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apc anti human cd8a antibody  (Elabscience Biotechnology)


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    Structured Review

    Elabscience Biotechnology apc anti human cd8a antibody
    Immune cell infiltration in KRAS G12C mutant PNETs (A) Quantitative analysis using Image Plus 6.0 software reveals a significant increase in Tregs (CD4 + , CD25 + , and FoxP3 + ) within KRAS- G12C mutant PNETs compared to wild-type KRAS PNET tissues, suggesting KRAS G12C -driven immunosuppressive cell recruitment. (B) Fluorescence intensity analysis demonstrates reduced infiltration of <t>CD8</t> + cytotoxic T cells and HLA-DR + activated cells in KRAS G12C mutant tumors, indicative of impaired antitumor immunity. (C) Elevated MDSCs counts in KRAS G12C mutant PNETs correlate with enhanced immune evasion.
    Apc Anti Human Cd8a Antibody, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Hypoxic-immune axis orchestrates metastatic dissemination via HIF isoform imbalance in pancreatic neuroendocrine tumors"

    Article Title: Hypoxic-immune axis orchestrates metastatic dissemination via HIF isoform imbalance in pancreatic neuroendocrine tumors

    Journal: iScience

    doi: 10.1016/j.isci.2025.114340

    Immune cell infiltration in KRAS G12C mutant PNETs (A) Quantitative analysis using Image Plus 6.0 software reveals a significant increase in Tregs (CD4 + , CD25 + , and FoxP3 + ) within KRAS- G12C mutant PNETs compared to wild-type KRAS PNET tissues, suggesting KRAS G12C -driven immunosuppressive cell recruitment. (B) Fluorescence intensity analysis demonstrates reduced infiltration of CD8 + cytotoxic T cells and HLA-DR + activated cells in KRAS G12C mutant tumors, indicative of impaired antitumor immunity. (C) Elevated MDSCs counts in KRAS G12C mutant PNETs correlate with enhanced immune evasion.
    Figure Legend Snippet: Immune cell infiltration in KRAS G12C mutant PNETs (A) Quantitative analysis using Image Plus 6.0 software reveals a significant increase in Tregs (CD4 + , CD25 + , and FoxP3 + ) within KRAS- G12C mutant PNETs compared to wild-type KRAS PNET tissues, suggesting KRAS G12C -driven immunosuppressive cell recruitment. (B) Fluorescence intensity analysis demonstrates reduced infiltration of CD8 + cytotoxic T cells and HLA-DR + activated cells in KRAS G12C mutant tumors, indicative of impaired antitumor immunity. (C) Elevated MDSCs counts in KRAS G12C mutant PNETs correlate with enhanced immune evasion.

    Techniques Used: Mutagenesis, Software, Fluorescence

    Tregs, CD8 + T cells, and HLA-DR + cells in KRAS G12C -mutated PNETs (A) Flow cytometry plots and fluorescence intensity histograms demonstrate elevated CD4 + T cell proportions in KRAS G12C patient blood samples compared to wild-type KRAS tumors and healthy controls. (B) Quantification shows a significant enrichment of CD25 + T cells in KRAS G12C patients, surpassing both wild-type KRAS tumors and normal controls. (C) Quantitative data and histogram overlays confirm a substantial increase in FoxP3 + T cells frequency in KRAS G12C patients, with levels moderately elevated compared to wild-type KRAS and significantly higher than healthy individuals. (D) A slight decrease in CD8 + T cell frequency in KRAS G12C samples relative to wild-type KRAS, with levels significantly lower than those in healthy individuals (E) A moderate reduction in HLA-DR + cell frequency in KRAS G12C patients compared to wild-type KRAS, alongside a marked suppression relative to healthy controls.
    Figure Legend Snippet: Tregs, CD8 + T cells, and HLA-DR + cells in KRAS G12C -mutated PNETs (A) Flow cytometry plots and fluorescence intensity histograms demonstrate elevated CD4 + T cell proportions in KRAS G12C patient blood samples compared to wild-type KRAS tumors and healthy controls. (B) Quantification shows a significant enrichment of CD25 + T cells in KRAS G12C patients, surpassing both wild-type KRAS tumors and normal controls. (C) Quantitative data and histogram overlays confirm a substantial increase in FoxP3 + T cells frequency in KRAS G12C patients, with levels moderately elevated compared to wild-type KRAS and significantly higher than healthy individuals. (D) A slight decrease in CD8 + T cell frequency in KRAS G12C samples relative to wild-type KRAS, with levels significantly lower than those in healthy individuals (E) A moderate reduction in HLA-DR + cell frequency in KRAS G12C patients compared to wild-type KRAS, alongside a marked suppression relative to healthy controls.

