lectin 594 conjugate Search Results


rhodamine labeled peanut agglutinin (pna)  (Vector Laboratories)
94
Vector Laboratories rhodamine labeled peanut agglutinin (pna)
Rhodamine Labeled Peanut Agglutinin (Pna), supplied by Vector Laboratories, 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/result/rhodamine labeled peanut agglutinin (pna)/product/Vector Laboratories
Average 94 stars, based on 1 article reviews
rhodamine labeled peanut agglutinin (pna) - by Bioz Stars, 2026-03
94/100 stars
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tomato lectin dylight 594-conjugated lycopersion esculentum lectin  (Funakoshi ltd)
90
Funakoshi ltd tomato lectin dylight 594-conjugated lycopersion esculentum lectin
a Schematic overview of the protocol used to construct the vascular bed. GFs, growth factors. b A gelatin sheet before incubation with growth factors. c The gelatin sheet after incubation with growth factors at 4 °C for 24 h. d Azan staining of the gelatin sheet before incubation. e The vascular bed (VB) in the GF(−) group (gelatin sheet not pre-loaded with growth factors) 21 days after incubation in vivo. f The vascular bed (VB) in the GF(+) group (gelatin sheet pre-loaded with growth factors) 21 days after incubation in vivo. g Section of the vascular bed (VB) in the GF(−) group stained with hematoxylin and eosin (HE) on day 21. h Section of the vascular bed (VB) in the GF(+) group stained with HE on day 21. The region around the SFA and SFV contained new blood vessels rich in smooth muscle. i, <t>k</t> <t>Fluorescent</t> beads (4 μm diameter) were administered into the SFA and vascular bed via a catheter inserted through the abdominal aorta and advanced into the femoral artery (day 21). New blood vessels in the gelatin gel were more extensive in the FA(+) GF(+) group (gelatin sheet pre-loaded with growth factors, SFA occluded after 14 days of incubation in vivo) than in the FA(−) GF(+) group or FA(+) GF(−) group. l , m Tomato <t>lectin</t> (to label vascular endothelial cells) and fluorescent beads (to reveal blood flow) were administered to a vascular bed from the FA(+) GF(+) group and observed using two-photon microscopy. Endothelial cells in the gelatin sheet formed a network of vascular structures through which fluorescent beads passed. n , o Tomato lectin (to label vascular endothelial cells) and Hoechst solution (to label nuclei) were administered to a vascular bed from the FA(+) GF(+) group and observed using two-photon microscopy. The new blood vessels contained structures resembling tip cells and stalk cells. Stained nuclei were observed at the tips of the extending blood vessels. p Capillary density in the vascular bed (mean ± SEM). q Smooth muscle cell area in the vascular bed (mean ± SEM).
Tomato Lectin Dylight 594 Conjugated Lycopersion Esculentum Lectin, supplied by Funakoshi ltd, 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/tomato lectin dylight 594-conjugated lycopersion esculentum lectin/product/Funakoshi ltd
Average 90 stars, based on 1 article reviews
tomato lectin dylight 594-conjugated lycopersion esculentum lectin - by Bioz Stars, 2026-03
90/100 stars
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a Schematic overview of the protocol used to construct the vascular bed. GFs, growth factors. b A gelatin sheet before incubation with growth factors. c The gelatin sheet after incubation with growth factors at 4 °C for 24 h. d Azan staining of the gelatin sheet before incubation. e The vascular bed (VB) in the GF(−) group (gelatin sheet not pre-loaded with growth factors) 21 days after incubation in vivo. f The vascular bed (VB) in the GF(+) group (gelatin sheet pre-loaded with growth factors) 21 days after incubation in vivo. g Section of the vascular bed (VB) in the GF(−) group stained with hematoxylin and eosin (HE) on day 21. h Section of the vascular bed (VB) in the GF(+) group stained with HE on day 21. The region around the SFA and SFV contained new blood vessels rich in smooth muscle. i, k Fluorescent beads (4 μm diameter) were administered into the SFA and vascular bed via a catheter inserted through the abdominal aorta and advanced into the femoral artery (day 21). New blood vessels in the gelatin gel were more extensive in the FA(+) GF(+) group (gelatin sheet pre-loaded with growth factors, SFA occluded after 14 days of incubation in vivo) than in the FA(−) GF(+) group or FA(+) GF(−) group. l , m Tomato lectin (to label vascular endothelial cells) and fluorescent beads (to reveal blood flow) were administered to a vascular bed from the FA(+) GF(+) group and observed using two-photon microscopy. Endothelial cells in the gelatin sheet formed a network of vascular structures through which fluorescent beads passed. n , o Tomato lectin (to label vascular endothelial cells) and Hoechst solution (to label nuclei) were administered to a vascular bed from the FA(+) GF(+) group and observed using two-photon microscopy. The new blood vessels contained structures resembling tip cells and stalk cells. Stained nuclei were observed at the tips of the extending blood vessels. p Capillary density in the vascular bed (mean ± SEM). q Smooth muscle cell area in the vascular bed (mean ± SEM).

