primary human msc Search Results


94
PromoCell human mesenchymal stem cells
Human Mesenchymal Stem Cells, supplied by PromoCell, 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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Average 94 stars, based on 1 article reviews
human mesenchymal stem cells - by Bioz Stars, 2026-02
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90
Becton Dickinson primary antibodies human msc analysis kit
Characterization of hiPS-MSCs derived extracellular vesicles (hiPS-MSCs-EV) ( A ). Flowchart of <t>hiPS-MSC-EVs</t> isolation from the culture medium. ( B ). Morphology of hiPS-MSC-EVs under transmission electron microscopy. ( C ). Representative bioanalyzer profile of the RNA contained in hiPS-MSC-EVs. ( D ). Western blotting analysis of exosomal positive markers CD63, CD9, and CD81 and negative marker Calnexin in MSC lysate and hiPS-MSC-EVs. Tubulin was used as the loading control. ( E ). Flow cytometry analysis of positive marker CD63 expression after binding to CD9 and CD81 antibody-coated beads. The solid gray line represents cells that were unstained. while solid pink line represents the experimental samples. ( F ). Particle size distribution of iPSC-MSC-EVs measured using a flow nanoanalyzer.
Primary Antibodies Human Msc Analysis Kit, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibodies human msc analysis kit/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
primary antibodies human msc analysis kit - by Bioz Stars, 2026-02
90/100 stars
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90
Jackson Laboratory primary human bone marrow msc
Characterization of hiPS-MSCs derived extracellular vesicles (hiPS-MSCs-EV) ( A ). Flowchart of <t>hiPS-MSC-EVs</t> isolation from the culture medium. ( B ). Morphology of hiPS-MSC-EVs under transmission electron microscopy. ( C ). Representative bioanalyzer profile of the RNA contained in hiPS-MSC-EVs. ( D ). Western blotting analysis of exosomal positive markers CD63, CD9, and CD81 and negative marker Calnexin in MSC lysate and hiPS-MSC-EVs. Tubulin was used as the loading control. ( E ). Flow cytometry analysis of positive marker CD63 expression after binding to CD9 and CD81 antibody-coated beads. The solid gray line represents cells that were unstained. while solid pink line represents the experimental samples. ( F ). Particle size distribution of iPSC-MSC-EVs measured using a flow nanoanalyzer.
Primary Human Bone Marrow Msc, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary human bone marrow msc/product/Jackson Laboratory
Average 90 stars, based on 1 article reviews
primary human bone marrow msc - by Bioz Stars, 2026-02
90/100 stars
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90
Lonza msc culture: passage 2 primary human bone marrow derived mscs
Characterization of hiPS-MSCs derived extracellular vesicles (hiPS-MSCs-EV) ( A ). Flowchart of <t>hiPS-MSC-EVs</t> isolation from the culture medium. ( B ). Morphology of hiPS-MSC-EVs under transmission electron microscopy. ( C ). Representative bioanalyzer profile of the RNA contained in hiPS-MSC-EVs. ( D ). Western blotting analysis of exosomal positive markers CD63, CD9, and CD81 and negative marker Calnexin in MSC lysate and hiPS-MSC-EVs. Tubulin was used as the loading control. ( E ). Flow cytometry analysis of positive marker CD63 expression after binding to CD9 and CD81 antibody-coated beads. The solid gray line represents cells that were unstained. while solid pink line represents the experimental samples. ( F ). Particle size distribution of iPSC-MSC-EVs measured using a flow nanoanalyzer.
Msc Culture: Passage 2 Primary Human Bone Marrow Derived Mscs, supplied by Lonza, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/msc culture: passage 2 primary human bone marrow derived mscs/product/Lonza
Average 90 stars, based on 1 article reviews
msc culture: passage 2 primary human bone marrow derived mscs - by Bioz Stars, 2026-02
90/100 stars
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90
Genetec Inc primary human mesenchymal stem cells (msc) isolated from dental pulp
Characterization of hiPS-MSCs derived extracellular vesicles (hiPS-MSCs-EV) ( A ). Flowchart of <t>hiPS-MSC-EVs</t> isolation from the culture medium. ( B ). Morphology of hiPS-MSC-EVs under transmission electron microscopy. ( C ). Representative bioanalyzer profile of the RNA contained in hiPS-MSC-EVs. ( D ). Western blotting analysis of exosomal positive markers CD63, CD9, and CD81 and negative marker Calnexin in MSC lysate and hiPS-MSC-EVs. Tubulin was used as the loading control. ( E ). Flow cytometry analysis of positive marker CD63 expression after binding to CD9 and CD81 antibody-coated beads. The solid gray line represents cells that were unstained. while solid pink line represents the experimental samples. ( F ). Particle size distribution of iPSC-MSC-EVs measured using a flow nanoanalyzer.
Primary Human Mesenchymal Stem Cells (Msc) Isolated From Dental Pulp, supplied by Genetec Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary human mesenchymal stem cells (msc) isolated from dental pulp/product/Genetec Inc
Average 90 stars, based on 1 article reviews
primary human mesenchymal stem cells (msc) isolated from dental pulp - by Bioz Stars, 2026-02
90/100 stars
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Image Search Results


Characterization of hiPS-MSCs derived extracellular vesicles (hiPS-MSCs-EV) ( A ). Flowchart of hiPS-MSC-EVs isolation from the culture medium. ( B ). Morphology of hiPS-MSC-EVs under transmission electron microscopy. ( C ). Representative bioanalyzer profile of the RNA contained in hiPS-MSC-EVs. ( D ). Western blotting analysis of exosomal positive markers CD63, CD9, and CD81 and negative marker Calnexin in MSC lysate and hiPS-MSC-EVs. Tubulin was used as the loading control. ( E ). Flow cytometry analysis of positive marker CD63 expression after binding to CD9 and CD81 antibody-coated beads. The solid gray line represents cells that were unstained. while solid pink line represents the experimental samples. ( F ). Particle size distribution of iPSC-MSC-EVs measured using a flow nanoanalyzer.

Journal: Biomedicines

Article Title: Neuroprotective Effects of Human-Induced Pluripotent Stem Cell-Derived Mesenchymal Stem Cell Extracellular Vesicles in Ischemic Stroke Models

doi: 10.3390/biomedicines11092550

Figure Lengend Snippet: Characterization of hiPS-MSCs derived extracellular vesicles (hiPS-MSCs-EV) ( A ). Flowchart of hiPS-MSC-EVs isolation from the culture medium. ( B ). Morphology of hiPS-MSC-EVs under transmission electron microscopy. ( C ). Representative bioanalyzer profile of the RNA contained in hiPS-MSC-EVs. ( D ). Western blotting analysis of exosomal positive markers CD63, CD9, and CD81 and negative marker Calnexin in MSC lysate and hiPS-MSC-EVs. Tubulin was used as the loading control. ( E ). Flow cytometry analysis of positive marker CD63 expression after binding to CD9 and CD81 antibody-coated beads. The solid gray line represents cells that were unstained. while solid pink line represents the experimental samples. ( F ). Particle size distribution of iPSC-MSC-EVs measured using a flow nanoanalyzer.

Article Snippet: The cells were incubated with primary antibodies from the human MSC analysis kit (Cat#562245, BD Biosciences, San Jose, CA, USA) to identify the characteristic human MSC surface markers.

Techniques: Derivative Assay, Isolation, Transmission Assay, Electron Microscopy, Western Blot, Marker, Flow Cytometry, Expressing, Binding Assay