subdermal 29 g needle electrodes Search Results


recording electrodes  (ADInstruments)
96
ADInstruments recording electrodes
Recording Electrodes, supplied by ADInstruments, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/recording electrodes/product/ADInstruments
Average 96 stars, based on 1 article reviews
recording electrodes - by Bioz Stars, 2026-04
96/100 stars
  Buy from Supplier
needle electrodes mla1204  (ADInstruments)
90
ADInstruments needle electrodes mla1204
Needle Electrodes Mla1204, supplied by ADInstruments, 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/needle electrodes mla1204/product/ADInstruments
Average 90 stars, based on 1 article reviews
needle electrodes mla1204 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
needle electrodes 29g  (ADInstruments)
90
ADInstruments needle electrodes 29g
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
Needle Electrodes 29g, supplied by ADInstruments, 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/needle electrodes 29g/product/ADInstruments
Average 90 stars, based on 1 article reviews
needle electrodes 29g - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
recording electrodes 29 g needle mla1213  (ADInstruments)
90
ADInstruments recording electrodes 29 g needle mla1213
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
Recording Electrodes 29 G Needle Mla1213, supplied by ADInstruments, 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/recording electrodes 29 g needle mla1213/product/ADInstruments
Average 90 stars, based on 1 article reviews
recording electrodes 29 g needle mla1213 - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
ra-ni (h2o)  (Fluka Chemical)
90
Fluka Chemical ra-ni (h2o)
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
Ra Ni (H2o), supplied by Fluka Chemical, 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/ra-ni (h2o)/product/Fluka Chemical
Average 90 stars, based on 1 article reviews
ra-ni (h2o) - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
29-g catheter  (ReCathCo Inc)
90
ReCathCo Inc 29-g catheter
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
29 G Catheter, supplied by ReCathCo Inc, 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/29-g catheter/product/ReCathCo Inc
Average 90 stars, based on 1 article reviews
29-g catheter - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
29-g navitip needles  (Ultradent Products Inc)
90
Ultradent Products Inc 29-g navitip needles
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
29 G Navitip Needles, supplied by Ultradent Products Inc, 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/29-g navitip needles/product/Ultradent Products Inc
Average 90 stars, based on 1 article reviews
29-g navitip needles - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
syringe 29-g needle  (Hamilton Bonaduz)
90
Hamilton Bonaduz syringe 29-g needle
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
Syringe 29 G Needle, supplied by Hamilton Bonaduz, 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/syringe 29-g needle/product/Hamilton Bonaduz
Average 90 stars, based on 1 article reviews
syringe 29-g needle - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
insulin syringe 29-g needle  (Becton Dickinson)
90
Becton Dickinson insulin syringe 29-g needle
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
Insulin Syringe 29 G Needle, supplied by Becton Dickinson, 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/insulin syringe 29-g needle/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
insulin syringe 29-g needle - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
29-g syringe needle  (Terumo Corp)
90
Terumo Corp 29-g syringe needle
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
29 G Syringe Needle, supplied by Terumo Corp, 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/29-g syringe needle/product/Terumo Corp
Average 90 stars, based on 1 article reviews
29-g syringe needle - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
insulin 29-g u-100 needle  (BD Diagnostics)
90
BD Diagnostics insulin 29-g u-100 needle
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
Insulin 29 G U 100 Needle, supplied by BD Diagnostics, 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/insulin 29-g u-100 needle/product/BD Diagnostics
Average 90 stars, based on 1 article reviews
insulin 29-g u-100 needle - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
29½g insulin syringe  (Becton Dickinson)
90
Becton Dickinson 29½g insulin syringe
Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle <t>electrodes</t> were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.
29½g Insulin Syringe, supplied by Becton Dickinson, 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/29½g insulin syringe/product/Becton Dickinson
Average 90 stars, based on 1 article reviews
29½g insulin syringe - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

Image Search Results


Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle electrodes were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.

Journal: Regenerative Therapy

Article Title: Generation of a large-scale vascular bed for the in vitro creation of three-dimensional cardiac tissue

doi: 10.1016/j.reth.2019.10.001

Figure Lengend Snippet: Cardiac cell sheet implantation . (a) An endothelial cell network (evaluated from the expression of CD31, an endothelial cell marker) was clearly detected following the co-culture of green fluorescent protein (GFP)-expressing human umbilical vein endothelial cells (HUVECs) with adult normal human dermal fibroblasts (NHDFs) at a ratio of 10:1. cTnT: cardiac troponin T. (b) An endothelial cell network was not detected after the co-culture of cardiomyocytes derived from human induced pluripotent stem cells (hiPSCs) and GFP-positive HUVECs. CM: cardiomyocytes. (c) An endothelial cell network was created when cardiomyocytes were co-cultured with GFP-positive HUVECs and NHDFs at a ratio of 5:1:5. (d) Cardiomyocytes derived from hiPSCs were co-cultured with GFP-positive HUVECs in a temperature-responsive dish and harvested as a monolayer sheet. The harvested sheet shrank to approximately one-third of the dish diameter. (e) Three harvested cardiac cell sheets were layered, and this triple-layered cell sheet (broken circle) was placed onto a vascular bed created from porcine small intestine (day 0). The fabricated tissue construct was then subjected to perfusion culture for 6 days. (f) Needle electrodes were used to record surface action potentials from the implanted cardiac cell sheet (broken circle) after 6 days of perfusion culture. (g) Representative trace showing surface action potentials recorded from the implanted cardiac cell sheet after 6 days of perfusion culture. The implanted cardiac cell sheet was observed to beat spontaneously with a regular rhythm.

Article Snippet: The bioreactor was opened, and two needle electrodes (29G in diameter; ADInstruments, New South Wales, Australia) were placed over the cardiac tissue.

Techniques: Expressing, Marker, Co-Culture Assay, Derivative Assay, Cell Culture, Construct