cd57 apc (Miltenyi Biotec)
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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
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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), 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), 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), |

![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.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_1300/pmc11161300/pmc11161300__bs9-6-e00194-g005.jpg)