lectin 594 conjugate Search Results


mannan binding lectin monoclonal antibody, alexa fluor 594 conjugated  (Bioss)
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phaseolus vulgaris leucoagglutinin (pha-l) lectin, cf 594 conjugate  (Antibodies Inc)
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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/product/lectin+594+conjugate/tomato+lectin+dylight+594+conjugated+lycopersion+esculentum+lectin/pmc08971499-203-0-7
Average 90 stars, based on 1 article reviews
tomato lectin dylight 594-conjugated lycopersion esculentum lectin - by Bioz Stars, 2026-10
90/100 stars
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rhodamine labeled peanut agglutinin (pna)  (Vector Laboratories)
94
Vector Laboratories rhodamine labeled peanut agglutinin (pna)
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).
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/product/lectin+594+conjugate/Rhodamine+labeled+Peanut+Agglutinin+(PNA)/custom%40rl-1072%4029848071
Average 94 stars, based on 1 article reviews
rhodamine labeled peanut agglutinin (pna) - by Bioz Stars, 2026-10
94/100 stars
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plant lectin b4 polyclonal antibody, abby fluor 594 conjugated  (Bioss)
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plant lectin B4
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lectin lca polyclonal antibody, abby fluor 594 conjugated  (Bioss)
N/A
Lens culinaris agglutinin is composed of four subunits - two of about 17 kDa and two of 8 kDa. LCA recognizes sequences containing _-linked mannose residues but recognizes additional sugars as part of the receptor
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lectin from ulex europaeus-atto 594 conjugate  (BOC Sciences)
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Lectins are ubiquitous proteins or glycoproteins with a high and specific affinity to sugar residues. They allow a sensitive detection of cellular carbohydrates, revealing subtle alteration in glycosylation between otherwise indistinguishable cells. ATTO-dyes have very
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mannan binding lectin monoclonal antibody, abby fluor 594 conjugated  (Bioss)
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plant lectin b4 polyclonal antibody, alexa fluor 594 conjugated  (Bioss)
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plant lectin B4
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ulex europaeus lectin 1 antibody, alexa fluor 594 conjugated  (Bioss)
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Ulex Europaeus is a European gorse shrub with fragrant golden-yellow flowers. Ulex Europaeus-I Lectin is a 46 kDa glycoprotein known to interact with -L fucosyl residues in oligosaccharides present on the membranes of human blood
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lycopersicon esculentum (tomato) lectin (lel, tl), cf 594 conjugate  (Antibodies Inc)
N/A
The anti-H (O) hemagglutinating activity of Ulex europaeus has been used widely to confirm blood group O activity. UEA I binds to many glycoproteins and glycolipids containing α –linked fucose residue. The purified lectin appears
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lectin lca polyclonal antibody, alexa fluor 594 conjugated  (Bioss)
N/A
Lens culinaris agglutinin is composed of four subunits - two of about 17 kDa and two of 8 kDa. LCA recognizes sequences containing _-linked mannose residues but recognizes additional sugars as part of the receptor
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Image Search Results


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