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diff-quik staining method  (Siemens Healthineers)

 
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    Siemens Healthineers diff-quik staining method
    Diff Quik Staining Method, supplied by Siemens Healthineers, 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/product/diff-quik+stained+method/diff+quik+stain+set/pm29198956-44-2-5
    Average 90 stars, based on 1 article reviews
    diff-quik staining method - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Sterility:

    Article Title: Metabolic regulation of the dog ovary: Immunofluorescent characterization of PPARs from prepubertal development to the estrous cycle.
    Article Snippet: The dog ovary undergoes dynamic and metabolic remodeling during prepubertal development and throughout the estrous cycle.. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated nuclear transcription factors that regulate lipid metabolism and cellular differentiation; however, their stage-specific spatial regulation in the dog ovary remains poorly defined.. This study characterized the compartment-specific localization and semi-quantitative abundance patterns of PPARα, PPARδ, and PPARγ in prepubertal and cyclic sexually mature dogs.

    Staining:

    Article Title: Metabolic regulation of the dog ovary: Immunofluorescent characterization of PPARs from prepubertal development to the estrous cycle.
    Article Snippet: The dog ovary undergoes dynamic and metabolic remodeling during prepubertal development and throughout the estrous cycle.. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated nuclear transcription factors that regulate lipid metabolism and cellular differentiation; however, their stage-specific spatial regulation in the dog ovary remains poorly defined.. This study characterized the compartment-specific localization and semi-quantitative abundance patterns of PPARα, PPARδ, and PPARγ in prepubertal and cyclic sexually mature dogs.

    Diff-Quik:

    Article Title: Metabolic regulation of the dog ovary: Immunofluorescent characterization of PPARs from prepubertal development to the estrous cycle.
    Article Snippet: The dog ovary undergoes dynamic and metabolic remodeling during prepubertal development and throughout the estrous cycle.. Peroxisome proliferator-activated receptors (PPARs) are ligand-activated nuclear transcription factors that regulate lipid metabolism and cellular differentiation; however, their stage-specific spatial regulation in the dog ovary remains poorly defined.. This study characterized the compartment-specific localization and semi-quantitative abundance patterns of PPARα, PPARδ, and PPARγ in prepubertal and cyclic sexually mature dogs.

    other:

    Article Title: Familial adenomatous polyposis-associated, cribriform morular variant of papillary thyroid carcinoma harboring a K-RAS mutation: case presentation and review of molecular mechanisms.
    Article Snippet: Background: The cribriform morular variant of papillary thyroid carcinoma (CMVPTC) is a rare subtype of papillary thyroid cancer that occurs most often in association with the familial adenomatous polyposis (FAP) syndrome.. Patient findings: A 18-year-old woman presented with recurrence of PTC in her neck.. She had a prior diagnosis of FAP syndrome.

    Article Title: Mouse-adapted MERS coronavirus causes lethal lung disease in human DPP4 knockin mice
    Article Snippet: Blood smears were produced using the traditional manual method, allowed to dry, and stained with Diff-Quik (Siemens Healthcare Diagnostics) or with modified Wright’s stain.



