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preparation hl 60 cells  (ATCC)


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    ATCC preparation hl 60 cells
    Preparation Hl 60 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 6460 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/preparation+hl+60+cells/pm42104495-56-5-14?v=ATCC
    Average 99 stars, based on 6460 article reviews
    preparation hl 60 cells - by Bioz Stars, 2026-07
    99/100 stars

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    Enhancement of Raman signal of HL60 cells in HC-PCF using silver nanoparticles.

    Journal: Biomedical Optics Express

    Article Title: Hollow core photonic crystal fiber for monitoring leukemia cells using surface enhanced Raman scattering (SERS)

    doi: 10.1364/BOE.6.004599

    Figure Lengend Snippet: Enhancement of Raman signal of HL60 cells in HC-PCF using silver nanoparticles.

    Article Snippet: 2.2 Sample preparation Acute promyelocytic leukemia (HL60) cells (ATCC® CCL-240) were cultured in Iscove's Modified Dulbecco's Medium (Sigma), supplemented with 20% fetal bovine serum and 1% antibiotics (streptomycin and penicillin) and 0.1% gentamicin.

    Techniques:

    SERS spectra of different concentrations of live HL60 cells, expressed as cells/ml.

    Journal: Biomedical Optics Express

    Article Title: Hollow core photonic crystal fiber for monitoring leukemia cells using surface enhanced Raman scattering (SERS)

    doi: 10.1364/BOE.6.004599

    Figure Lengend Snippet: SERS spectra of different concentrations of live HL60 cells, expressed as cells/ml.

    Article Snippet: 2.2 Sample preparation Acute promyelocytic leukemia (HL60) cells (ATCC® CCL-240) were cultured in Iscove's Modified Dulbecco's Medium (Sigma), supplemented with 20% fetal bovine serum and 1% antibiotics (streptomycin and penicillin) and 0.1% gentamicin.

    Techniques:

    Number of events vs. total number of cells/mL for HL60 cells. Number of events was quantified by using the scattering upon 488-nm excitation of a non-stained cell suspension. Top inset shows the scattering profile for the sample containing 25,000 cells/mL. Bottom inset shows a magnification for the lower cell numbers where the red area denotes the noise region or lower limit of detection for the system. Right panels include the scattering profile for the sample with 310 cells/mL and a control solution without any cells, where it can be clearly seen the close similarity between the two plots.

    Journal: Biomedical Optics Express

    Article Title: Hollow core photonic crystal fiber for monitoring leukemia cells using surface enhanced Raman scattering (SERS)

    doi: 10.1364/BOE.6.004599

    Figure Lengend Snippet: Number of events vs. total number of cells/mL for HL60 cells. Number of events was quantified by using the scattering upon 488-nm excitation of a non-stained cell suspension. Top inset shows the scattering profile for the sample containing 25,000 cells/mL. Bottom inset shows a magnification for the lower cell numbers where the red area denotes the noise region or lower limit of detection for the system. Right panels include the scattering profile for the sample with 310 cells/mL and a control solution without any cells, where it can be clearly seen the close similarity between the two plots.

    Article Snippet: 2.2 Sample preparation Acute promyelocytic leukemia (HL60) cells (ATCC® CCL-240) were cultured in Iscove's Modified Dulbecco's Medium (Sigma), supplemented with 20% fetal bovine serum and 1% antibiotics (streptomycin and penicillin) and 0.1% gentamicin.

    Techniques: Staining, Suspension, Control