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ReproCELL primate es ips cells
Primate Es Ips Cells, supplied by ReproCELL, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/detachment/Primate+ES+cell+medium/us09574165-211-33-42
Average 95 stars, based on 1 article reviews
primate es ips cells - by Bioz Stars, 2026-10
95/100 stars

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Cell Culture:

Article Title: Method of producing pancreatic hormone-producing cells
Article Snippet: .. First, human iPS cells (iPS cells obtained by introducing Oct3/4gene, Klf4 gene and Sox2 gene: see Nat Biotechnol 2008; 26: 101-106) cultured and maintained in the state of a cell mass together with feeder cells were detached in the state of a cell mass by using a cell dissociation solution for primate ES cell (ReproCELL Inc.), these cells were transferred into a 15 ml centrifuge tube and stood for 5 min. ..

Article Title: Human pluripotent stem cells induced from undifferentiated stem cells derived from a human postnatal tissue
Article Snippet: .. One hundred μl of the Detachment Medium For Primate ES Cells (manufactured by ReproCELL) was added in the ring and cultured at 37° C. for 20 minutes. ..

Article Title: Human pluripotent stem cells induced from undifferentiated stem cells derived from a human postnatal tissue
Article Snippet: .. The medium was removed, washed with the Hank's balanced salt solution, the Detachment Medium For Primate ES Cells (manufactured by ReproCELL) was added, cultured at 37° C. for 10 minutes, and 2 ml of the medium was added to stop the reaction. ..

Article Title: Human pluripotent stem cells induced from undifferentiated stem cells derived from a human postnatal tissue
Article Snippet: .. One hundred μl of the Detachment Medium For Primate ES Cells (manufactured by ReproCELL) was added in the ring and cultured at 37° C. for 10 to 20 minutes. ..

Article Title: Cell culture apparatus and cell culture method using the same
Article Snippet: .. An example of the experiment will be described below. (Cells, Culture Medium, and Reagents Used) Cells: Mouse embryo fibroblasts (ReproCELL Incorporated) and Human iPS cells 201B7 and 253G1 (RIKEN) Culture medium: Medium for primate ES/iPS cells (trade name: Primate ES Cell Medium, ReproCELL Incorporated) Reagents: Recombinant human fibroblast basic growth factor (general name: bFGF, ReproCELL Incorporated), Cell detachment solution for ES/iPS cells (trade name: CTK solution, ReproCELL Incorporated), Phosphate buffered saline (Life Technologies), Cell dissociation solution (trade name: AccuMax, Merk Millipore), Serum-free maintenance medium for human ES/iPS cells (trade name: mTeSR1, STEMCELL TECHNOLOGIES), and Y-27632 (general name for compound, Calbiochem) (Culture Method Using Cell Culture Apparatus) Examples of a method for preparing iPS cells to be cultured in the cell culture apparatus according to the present invention include: (1) inoculation of cell aggregates and (2) inoculation of single cell suspension, and the methods (1) and (2) will be described later. ..

Recombinant:

Article Title: Cell culture apparatus and cell culture method using the same
Article Snippet: .. An example of the experiment will be described below. (Cells, Culture Medium, and Reagents Used) Cells: Mouse embryo fibroblasts (ReproCELL Incorporated) and Human iPS cells 201B7 and 253G1 (RIKEN) Culture medium: Medium for primate ES/iPS cells (trade name: Primate ES Cell Medium, ReproCELL Incorporated) Reagents: Recombinant human fibroblast basic growth factor (general name: bFGF, ReproCELL Incorporated), Cell detachment solution for ES/iPS cells (trade name: CTK solution, ReproCELL Incorporated), Phosphate buffered saline (Life Technologies), Cell dissociation solution (trade name: AccuMax, Merk Millipore), Serum-free maintenance medium for human ES/iPS cells (trade name: mTeSR1, STEMCELL TECHNOLOGIES), and Y-27632 (general name for compound, Calbiochem) (Culture Method Using Cell Culture Apparatus) Examples of a method for preparing iPS cells to be cultured in the cell culture apparatus according to the present invention include: (1) inoculation of cell aggregates and (2) inoculation of single cell suspension, and the methods (1) and (2) will be described later. ..

Saline:

Article Title: Cell culture apparatus and cell culture method using the same
Article Snippet: .. An example of the experiment will be described below. (Cells, Culture Medium, and Reagents Used) Cells: Mouse embryo fibroblasts (ReproCELL Incorporated) and Human iPS cells 201B7 and 253G1 (RIKEN) Culture medium: Medium for primate ES/iPS cells (trade name: Primate ES Cell Medium, ReproCELL Incorporated) Reagents: Recombinant human fibroblast basic growth factor (general name: bFGF, ReproCELL Incorporated), Cell detachment solution for ES/iPS cells (trade name: CTK solution, ReproCELL Incorporated), Phosphate buffered saline (Life Technologies), Cell dissociation solution (trade name: AccuMax, Merk Millipore), Serum-free maintenance medium for human ES/iPS cells (trade name: mTeSR1, STEMCELL TECHNOLOGIES), and Y-27632 (general name for compound, Calbiochem) (Culture Method Using Cell Culture Apparatus) Examples of a method for preparing iPS cells to be cultured in the cell culture apparatus according to the present invention include: (1) inoculation of cell aggregates and (2) inoculation of single cell suspension, and the methods (1) and (2) will be described later. ..

Suspension:

Article Title: Cell culture apparatus and cell culture method using the same
Article Snippet: .. An example of the experiment will be described below. (Cells, Culture Medium, and Reagents Used) Cells: Mouse embryo fibroblasts (ReproCELL Incorporated) and Human iPS cells 201B7 and 253G1 (RIKEN) Culture medium: Medium for primate ES/iPS cells (trade name: Primate ES Cell Medium, ReproCELL Incorporated) Reagents: Recombinant human fibroblast basic growth factor (general name: bFGF, ReproCELL Incorporated), Cell detachment solution for ES/iPS cells (trade name: CTK solution, ReproCELL Incorporated), Phosphate buffered saline (Life Technologies), Cell dissociation solution (trade name: AccuMax, Merk Millipore), Serum-free maintenance medium for human ES/iPS cells (trade name: mTeSR1, STEMCELL TECHNOLOGIES), and Y-27632 (general name for compound, Calbiochem) (Culture Method Using Cell Culture Apparatus) Examples of a method for preparing iPS cells to be cultured in the cell culture apparatus according to the present invention include: (1) inoculation of cell aggregates and (2) inoculation of single cell suspension, and the methods (1) and (2) will be described later. ..

Article Title: Method for inducing differentiation of pluripotent stem cells into cardiomyocytes
Article Snippet: Culture for inducing differentiation in cmES cells was accomplished in a routine manner as follows. cmES cells were washed with PBS and then treated with a commercially available cell dissociation solution for primate ES cells (ReproCELL) at 37° C. for 5 minutes to collect a cell suspension containing cmES cell aggregates. .. Culture for inducing differentiation in cmES cells was accomplished in a routine manner as follows. cmES cells were washed with PBS and then treated with a commercially available cell dissociation solution for primate ES cells (ReproCELL) at 37° C. for 5 minutes to collect a cell suspension containing cmES cell aggregates. .. This non-passed fraction containing cmES cell aggregates was further seeded in a commercially available culture plate with high cell attachment (Primaria; Becton Dickinson) and cultured for 30 minutes, followed by collection of cell aggregates floating in the medium without adhering to the plate.



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Image Search Results


Case 1: Renal angiography and balloon-assisted coil embolization of a right RAVF (A) Baseline right renal angiogram demonstrating a large high-flow RAVF arising from a focally dilated segment of the right renal artery and draining into markedly dilated venous channels, with poor opacification of the renal parenchyma. (B) Angiogram obtained with the balloon catheter inflated in the right renal artery near the shunt showing disappearance of the arteriovenous shunt and improved cortical enhancement via preserved proximal branches, indicating an optimal level for embolization. (C) Final angiogram after balloon-assisted deployment of detachable coils followed by additional pushable coils within the shunt and proximal draining vein, showing complete occlusion of the fistula with preserved antegrade flow into the normal segmental branches. RAVF, renal arteriovenous fistula.

Journal: Radiology Case Reports

Article Title: Balloon-assisted coil embolization for high-flow renal arteriovenous fistula with inferior vena cava dilatation: A report of two cases

doi: 10.1016/j.radcr.2026.04.046

Figure Lengend Snippet: Case 1: Renal angiography and balloon-assisted coil embolization of a right RAVF (A) Baseline right renal angiogram demonstrating a large high-flow RAVF arising from a focally dilated segment of the right renal artery and draining into markedly dilated venous channels, with poor opacification of the renal parenchyma. (B) Angiogram obtained with the balloon catheter inflated in the right renal artery near the shunt showing disappearance of the arteriovenous shunt and improved cortical enhancement via preserved proximal branches, indicating an optimal level for embolization. (C) Final angiogram after balloon-assisted deployment of detachable coils followed by additional pushable coils within the shunt and proximal draining vein, showing complete occlusion of the fistula with preserved antegrade flow into the normal segmental branches. RAVF, renal arteriovenous fistula.

Article Snippet: Detachable coils (Interlock and EMBOLD coils; Boston Scientific Corporation, Marlborough, MA, USA) were first deployed to create a stable frame, and additional pushable coils (C-STOPPER coils; Piolax Medical Devices, Yokohama, Japan; AZUR D-18 coils; Terumo Corporation, Tokyo, Japan; GALAXY G3 and DELTAFILL 18 coils; Cerenovus, Irvine, CA, USA) were then packed within this framework from the venous side toward the arterial side under balloon occlusion, with the aim of increasing the coil filling rate and achieving dense packing.

Techniques: