mouse anti mhc Search Results


95
Miltenyi Biotec anti mhc ii
Anti Mhc Ii, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems anti mhc class i
Anti Mhc Class I, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Elabscience Biotechnology major histocompatibility complex class ii mchii e ab f0990e
Major Histocompatibility Complex Class Ii Mchii E Ab F0990e, supplied by Elabscience Biotechnology, 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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Miltenyi Biotec rat anti mouse mhc ii microbeads
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Cytek Biosciences apc cyanine7 anti mouse mhc class ii i a i e
Apc Cyanine7 Anti Mouse Mhc Class Ii I A I E, supplied by Cytek Biosciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cytek Biosciences anti mouse mhcii
CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse <t>MHCII</t> and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .
Anti Mouse Mhcii, supplied by Cytek Biosciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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93
Bio-Rad mhc ii
CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse <t>MHCII</t> and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .
Mhc Ii, supplied by Bio-Rad, 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+mhc/Mouse+anti+Rat+MHC+Class+II+RT1B/pm33594532-57-44-49
Average 93 stars, based on 1 article reviews
mhc ii - by Bioz Stars, 2026-09
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93
Bio-Rad anti mhc class ii
CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse <t>MHCII</t> and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .
Anti Mhc Class Ii, supplied by Bio-Rad, 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+mhc/Rat+anti+Mouse+MHC+Class+II+H-2I-Ak%2FD%2FB%2FQ%2FR/pmc12271317-56-6-9
Average 93 stars, based on 1 article reviews
anti mhc class ii - by Bioz Stars, 2026-09
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93
Bio-Rad mouse anti horse major histocompatibility complex mhc class ii
CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse <t>MHCII</t> and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .
Mouse Anti Horse Major Histocompatibility Complex Mhc Class Ii, supplied by Bio-Rad, 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
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94
Bio X Cell mhc i
CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse <t>MHCII</t> and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .
Mhc I, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti+mhc/InVivoMAb+anti-mouse+MHC+Class+I/pmc12715064-49-22-24
Average 94 stars, based on 1 article reviews
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95
Bio X Cell invivomab anti mouse mhc class ii
CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse <t>MHCII</t> and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .
Invivomab Anti Mouse Mhc Class Ii, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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92
Bio X Cell anti h 2k b
CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse <t>MHCII</t> and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .
Anti H 2k B, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse MHCII and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .

Journal: Communications Biology

Article Title: Platelet extracellular vesicles preserve lymphatic endothelial cell integrity and enhance lymphatic vessel function

doi: 10.1038/s42003-024-06675-8

Figure Lengend Snippet: CellVue + human PEVs (1 × 10 7 ) or vehicle control were injected in the dermis of the footpad in wild-type mice. Lymph nodes (LNs) draining the site of injection (green boxes) and LNs located at a distal site (beige boxes) were collected 15 min and 2 h post-injection. Then, they were ( a ) visualized with a fluorescence imaging scanner (IVIS Lumina II) or ( b ) digested with collagenase D to determine the percentage of cells containing EVs. c The concentration of free EVs within the LNs were assessed by flow cytometry using anti-mouse MHCII and anti-human CD62P antibodies. d Two hours post-PEV injection, popliteal lymphatic vessels draining the injection site were also collected, harvested and stained with anti-human CD41a antibody (red) and DAPI (blue) to be imaged with a confocal microscope (white scale bar, 20 µm). The lymphatic contraction capacity was measured in vivo 48 h after the injection of ( e ) PEVs or ( f ) rbEVs in Ldlr -/- , and ( g ) after injection of PEVs in wild-type mice. h The lymph nodes (N-D, beige; D, green) and ( i ) the aorta were also collected at 48 h and visualized with fluorescent imaging. Each point represents a mouse ± SEM. N-D: non-draining; D: draining; LN: lymph nodes; EVs: extracellular vesicles. PEVs: platelet extracellular vesicles. rbEVs: red blood cell extracellular vesicles. Created with Biorender.com .

Article Snippet: To identify the proportion of LN cells positive in PEVs, cells were resuspended in HBSS buffer supplemented with 0.5 M EDTA and 30% bovine serum albumin (BSA) and stained for 30 min at 4 °C with anti-mouse CD45 (FITC, Tonbo Biosciences cat. #350451), anti-mouse MHCII (V450, Tonbo Biosciences cat. #755321) and anti-human CD62P (PE, BioLegends cat. #304905) antibodies (Supplementary Fig. ).

Techniques: Control, Injection, Fluorescence, Imaging, Concentration Assay, Flow Cytometry, Staining, Microscopy, In Vivo