Journal: NPJ Regenerative Medicine

Article Title: Bioartificial pulsatile cuffs fabricated from human induced pluripotent stem cell-derived cardiomyocytes using a pre-vascularization technique

doi: 10.1038/s41536-022-00218-7

Figure Lengend Snippet: a Schematic overview of the protocol used to construct the vascular bed. GFs, growth factors. b A gelatin sheet before incubation with growth factors. c The gelatin sheet after incubation with growth factors at 4 °C for 24 h. d Azan staining of the gelatin sheet before incubation. e The vascular bed (VB) in the GF(−) group (gelatin sheet not pre-loaded with growth factors) 21 days after incubation in vivo. f The vascular bed (VB) in the GF(+) group (gelatin sheet pre-loaded with growth factors) 21 days after incubation in vivo. g Section of the vascular bed (VB) in the GF(−) group stained with hematoxylin and eosin (HE) on day 21. h Section of the vascular bed (VB) in the GF(+) group stained with HE on day 21. The region around the SFA and SFV contained new blood vessels rich in smooth muscle. i, k Fluorescent beads (4 μm diameter) were administered into the SFA and vascular bed via a catheter inserted through the abdominal aorta and advanced into the femoral artery (day 21). New blood vessels in the gelatin gel were more extensive in the FA(+) GF(+) group (gelatin sheet pre-loaded with growth factors, SFA occluded after 14 days of incubation in vivo) than in the FA(−) GF(+) group or FA(+) GF(−) group. l , m Tomato lectin (to label vascular endothelial cells) and fluorescent beads (to reveal blood flow) were administered to a vascular bed from the FA(+) GF(+) group and observed using two-photon microscopy. Endothelial cells in the gelatin sheet formed a network of vascular structures through which fluorescent beads passed. n , o Tomato lectin (to label vascular endothelial cells) and Hoechst solution (to label nuclei) were administered to a vascular bed from the FA(+) GF(+) group and observed using two-photon microscopy. The new blood vessels contained structures resembling tip cells and stalk cells. Stained nuclei were observed at the tips of the extending blood vessels. p Capillary density in the vascular bed (mean ± SEM). q Smooth muscle cell area in the vascular bed (mean ± SEM).

Article Snippet: Tomato lectin (DyLight 594-conjugated Lycopersion esculentum Lectin; Funakoshi) and fluorescent beads (FluoSpheres TM sulfate, 4.0 μm, yellow-green; Life Technologies) were administered via the catheter (1 mL of each, diluted tenfold), and the proximal SFA and SFV were ligated with 6-0 silk to prevent the loss of the injected markers from the vascular bed.

Techniques: Construct, Incubation, Staining, In Vivo, Microscopy