    Techniques Used: Flow Cytometry, Fluorescence



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    Immune cell infiltration in KRAS G12C mutant PNETs (A) Quantitative analysis using Image Plus 6.0 software reveals a significant increase in Tregs (CD4 + , CD25 + , and FoxP3 + ) within KRAS- G12C mutant PNETs compared to wild-type KRAS PNET tissues, suggesting KRAS G12C -driven immunosuppressive cell recruitment. (B) Fluorescence intensity analysis demonstrates reduced infiltration of <t>CD8</t> + cytotoxic T cells and HLA-DR + activated cells in KRAS G12C mutant tumors, indicative of impaired antitumor immunity. (C) Elevated MDSCs counts in KRAS G12C mutant PNETs correlate with enhanced immune evasion.
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    Immune cell infiltration in KRAS G12C mutant PNETs (A) Quantitative analysis using Image Plus 6.0 software reveals a significant increase in Tregs (CD4 + , CD25 + , and FoxP3 + ) within KRAS- G12C mutant PNETs compared to wild-type KRAS PNET tissues, suggesting KRAS G12C -driven immunosuppressive cell recruitment. (B) Fluorescence intensity analysis demonstrates reduced infiltration of <t>CD8</t> + cytotoxic T cells and HLA-DR + activated cells in KRAS G12C mutant tumors, indicative of impaired antitumor immunity. (C) Elevated MDSCs counts in KRAS G12C mutant PNETs correlate with enhanced immune evasion.
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    Image Search Results


    Immune cell infiltration in KRAS G12C mutant PNETs (A) Quantitative analysis using Image Plus 6.0 software reveals a significant increase in Tregs (CD4 + , CD25 + , and FoxP3 + ) within KRAS- G12C mutant PNETs compared to wild-type KRAS PNET tissues, suggesting KRAS G12C -driven immunosuppressive cell recruitment. (B) Fluorescence intensity analysis demonstrates reduced infiltration of CD8 + cytotoxic T cells and HLA-DR + activated cells in KRAS G12C mutant tumors, indicative of impaired antitumor immunity. (C) Elevated MDSCs counts in KRAS G12C mutant PNETs correlate with enhanced immune evasion.

    Journal: iScience

    Article Title: Hypoxic-immune axis orchestrates metastatic dissemination via HIF isoform imbalance in pancreatic neuroendocrine tumors

    doi: 10.1016/j.isci.2025.114340

    Figure Lengend Snippet: Immune cell infiltration in KRAS G12C mutant PNETs (A) Quantitative analysis using Image Plus 6.0 software reveals a significant increase in Tregs (CD4 + , CD25 + , and FoxP3 + ) within KRAS- G12C mutant PNETs compared to wild-type KRAS PNET tissues, suggesting KRAS G12C -driven immunosuppressive cell recruitment. (B) Fluorescence intensity analysis demonstrates reduced infiltration of CD8 + cytotoxic T cells and HLA-DR + activated cells in KRAS G12C mutant tumors, indicative of impaired antitumor immunity. (C) Elevated MDSCs counts in KRAS G12C mutant PNETs correlate with enhanced immune evasion.

    Article Snippet: APC Anti-Human CD8a Antibody [OKT-8] , Elabscience , E-AB-F1110E.

    Techniques: Mutagenesis, Software, Fluorescence

    Tregs, CD8 + T cells, and HLA-DR + cells in KRAS G12C -mutated PNETs (A) Flow cytometry plots and fluorescence intensity histograms demonstrate elevated CD4 + T cell proportions in KRAS G12C patient blood samples compared to wild-type KRAS tumors and healthy controls. (B) Quantification shows a significant enrichment of CD25 + T cells in KRAS G12C patients, surpassing both wild-type KRAS tumors and normal controls. (C) Quantitative data and histogram overlays confirm a substantial increase in FoxP3 + T cells frequency in KRAS G12C patients, with levels moderately elevated compared to wild-type KRAS and significantly higher than healthy individuals. (D) A slight decrease in CD8 + T cell frequency in KRAS G12C samples relative to wild-type KRAS, with levels significantly lower than those in healthy individuals (E) A moderate reduction in HLA-DR + cell frequency in KRAS G12C patients compared to wild-type KRAS, alongside a marked suppression relative to healthy controls.

