = p ≤ 0.01).

    Article Snippet: Cells were stained with the following antibodies (diluted 1:50) for 10 min at 4 °C in the dark: REA Control (S)-APC (Miltenyi Biotec, #130-113-434), CD54-APC (Miltenyi Biotec, #130-121-342), and CD86-APC (Miltenyi Biotec, #130-116-161).

    Techniques: Activation Assay, Derivative Assay, Marker, Flow Cytometry