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mouse anti human cd14 fitc  (Bio-Rad)


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    Structured Review

    Bio-Rad mouse anti human cd14 fitc
    Mouse Anti Human Cd14 Fitc, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 95/100, based on 279 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti human cd14 fitc/product/Bio-Rad
    Average 95 stars, based on 279 article reviews
    mouse anti human cd14 fitc - by Bioz Stars, 2026-03
    95/100 stars

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    The results of THP-1 cell sorting using a flow cytometer with <t>CD14-FITC</t> labeling for cell sorting. ( A – C ) represent the gating strategy employed during the sorting of PMA-induced THP-1 cells, labeled as Gate 1 to Gate 3. ( D ) displays a peak map illustrating the cellular composition and distribution resulting from the sorting of PMA-induced THP-1 cells. ( E ) presents the percentage composition of FITC-positive cells obtained from the sorting of PMA-induced THP-1 cells. Similarly, ( F – H ) depict the gating strategy utilized during the sorting of THP-1 cells in the control group. ( I ) exhibits a peak map illustrating the cellular composition and distribution resulting from the sorting of THP-1 cells in the control group. Finally, ( J ) provides the percentage composition of FITC-positive cells obtained from the sorting of THP-1 cells in the control group.
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    Details of the antibodies used in this study.

    Journal: Scientific Reports

    Article Title: Identification of organs of origin of macrophages that produce presepsin via neutrophil extracellular trap phagocytosis

    doi: 10.1038/s41598-024-66916-y

    Figure Lengend Snippet: Details of the antibodies used in this study.

    Article Snippet: FITC-labeled anti-human CD14 mouse monoclonal antibody , Cat. No. 6603511; Beckman Coulter, Brea, CA, USA.

    Techniques:

    PMA induced THP-1 cell differentiation. ( A ) Flow cytometric determination of the CD11b+ THP-1 cell proportion. ( B ) The CD11b statistical histogram. ( C ) Flow cytometric determination of the CD14+ THP-1 cell proportion. ( D ) The CD14 statistical histogram. ( E ) CD11b and ( F ) CD14 immunofluorescence intensity in THP-1 cells. Normal distribution, ANOVA test, * P < 0.05, **** P < 0.0001.

    Journal: Aging (Albany NY)

    Article Title: The miR-146b-3p/TNFAIP2 axis regulates cell differentiation in acute myeloid leukaemia

    doi: 10.18632/aging.205441

    Figure Lengend Snippet: PMA induced THP-1 cell differentiation. ( A ) Flow cytometric determination of the CD11b+ THP-1 cell proportion. ( B ) The CD11b statistical histogram. ( C ) Flow cytometric determination of the CD14+ THP-1 cell proportion. ( D ) The CD14 statistical histogram. ( E ) CD11b and ( F ) CD14 immunofluorescence intensity in THP-1 cells. Normal distribution, ANOVA test, * P < 0.05, **** P < 0.0001.

    Article Snippet: Cell differentiation was assessed using immunofluorescence staining with a PE-conjugated mouse anti-human CD11b antibody and an FITC-conjugated mouse anti-human CD14 antibody (BD Bioscience, USA).

    Techniques: Cell Differentiation, Immunofluorescence

    Forced expression of TNFAIP2 significantly induced the differentiation of MOLM-13 cells. ( A ) Flow cytometric determination of the CD11b+ cell proportion in transduced MOLM-13 cells. ( B ) The CD11b statistical histogram. ( C ) Flow cytometric determination of the CD14+ cell proportion in transduced MOLM-13 cells. ( D ) The CD14 statistical histogram. ( E ) The immunofluorescence intensity of CD11b and CD14 in transduced MOLM-13 cells. Normal distribution, t test, ** P < 0.01.

    Journal: Aging (Albany NY)

    Article Title: The miR-146b-3p/TNFAIP2 axis regulates cell differentiation in acute myeloid leukaemia

    doi: 10.18632/aging.205441

    Figure Lengend Snippet: Forced expression of TNFAIP2 significantly induced the differentiation of MOLM-13 cells. ( A ) Flow cytometric determination of the CD11b+ cell proportion in transduced MOLM-13 cells. ( B ) The CD11b statistical histogram. ( C ) Flow cytometric determination of the CD14+ cell proportion in transduced MOLM-13 cells. ( D ) The CD14 statistical histogram. ( E ) The immunofluorescence intensity of CD11b and CD14 in transduced MOLM-13 cells. Normal distribution, t test, ** P < 0.01.

