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cd57 apc  (Miltenyi Biotec)


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    Structured Review

    Miltenyi Biotec cd57 apc
    Cd57 Apc, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 63 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cd57+apc/CD57+Antibody%2C+anti-human/pm41307128-464-5-7
    Average 94 stars, based on 63 article reviews
    cd57 apc - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Bioprocessing:

    Article Title: Telomerase Reverse Transcriptase Increases Proliferation and Lifespan of Human NK Cells without Immortalization
    Article Snippet: .. The following mouse monoclonal antibodies were used: CD56-APC (clone N901, Beckman Coulter, Miami, FL, USA), CD56-Brilliant Violet 421 (clone HCD56, Sony Biotechnology, San Jose, CA, USA), CD56-PE (clone N901 (HLDA6), Beckman Coulter, Miami, FL, USA), CD57-PE (clone TB01, eBioscience, San Diego, CA, USA), CD57-FITC (clone TB03, Miltenyi Biotec, Bergisch Gladbach, Germany), CD57-APC (clone TB03, Miltenyi Biotec, Bergisch Gladbach, Germany), CD16-PE (Sorbent, RF), CD2-PE-Cy7 (clone TS1/8, Sony Biotechnology, San Jose, CA, USA), anti-NKG2A-PE (clone 131411, R&D Systems, Minneapolis, MN, USA), anti-KIR2DL2/DL3-PE (clone DX27, Miltenyi Biotec, Bergisch Gladbach, Germany), anti-HLA-DR-FITC (clone B8.12.2, Beckman Coulter, Miami, FL, CA, USA), NKG2A-PE (clone 131411), NKG2C-AlexaFluor488 (clone 108724), NKG2C-PE (clone 134591; R&D Systems, Minneapolis, MN, USA), NKp46-FITC (clone 9E2; Sony Biotechnology, San Jose, CA, USA), anti-NKG2D-PE (clone REA1175, Miltenyi Biotec, Bergisch Gladbach, Germany). ..

    Article Title: Analysis of NK cell clones obtained using interleukin-2 and gene-modified K562 cells revealed the ability of “senescent” NK cells to lose CD57 expression and start expressing NKG2A
    Article Snippet: Prior to use as feeder cells, К562-mbIL21 cells were irradiated with γ radiation (100 Gy) and frozen in 90% FCS containing 10% DMSO (Sigma, USA) at –150°C. .. The following anti-human monoclonal antibodies (mAbs) were used for flow cytometry: CD3- PE-Cy7 (Beckman Coulter, USA, clone UCHT1), CD56-APC (Beckman Coulter, USA, clone N901), CD56-Brilliant Violet 421 (Sony, USA, clone HCD56), CD56-PE (Beckman Coulter, USA, clone N901 (HLDA6)), CD57-PE (eBioscience, USA, clone TB01), CD57-FITC (Miltenyi Biotech, Germany, clone TB03), CD57-APC (Miltenyi Biotech, Germany, TB03), CD16-PE (Sony, USA) anti-NKG2A-PE (R&D Systems, USA, clone 131411), anti-KIR2DL2/DL3-PE (Miltenyi Biotech, Germany, clone DX27), anti-HLA-DR-FITC (Beckman Coulter, USA, clone B8.12.2). ..

    Flow Cytometry:

    Article Title: Analysis of NK cell clones obtained using interleukin-2 and gene-modified K562 cells revealed the ability of “senescent” NK cells to lose CD57 expression and start expressing NKG2A
    Article Snippet: Prior to use as feeder cells, К562-mbIL21 cells were irradiated with γ radiation (100 Gy) and frozen in 90% FCS containing 10% DMSO (Sigma, USA) at –150°C. .. The following anti-human monoclonal antibodies (mAbs) were used for flow cytometry: CD3- PE-Cy7 (Beckman Coulter, USA, clone UCHT1), CD56-APC (Beckman Coulter, USA, clone N901), CD56-Brilliant Violet 421 (Sony, USA, clone HCD56), CD56-PE (Beckman Coulter, USA, clone N901 (HLDA6)), CD57-PE (eBioscience, USA, clone TB01), CD57-FITC (Miltenyi Biotech, Germany, clone TB03), CD57-APC (Miltenyi Biotech, Germany, TB03), CD16-PE (Sony, USA) anti-NKG2A-PE (R&D Systems, USA, clone 131411), anti-KIR2DL2/DL3-PE (Miltenyi Biotech, Germany, clone DX27), anti-HLA-DR-FITC (Beckman Coulter, USA, clone B8.12.2). ..