    Journal: iScience

    Article Title: Hypoxic-immune axis orchestrates metastatic dissemination via HIF isoform imbalance in pancreatic neuroendocrine tumors

    doi: 10.1016/j.isci.2025.114340

    Figure Lengend Snippet: Tregs, CD8 + T cells, and HLA-DR + cells in KRAS G12C -mutated PNETs (A) Flow cytometry plots and fluorescence intensity histograms demonstrate elevated CD4 + T cell proportions in KRAS G12C patient blood samples compared to wild-type KRAS tumors and healthy controls. (B) Quantification shows a significant enrichment of CD25 + T cells in KRAS G12C patients, surpassing both wild-type KRAS tumors and normal controls. (C) Quantitative data and histogram overlays confirm a substantial increase in FoxP3 + T cells frequency in KRAS G12C patients, with levels moderately elevated compared to wild-type KRAS and significantly higher than healthy individuals. (D) A slight decrease in CD8 + T cell frequency in KRAS G12C samples relative to wild-type KRAS, with levels significantly lower than those in healthy individuals (E) A moderate reduction in HLA-DR + cell frequency in KRAS G12C patients compared to wild-type KRAS, alongside a marked suppression relative to healthy controls.

    Article Snippet: APC Anti-Human CD8a Antibody [OKT-8] , Elabscience , E-AB-F1110E.

    Techniques: Flow Cytometry, Fluorescence

    a HST-NEET products ( n = 6) exhibited variable antigen-specific IFN-γ responses against HIV Gag, Pol, Nef, and conserved epitope targets in the Gag/Pol Mos1 and Mos2 peptide mixes. RESIST-004 HST-NEET numbers after treatment-related studies were insufficient to test Gag/Pol Mos1 and Mos2 specificity. Positive ELISpot results were defined as IFN-γ spot forming cells ≥2 times the actin negative control. Spot forming cells (SFC) per 10 5 cells indicative of specific responses compared to actin stimulated cells: RESIST-001 (actin [17 SFC], nef [139 SFC]), RESIST-003 (actin [19 SFC], gag [659 SFC], pol [466 SFC], nef [1057 SFC], mos1 [540 SFC], mos2 [520 SFC]), RESIST-004 (actin [34 SFC], nef [117 SFC]), RESIST-005 (actin [65 SFC], nef [804 SFC]), RESIST-006 (actin [0 SFC], nef [236 SFC]), and RESIST-007 (actin [25 SFC], gag [1063 SFC], nef [854 SFC], mos1 [291 SFC], mos2 [290 SFC]). b Each bar reports the total sum (infusion 1 and infusion 2) of infused T cells specific for HIV Gag, Pol, and Nef epitopes for each HST-NEETs product ( n = 5). c Each bar reports the total sum (infusion 1 and infusion 2) of infused T cells specific for conserved epitopes in Gag/Pol Mosaic 1 and Mosaic 2 immunogens for each HST-NEETs product ( n = 5). d , e HST-NEET products ( n = 6) were predominantly CD8+ effector memory T cells and had variable expression of T cell surface activation and exhaustion markers. f CD3+ CD8+ HST-NEET products ( n = 5) exhibited polyfunctional T cell responses upon stimulation with Gag, Pol, Nef and Gag/Pol Mos1 and Mos2 peptides as measured by intracellular production of IFN-γ and TNF-α. HIV-specific T cell activation was dominant in the CD8+ T cell fraction of all HST-NEET products. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Autologous HIV-specific T cell therapy targeting conserved epitopes is well-tolerated in six adults with HIV: an open-label, single-arm phase 1 study

    doi: 10.1038/s41467-025-59810-2

    Figure Lengend Snippet: a HST-NEET products ( n = 6) exhibited variable antigen-specific IFN-γ responses against HIV Gag, Pol, Nef, and conserved epitope targets in the Gag/Pol Mos1 and Mos2 peptide mixes. RESIST-004 HST-NEET numbers after treatment-related studies were insufficient to test Gag/Pol Mos1 and Mos2 specificity. Positive ELISpot results were defined as IFN-γ spot forming cells ≥2 times the actin negative control. Spot forming cells (SFC) per 10 5 cells indicative of specific responses compared to actin stimulated cells: RESIST-001 (actin [17 SFC], nef [139 SFC]), RESIST-003 (actin [19 SFC], gag [659 SFC], pol [466 SFC], nef [1057 SFC], mos1 [540 SFC], mos2 [520 SFC]), RESIST-004 (actin [34 SFC], nef [117 SFC]), RESIST-005 (actin [65 SFC], nef [804 SFC]), RESIST-006 (actin [0 SFC], nef [236 SFC]), and RESIST-007 (actin [25 SFC], gag [1063 SFC], nef [854 SFC], mos1 [291 SFC], mos2 [290 SFC]). b Each bar reports the total sum (infusion 1 and infusion 2) of infused T cells specific for HIV Gag, Pol, and Nef epitopes for each HST-NEETs product ( n = 5). c Each bar reports the total sum (infusion 1 and infusion 2) of infused T cells specific for conserved epitopes in Gag/Pol Mosaic 1 and Mosaic 2 immunogens for each HST-NEETs product ( n = 5). d , e HST-NEET products ( n = 6) were predominantly CD8+ effector memory T cells and had variable expression of T cell surface activation and exhaustion markers. f CD3+ CD8+ HST-NEET products ( n = 5) exhibited polyfunctional T cell responses upon stimulation with Gag, Pol, Nef and Gag/Pol Mos1 and Mos2 peptides as measured by intracellular production of IFN-γ and TNF-α. HIV-specific T cell activation was dominant in the CD8+ T cell fraction of all HST-NEET products. Source data are provided as a Source Data file.

    Article Snippet: Antibodies used in panels for cell surface staining differed between the GMP and non-GMP laboratories, and were combinations of the following: CD3 PE-Cy7 (Cat: 317334, Biolegend), CD3 PerCP-Vio700 (Cat: 130-113-141, Miltenyi), CD3 BV785 (Cat: 317330, Biolegend), CD4 BV605 (Cat: 317438, Biolegend), CD4 PE Vio770 (Cat: 130-113-227, Miltenyi), CD8a BV421 (Cat: 301036, Biolegend), CD8a APC Vio770 (Cat: 130-110-681, Miltenyi), CCR7 Alexa Fluor 700 (Cat: 353244, Biolegend), CCR7 FITC (Cat: 130-120-468, Miltenyi), CD45RO PE-Dazzle 594 (Cat: 304248, Biolegend), CD45RO PE (Cat: 130-113-559, Miltenyi), CD19 FITC (Cat: 130-113-645, Miltenyi), CD14 VioBlue (Cat: 130-110-524, Miltenyi), CD16 PE (Cat: 130-113-393, Miltenyi), CD56 BV650 (Cat: 318344, Biolegend), CD56 PE (Cat: 130-113-312, Miltenyi), TCRγδ APC-Fire 750 (Cat: 331228, Biolegend), TCRγδ (Cat: 130-113-512, Miltenyi), TCRαβ PerCP/Cyanine5.5 (Cat: 306724, Biolegend), TCRαβ FITC (Cat: 130-113-538, Miltenyi), CD160 PE-Cy7 (Cat: 341212, Biolegend), CTLA4 PE-Dazzle 594 (Cat: 369616, Biolegend), LAG3 PE (Cat: 369306, Biolegend), PD-1 FITC (Cat: 329904, Biolegend), TIM3 BV650 (Cat: 345028, Biolegend), CD107a PE-Cy7 (Cat: 328618, Biolegend), CD45 APC (Cat: 130-110-633, Miltenyi), CD83 PE (Cat: 130-110-503, Miltenyi), CD62 VioBlue (Cat: 130-113-622, Miltenyi), HLA-DR FITC (Cat: 30-111-788, Miltenyi), and CD95 APC (Cat: 558814, BD Biosciences).

    Techniques: Enzyme-linked Immunospot, Negative Control, Expressing, Activation Assay

    a Comprehensive pooled peptide epitope mapping of HST-NEETs revealed 15-mer peptides driving HIV-specific responses in each product ( n = 5). RESIST-001, -003, -005, and -006 ELISpots were conducted as singlets based on HST-NEET numbers available for characterization studies, and RESIST-007 ELISpots were conducted in duplicate. Plotted SFC per 10 5 cells is shown above each bar. b – f HST-NEET products were stimulated with 15-mer peptides in ( a ) for 5 h and intracellular production of IFN-γ and TNF-α in CD8+ T cells was evaluated to confirm epitope-specific responses. Peptides evaluated are named by the first two amino acids in the 15-mer sequence followed by the peptide length. g Minimal (9 amino acid) epitopes associated with CD8+ T cell responses were determined for each product. RESIST-004 HST-NEETs were unavailable for these product characterization studies. Positive ELISpot results were defined as IFN-γ spot forming cells ≥2 times the actin negative control. RESIST-005 ELISpots were conducted as singlets, RESIST-001, -003, -006, and -007 were conducted in duplicate. Plotted SFC per 10 5 cells is shown above each bar.

    Journal: Nature Communications

    Article Title: Autologous HIV-specific T cell therapy targeting conserved epitopes is well-tolerated in six adults with HIV: an open-label, single-arm phase 1 study

    doi: 10.1038/s41467-025-59810-2

    Figure Lengend Snippet: a Comprehensive pooled peptide epitope mapping of HST-NEETs revealed 15-mer peptides driving HIV-specific responses in each product ( n = 5). RESIST-001, -003, -005, and -006 ELISpots were conducted as singlets based on HST-NEET numbers available for characterization studies, and RESIST-007 ELISpots were conducted in duplicate. Plotted SFC per 10 5 cells is shown above each bar. b – f HST-NEET products were stimulated with 15-mer peptides in ( a ) for 5 h and intracellular production of IFN-γ and TNF-α in CD8+ T cells was evaluated to confirm epitope-specific responses. Peptides evaluated are named by the first two amino acids in the 15-mer sequence followed by the peptide length. g Minimal (9 amino acid) epitopes associated with CD8+ T cell responses were determined for each product. RESIST-004 HST-NEETs were unavailable for these product characterization studies. Positive ELISpot results were defined as IFN-γ spot forming cells ≥2 times the actin negative control. RESIST-005 ELISpots were conducted as singlets, RESIST-001, -003, -006, and -007 were conducted in duplicate. Plotted SFC per 10 5 cells is shown above each bar.

    Article Snippet: Antibodies used in panels for cell surface staining differed between the GMP and non-GMP laboratories, and were combinations of the following: CD3 PE-Cy7 (Cat: 317334, Biolegend), CD3 PerCP-Vio700 (Cat: 130-113-141, Miltenyi), CD3 BV785 (Cat: 317330, Biolegend), CD4 BV605 (Cat: 317438, Biolegend), CD4 PE Vio770 (Cat: 130-113-227, Miltenyi), CD8a BV421 (Cat: 301036, Biolegend), CD8a APC Vio770 (Cat: 130-110-681, Miltenyi), CCR7 Alexa Fluor 700 (Cat: 353244, Biolegend), CCR7 FITC (Cat: 130-120-468, Miltenyi), CD45RO PE-Dazzle 594 (Cat: 304248, Biolegend), CD45RO PE (Cat: 130-113-559, Miltenyi), CD19 FITC (Cat: 130-113-645, Miltenyi), CD14 VioBlue (Cat: 130-110-524, Miltenyi), CD16 PE (Cat: 130-113-393, Miltenyi), CD56 BV650 (Cat: 318344, Biolegend), CD56 PE (Cat: 130-113-312, Miltenyi), TCRγδ APC-Fire 750 (Cat: 331228, Biolegend), TCRγδ (Cat: 130-113-512, Miltenyi), TCRαβ PerCP/Cyanine5.5 (Cat: 306724, Biolegend), TCRαβ FITC (Cat: 130-113-538, Miltenyi), CD160 PE-Cy7 (Cat: 341212, Biolegend), CTLA4 PE-Dazzle 594 (Cat: 369616, Biolegend), LAG3 PE (Cat: 369306, Biolegend), PD-1 FITC (Cat: 329904, Biolegend), TIM3 BV650 (Cat: 345028, Biolegend), CD107a PE-Cy7 (Cat: 328618, Biolegend), CD45 APC (Cat: 130-110-633, Miltenyi), CD83 PE (Cat: 130-110-503, Miltenyi), CD62 VioBlue (Cat: 130-113-622, Miltenyi), HLA-DR FITC (Cat: 30-111-788, Miltenyi), and CD95 APC (Cat: 558814, BD Biosciences).

    Techniques: Sequencing, Enzyme-linked Immunospot, Negative Control