cell lines pl21 (DSMZ)
Structured Review

Cell Lines Pl21, supplied by DSMZ, used in various techniques. Bioz Stars score: 94/100, based on 35 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/cell lines pl21/product/DSMZ
Average 94 stars, based on 35 article reviews
Images
1) Product Images from "Characterization and comparative analysis of multifunctional natural killer cell engagers during antitumor responses."
Article Title: Characterization and comparative analysis of multifunctional natural killer cell engagers during antitumor responses.
Journal: Cell reports. Medicine
doi: 10.1016/j.xcrm.2025.102117
Figure Legend Snippet: Figure 1. NKCEs redirect NK cells to kill target cells with minimal cytokine release (A) Design of tool molecules NCR1xHER2 (NKCE) and CD3xHER2 (TCE). (B) HER2 expression on JIMT1-Luc WT and HER2−/−. Antibodies bound per cell (ABCs) of HER2 are indicated in the graph. (C and D) JIMT1-Luc WT and HER2−/−were incubated with NK cells or Pan T cells at an E:T cell ratio of 5:1 and increasing concentrations of NCR1xHER2 or CD3xHER2. (C) JIMT1-Luc cell lysis at 24 h; concentrations of TNF and IFNγ (D) in the cell culture supernatants at 24 h. (E) Design of tool molecules NCR1xCLL1 (NKCE-I) and CD3xCLL1 (huCLL1 TCE). (F) CLL1 expression on PL21-Luc, NOMO1-Luc, and MOLM13-Luc. ABC of CLL1 is indicated in the graph. (G and H) PL21-Luc, NOMO1-Luc, and MOLM13-Luc were incubated with NK cells or Pan T cells at an E:T cell ratio of 2.5:1 and increasing concentrations of NKCE-I or huCLL1 TCE. (G) Target cell lysis at 48 h; (H) concentrations of TNF in the cell culture supernatants at 48 h. Data are presented as means ± SEM (C). The data shown are representative of at least two independent experiments.
Techniques Used: Expressing, Incubation, Lysis, Cell Culture
Figure Legend Snippet: Figure 3. Multiple functional NKCEs induce robust killing activity with minimal TNF production (A) Components and designs of multifunctional NKCEs: NKCE-I to NKCE-V. (B–D) NOMO1-Luc cells were incubated with NK cells or Pan T cells at an E:T cell ratio of 2.5:1 and increasing concentrations of NKCE-I to NKCE-V and IL-2 or TCE. (B) NOMO1-Luc lysis at 48 h. EC50 and area under curve (AUC) are indicated in the graph. Concentrations of TNF (C) and IFNγ (D) in the cell culture su- pernatants at 48 h. (E) CLL1 expression on PL21-Luc WT and CLL1low. ABC of CLL1 is indicated in the graph. (F–H) PL21-Luc WT or CLL1low cells were incubated with NK cells at an E:T cell ratio of 2.5:1 and increasing concentrations of NKCE-III (F), NKCE-IV (G), and NKCE-V (H) and PL21-Luc lysis at 48 h. Data are presented as means ± SEM (B). The data shown are representative of at least two independent experiments.
Techniques Used: Functional Assay, Activity Assay, Incubation, Lysis, Cell Culture, Expressing