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    Inflammatory cell counts in nasal and bronchoalveolar lavage fluids (NALF and BALF) following single or combined exposure to PM2.5, Zn, and formaldehyde in a murine model of allergic rhinitis. (A) Total and differential cell counts, including eosinophils, neutrophils, lymphocytes, and monocytes, were measured in NALF from non-sensitized mice after single intranasal exposure to PM2.5, Zn, or formaldehyde. (B) Total and differential cell counts were assessed in BALF from the same non-sensitized mice following identical single exposures. (C) In ovalbumin (OVA)-sensitized mice, total and differential cell counts in NALF were evaluated after additional intranasal exposure to PM2.5 alone or in combination with Zn or formaldehyde. (D) Total and differential cell counts in BALF were measured in the same OVA-sensitized mice after combined exposures. Inflammatory cells were identified based on morphological characteristics <t>using</t> <t>Diff-Quik</t> staining. Values are presented as mean±standard deviation. NS, not significant. Statistical analysis was conducted with one-way analysis of variance followed by Tukey’s post hoc test. * P <0.05, ** P <0.01, *** P <0.001 vs. OVA or OVA+PM2.5, as indicated.
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    Inflammatory cell counts in nasal and bronchoalveolar lavage fluids (NALF and BALF) following single or combined exposure to PM2.5, Zn, and formaldehyde in a murine model of allergic rhinitis. (A) Total and differential cell counts, including eosinophils, neutrophils, lymphocytes, and monocytes, were measured in NALF from non-sensitized mice after single intranasal exposure to PM2.5, Zn, or formaldehyde. (B) Total and differential cell counts were assessed in BALF from the same non-sensitized mice following identical single exposures. (C) In ovalbumin (OVA)-sensitized mice, total and differential cell counts in NALF were evaluated after additional intranasal exposure to PM2.5 alone or in combination with Zn or formaldehyde. (D) Total and differential cell counts in BALF were measured in the same OVA-sensitized mice after combined exposures. Inflammatory cells were identified based on morphological characteristics <t>using</t> <t>Diff-Quik</t> staining. Values are presented as mean±standard deviation. NS, not significant. Statistical analysis was conducted with one-way analysis of variance followed by Tukey’s post hoc test. * P <0.05, ** P <0.01, *** P <0.001 vs. OVA or OVA+PM2.5, as indicated.
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    Inflammatory cell counts in nasal and bronchoalveolar lavage fluids (NALF and BALF) following single or combined exposure to PM2.5, Zn, and formaldehyde in a murine model of allergic rhinitis. (A) Total and differential cell counts, including eosinophils, neutrophils, lymphocytes, and monocytes, were measured in NALF from non-sensitized mice after single intranasal exposure to PM2.5, Zn, or formaldehyde. (B) Total and differential cell counts were assessed in BALF from the same non-sensitized mice following identical single exposures. (C) In ovalbumin (OVA)-sensitized mice, total and differential cell counts in NALF were evaluated after additional intranasal exposure to PM2.5 alone or in combination with Zn or formaldehyde. (D) Total and differential cell counts in BALF were measured in the same OVA-sensitized mice after combined exposures. Inflammatory cells were identified based on morphological characteristics <t>using</t> <t>Diff-Quik</t> staining. Values are presented as mean±standard deviation. NS, not significant. Statistical analysis was conducted with one-way analysis of variance followed by Tukey’s post hoc test. * P <0.05, ** P <0.01, *** P <0.001 vs. OVA or OVA+PM2.5, as indicated.
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    Image Search Results


    Inflammatory cell counts in nasal and bronchoalveolar lavage fluids (NALF and BALF) following single or combined exposure to PM2.5, Zn, and formaldehyde in a murine model of allergic rhinitis. (A) Total and differential cell counts, including eosinophils, neutrophils, lymphocytes, and monocytes, were measured in NALF from non-sensitized mice after single intranasal exposure to PM2.5, Zn, or formaldehyde. (B) Total and differential cell counts were assessed in BALF from the same non-sensitized mice following identical single exposures. (C) In ovalbumin (OVA)-sensitized mice, total and differential cell counts in NALF were evaluated after additional intranasal exposure to PM2.5 alone or in combination with Zn or formaldehyde. (D) Total and differential cell counts in BALF were measured in the same OVA-sensitized mice after combined exposures. Inflammatory cells were identified based on morphological characteristics using Diff-Quik staining. Values are presented as mean±standard deviation. NS, not significant. Statistical analysis was conducted with one-way analysis of variance followed by Tukey’s post hoc test. * P <0.05, ** P <0.01, *** P <0.001 vs. OVA or OVA+PM2.5, as indicated.

    Journal: Clinical and Experimental Otorhinolaryngology

    Article Title: Synergistic Exacerbation of Allergic Inflammation by Combined Exposure to Air-Pollutants in a Murine Model of Allergic Rhinitis

    doi: 10.21053/ceo.2025-00170

    Figure Lengend Snippet: Inflammatory cell counts in nasal and bronchoalveolar lavage fluids (NALF and BALF) following single or combined exposure to PM2.5, Zn, and formaldehyde in a murine model of allergic rhinitis. (A) Total and differential cell counts, including eosinophils, neutrophils, lymphocytes, and monocytes, were measured in NALF from non-sensitized mice after single intranasal exposure to PM2.5, Zn, or formaldehyde. (B) Total and differential cell counts were assessed in BALF from the same non-sensitized mice following identical single exposures. (C) In ovalbumin (OVA)-sensitized mice, total and differential cell counts in NALF were evaluated after additional intranasal exposure to PM2.5 alone or in combination with Zn or formaldehyde. (D) Total and differential cell counts in BALF were measured in the same OVA-sensitized mice after combined exposures. Inflammatory cells were identified based on morphological characteristics using Diff-Quik staining. Values are presented as mean±standard deviation. NS, not significant. Statistical analysis was conducted with one-way analysis of variance followed by Tukey’s post hoc test. * P <0.05, ** P <0.01, *** P <0.001 vs. OVA or OVA+PM2.5, as indicated.

    Article Snippet: Slides were stained using the Diff-Quik staining method (Sysmex).

    Techniques: Diff-Quik, Staining, Standard Deviation