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    Frequency of CD27, CD28, and <t>CD57</t> expression on the bone marrow CD8 + TRM-like subset of HIs and patients with ND-AML. (A–C) Flow cytometry was used to detect the distribution and frequency of CD27 (A), CD28 (B), and CD57 (C) on the CD69 − TEM and CD8 + TRM-like cell subsets in the BM of HIs and patients with ND-AML. Compared with CD69 − TEM, the CD8 + TRM-like subset expressed CD27 and CD28 and low expression of CD57. The number (n) of samples included in each subset analysis is shown as follows, HI (n [CD27 + ] = 17, n [CD28 + ] = 14, n [CD57 + ] = 18), AML (n [CD27 + ] = 41, n [CD28 + ] = 32, n [CD57 + ] = 47). Wilcoxon test and paired t test were used for paired sample analysis. AML = acute myeloid leukemia, HI = healthy individual, ND = newly diagnosed, ns = not significant, TEM = effector memory T cell, TRM-like = tissue-resident-like T cell.
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    Image Search Results


    Antibody panel.

    Journal: Frontiers in Immunology

    Article Title: Good manufacturing practice-grade generation of CD19 and CD123-specific CAR-T cells using piggyBac transposon and allogeneic feeder cells in patients diagnosed with B-cell non-Hodgkin lymphoma and acute myeloid leukemia

    doi: 10.3389/fimmu.2024.1415328

    Figure Lengend Snippet: Antibody panel.

    Article Snippet: CD57 , APC-Vio770 , REA769 , Miltenyi Biotec , 130–111-813.

    Techniques: Staining

    Frequency of CD27, CD28, and CD57 expression on the bone marrow CD8 + TRM-like subset of HIs and patients with ND-AML. (A–C) Flow cytometry was used to detect the distribution and frequency of CD27 (A), CD28 (B), and CD57 (C) on the CD69 − TEM and CD8 + TRM-like cell subsets in the BM of HIs and patients with ND-AML. Compared with CD69 − TEM, the CD8 + TRM-like subset expressed CD27 and CD28 and low expression of CD57. The number (n) of samples included in each subset analysis is shown as follows, HI (n [CD27 + ] = 17, n [CD28 + ] = 14, n [CD57 + ] = 18), AML (n [CD27 + ] = 41, n [CD28 + ] = 32, n [CD57 + ] = 47). Wilcoxon test and paired t test were used for paired sample analysis. AML = acute myeloid leukemia, HI = healthy individual, ND = newly diagnosed, ns = not significant, TEM = effector memory T cell, TRM-like = tissue-resident-like T cell.

    Journal: Blood Science

    Article Title: High percentage of bone marrow CD8 + tissue-resident-like memory T cells predicts inferior survival in patients with acute myeloid leukemia

    doi: 10.1097/BS9.0000000000000194

    Figure Lengend Snippet: Frequency of CD27, CD28, and CD57 expression on the bone marrow CD8 + TRM-like subset of HIs and patients with ND-AML. (A–C) Flow cytometry was used to detect the distribution and frequency of CD27 (A), CD28 (B), and CD57 (C) on the CD69 − TEM and CD8 + TRM-like cell subsets in the BM of HIs and patients with ND-AML. Compared with CD69 − TEM, the CD8 + TRM-like subset expressed CD27 and CD28 and low expression of CD57. The number (n) of samples included in each subset analysis is shown as follows, HI (n [CD27 + ] = 17, n [CD28 + ] = 14, n [CD57 + ] = 18), AML (n [CD27 + ] = 41, n [CD28 + ] = 32, n [CD57 + ] = 47). Wilcoxon test and paired t test were used for paired sample analysis. AML = acute myeloid leukemia, HI = healthy individual, ND = newly diagnosed, ns = not significant, TEM = effector memory T cell, TRM-like = tissue-resident-like T cell.

    Article Snippet: Cell surface staining for flow cytometry was performed using the following antibodies: CD45-BU395 (clone HI30; BD, San Jose, California), CD3-AF700 (clone UCHT1, BD), CD8-APC-H7 (clone SK1, BD), CD4-APC-H7 (clone RPA-T4, BD), CCR7-BV605 (clone 3D12, BD), CD45RA-BV510 (clone HI100, BD), CD69-PerCP-Cy5.5 (clone FN50, BD), CD69-PE-Cy7 (clone FN50, BD), PD1-BV421 (clone MIH4, BD), TIGIT-PE (clone A15153G; BioLegend, San Diego, California), CD226-PE-Cy7 (clone 11A8; BioLegend), CD27-PE (clone O323; BioLegend), CD28-PerCP-Cy5.5 (clone CD28.2; BioLegend), and CD57-APC (clone NK-1; BD).

    Techniques: Expressing, Flow Cytometry