bs-13135R-BF647 Search Results


lyve 1  (Bioss)
90
Bioss lyve 1
Cells for in vitro culture were positively selected with Lycopersicon esculentum agglutinin (endothelial cells), and <t>LYVE-1</t> (lymphatic endothelial cells) during the proliferation phase. Cells were characterized by flow cytometry after digestion and staining. In this representative example, 94.2% of cells were LIVE cells. Of that population, 97% were endothelial cells (CD141+) and not leukocytes (CD45−). Of this population 94.2% were Prox-1+, a unique intracellular lymphatic endothelial cell marker. This example was from 8th passage lymphatic endothelial cells.
Lyve 1, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
lyve 1 - by Bioz Stars, 2026-02
90/100 stars
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fakd3 polyclonal antibody, abby fluor 647 conjugated  (Bioss)
N/A
FAKD3 is a member of a small family of Fas-activated serine/threonine kinase domain (FASTKD) containing proteins that share an amino terminal mitochondrial targeting domain and multiple carboxy terminal FAST domains as well as a putative
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Cells for in vitro culture were positively selected with Lycopersicon esculentum agglutinin (endothelial cells), and LYVE-1 (lymphatic endothelial cells) during the proliferation phase. Cells were characterized by flow cytometry after digestion and staining. In this representative example, 94.2% of cells were LIVE cells. Of that population, 97% were endothelial cells (CD141+) and not leukocytes (CD45−). Of this population 94.2% were Prox-1+, a unique intracellular lymphatic endothelial cell marker. This example was from 8th passage lymphatic endothelial cells.

Journal: Angiogenesis

Article Title: Lymphangiogenesis in rat asthma model

doi: 10.1007/s10456-016-9529-2

Figure Lengend Snippet: Cells for in vitro culture were positively selected with Lycopersicon esculentum agglutinin (endothelial cells), and LYVE-1 (lymphatic endothelial cells) during the proliferation phase. Cells were characterized by flow cytometry after digestion and staining. In this representative example, 94.2% of cells were LIVE cells. Of that population, 97% were endothelial cells (CD141+) and not leukocytes (CD45−). Of this population 94.2% were Prox-1+, a unique intracellular lymphatic endothelial cell marker. This example was from 8th passage lymphatic endothelial cells.

Article Snippet: LYVE-1 , Alexa Fluor 647, rabbit polyclonal, bs-1311R0A647 , Bioss.

Techniques: In Vitro, Flow Cytometry, Staining, Marker

Green staining is anti-LYVE-1 (lymphatics), red is Griffonia simplicifolia lectin (pulmonary artery; PA), and blue is DAPI (all cell nuclei). White arrows indicate lymphatic vessels. In the control rats, lymphatics are seen in the interstitial space between airways and pulmonary arteries, whereas in lungs from HDM sensitized rats, additional lymphatics appear all around the airway wall. Bar = 50 μm

Journal: Angiogenesis

Article Title: Lymphangiogenesis in rat asthma model

doi: 10.1007/s10456-016-9529-2

Figure Lengend Snippet: Green staining is anti-LYVE-1 (lymphatics), red is Griffonia simplicifolia lectin (pulmonary artery; PA), and blue is DAPI (all cell nuclei). White arrows indicate lymphatic vessels. In the control rats, lymphatics are seen in the interstitial space between airways and pulmonary arteries, whereas in lungs from HDM sensitized rats, additional lymphatics appear all around the airway wall. Bar = 50 μm

Article Snippet: LYVE-1 , Alexa Fluor 647, rabbit polyclonal, bs-1311R0A647 , Bioss.

Techniques: Staining

White arrows in left panels indicate region of enhanced magnification in right panels. Arrows in high magnification panels on right indicate sparse anti-LYVE-1 lymphatic endothelial staining (green) in the interstitial area between a pulmonary artery (PA; red: Griffonia simplicifolia lectin) and an airway outlined by DAPI (blue). The HDM section shows more abundant anti-LYVE-1 lymphatic endothelial staining. Left panel bars = 100 μm; Right panel bars= 50 μm

Journal: Angiogenesis

Article Title: Lymphangiogenesis in rat asthma model

doi: 10.1007/s10456-016-9529-2

Figure Lengend Snippet: White arrows in left panels indicate region of enhanced magnification in right panels. Arrows in high magnification panels on right indicate sparse anti-LYVE-1 lymphatic endothelial staining (green) in the interstitial area between a pulmonary artery (PA; red: Griffonia simplicifolia lectin) and an airway outlined by DAPI (blue). The HDM section shows more abundant anti-LYVE-1 lymphatic endothelial staining. Left panel bars = 100 μm; Right panel bars= 50 μm

Article Snippet: LYVE-1 , Alexa Fluor 647, rabbit polyclonal, bs-1311R0A647 , Bioss.

Techniques: Staining

Red, chromagen stained LYVE-1+ vessels (arrows) are sparse in naïve airways (upper images) compared to HDM lung (lower panels). Right panels are increased magnification of left panel regions indicated by arrows. Bar = 100 μm

Journal: Angiogenesis

Article Title: Lymphangiogenesis in rat asthma model

doi: 10.1007/s10456-016-9529-2

Figure Lengend Snippet: Red, chromagen stained LYVE-1+ vessels (arrows) are sparse in naïve airways (upper images) compared to HDM lung (lower panels). Right panels are increased magnification of left panel regions indicated by arrows. Bar = 100 μm

Article Snippet: LYVE-1 , Alexa Fluor 647, rabbit polyclonal, bs-1311R0A647 , Bioss.

Techniques: Staining

A significant increase in the number of LYVE-1+ lymphatic vessels was observed in HDM treated rats compared to naïve rats. Each point represents the number (#) of lymphatic vessels from one rat (n=3 rats/group). * indicates p=0.036

Journal: Angiogenesis

Article Title: Lymphangiogenesis in rat asthma model

doi: 10.1007/s10456-016-9529-2

Figure Lengend Snippet: A significant increase in the number of LYVE-1+ lymphatic vessels was observed in HDM treated rats compared to naïve rats. Each point represents the number (#) of lymphatic vessels from one rat (n=3 rats/group). * indicates p=0.036

Article Snippet: LYVE-1 , Alexa Fluor 647, rabbit polyclonal, bs-1311R0A647 , Bioss.

Techniques: