mouse anti his antibody Search Results


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SouthernBiotech anti his tag mouse monoclonal antibody
Anti His Tag Mouse Monoclonal Antibody, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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OriGene mouse anti his antibody
Mouse Anti His Antibody, supplied by OriGene, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SouthernBiotech hrp conjugated mouse
a , Schematic illustration of the two OVA fusion constructs, LA-OVA (top) and the control mutLA-OVA (bottom). b , Western blot analysis of lysates from transfected and untransfected HeLa cells probed with <t>anti-His</t> (top), anti-OVA (middle) and anti-β-actin (bottom) mAbs. c , Confocal analysis of HeLa cells expressing LA-OVA (left figure, top panels) or mutLA-OVA (left figure, bottom panels). Intensity profiles for OVA (AF647) and phalloidin (AF488) channels across 10 μm (white line indicated in the confocal images) are shown on the right. Scale bars shown in confocal images (left) correspond to a size of 5μm. d - e , Flow cytometry analysis of untransfected and transfected HeLa cells before (live) and after UV treatment (UV). Overlay histograms represent intracellular staining for OVA ( d , top panels) and e ). RFP fluorescence is shown for LA-OVA and mutLA-OVA cells ( d , bottom panels). Numbers in the histogram overlay represent mean fluorescence intensity. Data are representative of 3 independent experiments.
Hrp Conjugated Mouse, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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SouthernBiotech anti his tag cat
a , Schematic illustration of the two OVA fusion constructs, LA-OVA (top) and the control mutLA-OVA (bottom). b , Western blot analysis of lysates from transfected and untransfected HeLa cells probed with <t>anti-His</t> (top), anti-OVA (middle) and anti-β-actin (bottom) mAbs. c , Confocal analysis of HeLa cells expressing LA-OVA (left figure, top panels) or mutLA-OVA (left figure, bottom panels). Intensity profiles for OVA (AF647) and phalloidin (AF488) channels across 10 μm (white line indicated in the confocal images) are shown on the right. Scale bars shown in confocal images (left) correspond to a size of 5μm. d - e , Flow cytometry analysis of untransfected and transfected HeLa cells before (live) and after UV treatment (UV). Overlay histograms represent intracellular staining for OVA ( d , top panels) and e ). RFP fluorescence is shown for LA-OVA and mutLA-OVA cells ( d , bottom panels). Numbers in the histogram overlay represent mean fluorescence intensity. Data are representative of 3 independent experiments.
Anti His Tag Cat, supplied by SouthernBiotech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti+his+antibody/Mouse+Anti-His-Tag-BIOT/pm38005242-200-23-26
Average 93 stars, based on 1 article reviews
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93
Cusabio his tag monoclonal antibody
a , Schematic illustration of the two OVA fusion constructs, LA-OVA (top) and the control mutLA-OVA (bottom). b , Western blot analysis of lysates from transfected and untransfected HeLa cells probed with <t>anti-His</t> (top), anti-OVA (middle) and anti-β-actin (bottom) mAbs. c , Confocal analysis of HeLa cells expressing LA-OVA (left figure, top panels) or mutLA-OVA (left figure, bottom panels). Intensity profiles for OVA (AF647) and phalloidin (AF488) channels across 10 μm (white line indicated in the confocal images) are shown on the right. Scale bars shown in confocal images (left) correspond to a size of 5μm. d - e , Flow cytometry analysis of untransfected and transfected HeLa cells before (live) and after UV treatment (UV). Overlay histograms represent intracellular staining for OVA ( d , top panels) and e ). RFP fluorescence is shown for LA-OVA and mutLA-OVA cells ( d , bottom panels). Numbers in the histogram overlay represent mean fluorescence intensity. Data are representative of 3 independent experiments.
His Tag Monoclonal Antibody, supplied by Cusabio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
his tag monoclonal antibody - by Bioz Stars, 2026-10
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Image Search Results


a , Schematic illustration of the two OVA fusion constructs, LA-OVA (top) and the control mutLA-OVA (bottom). b , Western blot analysis of lysates from transfected and untransfected HeLa cells probed with anti-His (top), anti-OVA (middle) and anti-β-actin (bottom) mAbs. c , Confocal analysis of HeLa cells expressing LA-OVA (left figure, top panels) or mutLA-OVA (left figure, bottom panels). Intensity profiles for OVA (AF647) and phalloidin (AF488) channels across 10 μm (white line indicated in the confocal images) are shown on the right. Scale bars shown in confocal images (left) correspond to a size of 5μm. d - e , Flow cytometry analysis of untransfected and transfected HeLa cells before (live) and after UV treatment (UV). Overlay histograms represent intracellular staining for OVA ( d , top panels) and e ). RFP fluorescence is shown for LA-OVA and mutLA-OVA cells ( d , bottom panels). Numbers in the histogram overlay represent mean fluorescence intensity. Data are representative of 3 independent experiments.

Journal: Nature Immunology

Article Title: Cross-presentation of dead cell-associated antigens shapes the neoantigenic landscape of tumor immunity

doi: 10.1038/s41590-025-02354-w

Figure Lengend Snippet: a , Schematic illustration of the two OVA fusion constructs, LA-OVA (top) and the control mutLA-OVA (bottom). b , Western blot analysis of lysates from transfected and untransfected HeLa cells probed with anti-His (top), anti-OVA (middle) and anti-β-actin (bottom) mAbs. c , Confocal analysis of HeLa cells expressing LA-OVA (left figure, top panels) or mutLA-OVA (left figure, bottom panels). Intensity profiles for OVA (AF647) and phalloidin (AF488) channels across 10 μm (white line indicated in the confocal images) are shown on the right. Scale bars shown in confocal images (left) correspond to a size of 5μm. d - e , Flow cytometry analysis of untransfected and transfected HeLa cells before (live) and after UV treatment (UV). Overlay histograms represent intracellular staining for OVA ( d , top panels) and e ). RFP fluorescence is shown for LA-OVA and mutLA-OVA cells ( d , bottom panels). Numbers in the histogram overlay represent mean fluorescence intensity. Data are representative of 3 independent experiments.

Article Snippet: HRP-conjugated goat-anti-rabbit and HRP-conjugated mouse-anti-His-Tag antibodies were from Southern Biotech.

Techniques: Construct, Control, Western Blot, Transfection, Expressing, Flow Cytometry, Staining, Fluorescence