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ng2 apc mouse antihuman  (R&D Systems)


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    R&D Systems ng2 apc mouse antihuman
    FIG. 1. Culture and identification of hOPCs. The transplanted cells were identified based on their morphology and main markers. (A) Identification of the bright field morphology of hOPCs. Scale bar is 200 mm, inset 100 mm. (B) Flow cytometry to detect PDGFR-a, A2B5, <t>NG2,</t> and Ki67 of hOPCs. (C) Tissue immunofluorescence staining to detect PDGFR-a, A2B5, NG2, and Ki67 of transplanted hOPCs. Scale bar is 100 mm. A2B5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1; hOPCs, human–derived oligodendrocyte precursor cells; PDGFR-a, platelet-derived growth factor receptor alpha; NG2, chondroitin sulfate proteoglycan 4.
    Ng2 Apc Mouse Antihuman, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 13 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+antihuman+ng2+antibody+apc+conjugated/Human+NG2%2FMCSP+APC-conjugated+Antibody/pm33823616-49-25-31
    Average 92 stars, based on 13 article reviews
    ng2 apc mouse antihuman - by Bioz Stars, 2026-09
    92/100 stars

    Images

    1) Product Images from "Study on the Safety of Human Oligodendrocyte Precursor Cell Transplantation in Young Animals and Its Efficacy on Myelination."

    Article Title: Study on the Safety of Human Oligodendrocyte Precursor Cell Transplantation in Young Animals and Its Efficacy on Myelination.

    Journal: Stem cells and development

    doi: 10.1089/scd.2021.0012

    FIG. 1. Culture and identification of hOPCs. The transplanted cells were identified based on their morphology and main markers. (A) Identification of the bright field morphology of hOPCs. Scale bar is 200 mm, inset 100 mm. (B) Flow cytometry to detect PDGFR-a, A2B5, NG2, and Ki67 of hOPCs. (C) Tissue immunofluorescence staining to detect PDGFR-a, A2B5, NG2, and Ki67 of transplanted hOPCs. Scale bar is 100 mm. A2B5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1; hOPCs, human–derived oligodendrocyte precursor cells; PDGFR-a, platelet-derived growth factor receptor alpha; NG2, chondroitin sulfate proteoglycan 4.
    Figure Legend Snippet: FIG. 1. Culture and identification of hOPCs. The transplanted cells were identified based on their morphology and main markers. (A) Identification of the bright field morphology of hOPCs. Scale bar is 200 mm, inset 100 mm. (B) Flow cytometry to detect PDGFR-a, A2B5, NG2, and Ki67 of hOPCs. (C) Tissue immunofluorescence staining to detect PDGFR-a, A2B5, NG2, and Ki67 of transplanted hOPCs. Scale bar is 100 mm. A2B5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1; hOPCs, human–derived oligodendrocyte precursor cells; PDGFR-a, platelet-derived growth factor receptor alpha; NG2, chondroitin sulfate proteoglycan 4.

    Techniques Used: Flow Cytometry, Staining, Derivative Assay

    Related Articles

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    Article Title: Spontaneous differentiation of periodontal ligament stem cells into myofibroblast during ex vivo expansion.
    Article Snippet: Institute of Dental Research, Osaka Dental University, Osaka, Japan Department of Nanomedicine (DNP), Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan Department of Periodontology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University (TMDU), Tokyo, Japan Yokohama Clinic, Kanagawa Dental University, Yokohama, Kanagawa, Japan Biomaterial Laboratory, Research and Development Center, Dai Nippon Printing Co., Ltd., Kashiwa, Chiba, Japan Biochemistry, Graduate School of Medical and Dental Science, Tokyo Medical and Dental University (TMDU), Tokyo, Japan Ochanomizu University, Tokyo, Japan



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    ng2 apc mouse antihuman  (R&D Systems)
    92
    R&D Systems ng2 apc mouse antihuman
    FIG. 1. Culture and identification of hOPCs. The transplanted cells were identified based on their morphology and main markers. (A) Identification of the bright field morphology of hOPCs. Scale bar is 200 mm, inset 100 mm. (B) Flow cytometry to detect PDGFR-a, A2B5, <t>NG2,</t> and Ki67 of hOPCs. (C) Tissue immunofluorescence staining to detect PDGFR-a, A2B5, NG2, and Ki67 of transplanted hOPCs. Scale bar is 100 mm. A2B5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1; hOPCs, human–derived oligodendrocyte precursor cells; PDGFR-a, platelet-derived growth factor receptor alpha; NG2, chondroitin sulfate proteoglycan 4.
    Ng2 Apc Mouse Antihuman, supplied by R&D Systems, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+antihuman+ng2+antibody+apc+conjugated/Human+NG2%2FMCSP+APC-conjugated+Antibody/pm33823616-49-25-31
    Average 92 stars, based on 1 article reviews
    ng2 apc mouse antihuman - by Bioz Stars, 2026-09
    92/100 stars
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    mouse antihuman ng2 antibody apc conjugated  (R&D Systems)
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    FIG. 1. Culture and identification of hOPCs. The transplanted cells were identified based on their morphology and main markers. (A) Identification of the bright field morphology of hOPCs. Scale bar is 200 mm, inset 100 mm. (B) Flow cytometry to detect PDGFR-a, A2B5, <t>NG2,</t> and Ki67 of hOPCs. (C) Tissue immunofluorescence staining to detect PDGFR-a, A2B5, NG2, and Ki67 of transplanted hOPCs. Scale bar is 100 mm. A2B5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1; hOPCs, human–derived oligodendrocyte precursor cells; PDGFR-a, platelet-derived growth factor receptor alpha; NG2, chondroitin sulfate proteoglycan 4.
    Mouse Antihuman Ng2 Antibody Apc Conjugated, supplied by R&D Systems, 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+antihuman+ng2+antibody+apc+conjugated/Human+NG2%2FMCSP+APC-conjugated+Antibody/pm30963561-73-0-5
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    mouse antihuman ng2 antibody apc conjugated - by Bioz Stars, 2026-09
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    Image Search Results


    FIG. 1. Culture and identification of hOPCs. The transplanted cells were identified based on their morphology and main markers. (A) Identification of the bright field morphology of hOPCs. Scale bar is 200 mm, inset 100 mm. (B) Flow cytometry to detect PDGFR-a, A2B5, NG2, and Ki67 of hOPCs. (C) Tissue immunofluorescence staining to detect PDGFR-a, A2B5, NG2, and Ki67 of transplanted hOPCs. Scale bar is 100 mm. A2B5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1; hOPCs, human–derived oligodendrocyte precursor cells; PDGFR-a, platelet-derived growth factor receptor alpha; NG2, chondroitin sulfate proteoglycan 4.

    Journal: Stem cells and development

    Article Title: Study on the Safety of Human Oligodendrocyte Precursor Cell Transplantation in Young Animals and Its Efficacy on Myelination.

    doi: 10.1089/scd.2021.0012

    Figure Lengend Snippet: FIG. 1. Culture and identification of hOPCs. The transplanted cells were identified based on their morphology and main markers. (A) Identification of the bright field morphology of hOPCs. Scale bar is 200 mm, inset 100 mm. (B) Flow cytometry to detect PDGFR-a, A2B5, NG2, and Ki67 of hOPCs. (C) Tissue immunofluorescence staining to detect PDGFR-a, A2B5, NG2, and Ki67 of transplanted hOPCs. Scale bar is 100 mm. A2B5, ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1; hOPCs, human–derived oligodendrocyte precursor cells; PDGFR-a, platelet-derived growth factor receptor alpha; NG2, chondroitin sulfate proteoglycan 4.

    Article Snippet: HOPCs were surface stained with PDGFR-aBV421 mouse antihuman (Cat. #562799; BD Biosciences, Franklin Lake, NJ), A2B5 PE mouse anti-human (Cat. #130-093-581; Miltenyi Biotec, Bergisch-Gladbach, Germany), NG2 APC mouse antihuman (Cat. #FAB2585A; R&D Systems, Minnesota), and Ki67 PE mouse anti-human (Cat. # ab270650; Abcam, Cambridge, UK) antibodies for flow cytometry (FACSanto II; BD Biosciences).

    Techniques: Flow Cytometry, Staining, Derivative Assay