smooth muscle alpha actin ap vector blue vimentin Search Results


horseradish peroxidase streptavidin  (Vector Laboratories)
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Vector Laboratories horseradish peroxidase streptavidin
Horseradish Peroxidase Streptavidin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rabbit antigoat igg biotin  (Vector Laboratories)
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polyclonal antibody  (Cell Signaling Technology Inc)
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Cell Signaling Technology Inc polyclonal antibody
Polyclonal Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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alpha smooth muscle actin  (Danaher Inc)
99
Danaher Inc alpha smooth muscle actin
Alpha Smooth Muscle Actin, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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horseradish peroxidase hrp conjugated abc  (Vector Laboratories)
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Vector Laboratories horseradish peroxidase hrp conjugated abc
Horseradish Peroxidase Hrp Conjugated Abc, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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antibodies against human spectrin  (Vector Laboratories)
96
Vector Laboratories antibodies against human spectrin
Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), <t>human</t> <t>spectrin</t> (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.
Antibodies Against Human Spectrin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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antibodies against human spectrin - by Bioz Stars, 2026-11
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eda fibronectin  (Vector Laboratories)
96
Vector Laboratories eda fibronectin
Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), <t>human</t> <t>spectrin</t> (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.
Eda Fibronectin, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse monoclonal anti α muscle actin α sma  (Vector Laboratories)
95
Vector Laboratories mouse monoclonal anti α muscle actin α sma
Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), <t>human</t> <t>spectrin</t> (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.
Mouse Monoclonal Anti α Muscle Actin α Sma, supplied by Vector Laboratories, 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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mouse monoclonal anti α muscle actin α sma - by Bioz Stars, 2026-11
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avidinbiotin horseradish peroxidase complex  (Vector Laboratories)
96
Vector Laboratories avidinbiotin horseradish peroxidase complex
Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), <t>human</t> <t>spectrin</t> (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.
Avidinbiotin Horseradish Peroxidase Complex, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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avidinbiotin horseradish peroxidase complex - by Bioz Stars, 2026-11
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horseradish peroxidase hrp  (Vector Laboratories)
96
Vector Laboratories horseradish peroxidase hrp
Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), <t>human</t> <t>spectrin</t> (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.
Horseradish Peroxidase Hrp, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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vectastain abc kit  (Vector Laboratories)
96
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Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), <t>human</t> <t>spectrin</t> (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.
Vectastain Abc Kit, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti alpha smooth muscle actin antibody 1 50  (Vector Laboratories)
96
Vector Laboratories anti alpha smooth muscle actin antibody 1 50
Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), <t>human</t> <t>spectrin</t> (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.
Anti Alpha Smooth Muscle Actin Antibody 1 50, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), human spectrin (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.

Journal: Molecular therapy. Methods & clinical development

Article Title: Optimized lentiviral vector to restore full-length dystrophin via a cell-mediated approach in a mouse model of Duchenne muscular dystrophy.

doi: 10.1016/j.omtm.2022.04.015

Figure Lengend Snippet: Figure 4. Restoration of dystrophin by lentivirally transduced cells in vivo. DMD-NT, DMD-nFLDys and DMD-soFLDys myoblasts were transplanted into cryoinjured muscles of mdx nude mice Muscle sections were stained for human laminAC (red), human spectrin (red) and human dystrophin (green) to determine the transplantation efficiency and the extent of dystrophin restoration in vivo. Muscles transplanted with normal myoblasts were used as control. (A) Transplantation efficiency of the DMD-NT, DMD-nFLDys and DMD- soFLDys were comparable, as determined by the number of human lamin AC+ nuclei (a), human spectrin+ fibres (b) and human spectrin+ fibres containing at least one human laminAC+ nucleus (S+L) (c). (B) Representative images of the donor fibres (human spectrin+, red) expressing dystrophin (Mandys106, green) in each transplantation group. Nuclei were stained with DAPI (blue). Scale bar=50mm. There were significantly more human dystrophin+ fibres (C) and a higher percentage of human dystrophin+/ hSpectrin+ fibres (D) in DMD-soFLDys group than in DMD-nFLDys group. The relative intensity (E) of the human dystrophin was also significantly higher in DMD-soFLDys group than in DMD-nFLDys group, and the intensity of the human dystrophin was comparable to that of normal myoblast transplanted group. *p<0.05, **p<0.01.

Article Snippet: Transverse cryosections (10 mm) were air dried and blocked with AffiniPure F(ab0)2 fragment donkey anti-mouse IgG (H + L) (1:50; Jackson Immuno Research, Cambridge, UK) for 1 h at room temperature and stained with the following combinations of antibodies: (1) antibodies against human spectrin (mouse IgG 2b; Vector Labs, VP-S283, 1:100, Peterborough, UK), human lamin A/C (mouse IgG2b; Vector Labs, VP-L550, 1:500, Peterborough, UK), and human dystrophin (Mandys 106, mouse IgG2a, 1:200; Millipore).

Techniques: In Vivo, Muscles, Staining, Transplantation Assay, Control, Expressing