    Article Snippet: Cell differentiation was assessed using immunofluorescence staining with a PE-conjugated mouse anti-human CD11b antibody and an FITC-conjugated mouse anti-human CD14 antibody (BD Bioscience, USA).

    Techniques: Expressing, Immunofluorescence

    Knockdown of miR-146b-3p significantly induced the differentiation of MOLM-13 cells. ( A ) Flow cytometric determination of the CD11b+ cell proportion in transduced MOLM-13 cells. ( B ) The CD11b statistical histogram. ( C ) Flow cytometric determination of the CD14+ cell proportion in transduced MOLM-13 cells. ( D ) The CD14 statistical histogram. ( E ) The immunofluorescence intensity of CD11b and CD14 in transduced MOLM-13 cells. Normal distribution, t test, ** P < 0.01.

    Journal: Aging (Albany NY)

    Article Title: The miR-146b-3p/TNFAIP2 axis regulates cell differentiation in acute myeloid leukaemia

    doi: 10.18632/aging.205441

    Figure Lengend Snippet: Knockdown of miR-146b-3p significantly induced the differentiation of MOLM-13 cells. ( A ) Flow cytometric determination of the CD11b+ cell proportion in transduced MOLM-13 cells. ( B ) The CD11b statistical histogram. ( C ) Flow cytometric determination of the CD14+ cell proportion in transduced MOLM-13 cells. ( D ) The CD14 statistical histogram. ( E ) The immunofluorescence intensity of CD11b and CD14 in transduced MOLM-13 cells. Normal distribution, t test, ** P < 0.01.

    Article Snippet: Cell differentiation was assessed using immunofluorescence staining with a PE-conjugated mouse anti-human CD11b antibody and an FITC-conjugated mouse anti-human CD14 antibody (BD Bioscience, USA).

    Techniques: Immunofluorescence

    The results of THP-1 cell sorting using a flow cytometer with CD14-FITC labeling for cell sorting. ( A – C ) represent the gating strategy employed during the sorting of PMA-induced THP-1 cells, labeled as Gate 1 to Gate 3. ( D ) displays a peak map illustrating the cellular composition and distribution resulting from the sorting of PMA-induced THP-1 cells. ( E ) presents the percentage composition of FITC-positive cells obtained from the sorting of PMA-induced THP-1 cells. Similarly, ( F – H ) depict the gating strategy utilized during the sorting of THP-1 cells in the control group. ( I ) exhibits a peak map illustrating the cellular composition and distribution resulting from the sorting of THP-1 cells in the control group. Finally, ( J ) provides the percentage composition of FITC-positive cells obtained from the sorting of THP-1 cells in the control group.

    Journal: Viruses

    Article Title: Time-Course Transcriptome Analysis Reveals Distinct Phases and Identifies Two Key Genes during Severe Fever with Thrombocytopenia Syndrome Virus Infection in PMA-Induced THP-1 Cells

    doi: 10.3390/v16010059

    Figure Lengend Snippet: The results of THP-1 cell sorting using a flow cytometer with CD14-FITC labeling for cell sorting. ( A – C ) represent the gating strategy employed during the sorting of PMA-induced THP-1 cells, labeled as Gate 1 to Gate 3. ( D ) displays a peak map illustrating the cellular composition and distribution resulting from the sorting of PMA-induced THP-1 cells. ( E ) presents the percentage composition of FITC-positive cells obtained from the sorting of PMA-induced THP-1 cells. Similarly, ( F – H ) depict the gating strategy utilized during the sorting of THP-1 cells in the control group. ( I ) exhibits a peak map illustrating the cellular composition and distribution resulting from the sorting of THP-1 cells in the control group. Finally, ( J ) provides the percentage composition of FITC-positive cells obtained from the sorting of THP-1 cells in the control group.

    Article Snippet: The antibodies used in this study included Mouse Anti-Human CD14 (FITC marker) (BD) (Franklin Lakes, NJ, USA).

    Techniques: FACS, Flow Cytometry, Labeling