dna rna protein isolation kit Search Results


dr. p kit-isolation of rna, dna and protein from the same piece of tissue simultaneously  (AMS Biotechnology)
96
AMS Biotechnology dr. p kit-isolation of rna, dna and protein from the same piece of tissue simultaneously
Dr. P Kit Isolation Of Rna, Dna And Protein From The Same Piece Of Tissue Simultaneously, supplied by AMS Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
dr. p kit-isolation of rna, dna and protein from the same piece of tissue simultaneously - by Bioz Stars, 2026-10
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dna rna protein coextraction kit  (tiangen biotech co)
93
tiangen biotech co dna rna protein coextraction kit
Dna Rna Protein Coextraction Kit, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dna+rna+protein+isolation+kit/DNA%2FRNA%2FProtein+Isolation+Kit/pmc07308808-80-22-26
Average 93 stars, based on 1 article reviews
dna rna protein coextraction kit - by Bioz Stars, 2026-10
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tianprep dna rna protein isolation kit  (tiangen biotech co)
94
tiangen biotech co tianprep dna rna protein isolation kit
Tianprep Dna Rna Protein Isolation Kit, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
tianprep dna rna protein isolation kit - by Bioz Stars, 2026-10
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dr p kit-isolation of rna, dna, and protein from the same piece of tissue simultaneously  (BioChain Institute)
90
BioChain Institute dr p kit-isolation of rna, dna, and protein from the same piece of tissue simultaneously
Adhesion of pancreatic islets to fibronectin motif. (A) The islets (total of 250 IEQ/well) were seeded onto six-well plates chemically coated with a fibronectin motif (non-coated plate: control). The CDSD-500 has a dot size of 500 μm. The CDSD-1500 has a dot size of 1,500 μm. For comparison, a plate (CDS plate) in which the surface treatment of the dots was performed on the entire bottom surface of the well was used. Photographs of islet cells taken by optical microscope at 1 week after seeding on each plate are shown. Scale bar = 500 μm. (B) <t>DNA</t> <t>was</t> <t>extracted/purified</t> from the adherent islets, and the DNA concentration was measured ( n = 4; control, n = 1). The data are presented as the mean ± SE (standard error of the mean). * P < 0.05. (C) The expression of integrins α1, α2, α3, α5, α6, αV, β1, β3, β5, β6, and β8 in islets ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples. (D) The expression of cadherins 1, 2, 3, 5, 6, 7, 10, 11, 12, 18, 19, and 22 in islets ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples.
Dr P Kit Isolation Of Rna, Dna, And Protein From The Same Piece Of Tissue Simultaneously, supplied by BioChain Institute, 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/dna+rna+protein+isolation+kit/dr+p+kit+isolation+of+rna++dna++and+protein+from+the+same+piece+of+tissue+simultaneously/pmc09449504-53-11-21
Average 90 stars, based on 1 article reviews
dr p kit-isolation of rna, dna, and protein from the same piece of tissue simultaneously - by Bioz Stars, 2026-10
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Image Search Results


Adhesion of pancreatic islets to fibronectin motif. (A) The islets (total of 250 IEQ/well) were seeded onto six-well plates chemically coated with a fibronectin motif (non-coated plate: control). The CDSD-500 has a dot size of 500 μm. The CDSD-1500 has a dot size of 1,500 μm. For comparison, a plate (CDS plate) in which the surface treatment of the dots was performed on the entire bottom surface of the well was used. Photographs of islet cells taken by optical microscope at 1 week after seeding on each plate are shown. Scale bar = 500 μm. (B) DNA was extracted/purified from the adherent islets, and the DNA concentration was measured ( n = 4; control, n = 1). The data are presented as the mean ± SE (standard error of the mean). * P < 0.05. (C) The expression of integrins α1, α2, α3, α5, α6, αV, β1, β3, β5, β6, and β8 in islets ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples. (D) The expression of cadherins 1, 2, 3, 5, 6, 7, 10, 11, 12, 18, 19, and 22 in islets ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples.

Journal: Cell Transplantation

Article Title: Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold

doi: 10.1177/09636897221120500

Figure Lengend Snippet: Adhesion of pancreatic islets to fibronectin motif. (A) The islets (total of 250 IEQ/well) were seeded onto six-well plates chemically coated with a fibronectin motif (non-coated plate: control). The CDSD-500 has a dot size of 500 μm. The CDSD-1500 has a dot size of 1,500 μm. For comparison, a plate (CDS plate) in which the surface treatment of the dots was performed on the entire bottom surface of the well was used. Photographs of islet cells taken by optical microscope at 1 week after seeding on each plate are shown. Scale bar = 500 μm. (B) DNA was extracted/purified from the adherent islets, and the DNA concentration was measured ( n = 4; control, n = 1). The data are presented as the mean ± SE (standard error of the mean). * P < 0.05. (C) The expression of integrins α1, α2, α3, α5, α6, αV, β1, β3, β5, β6, and β8 in islets ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples. (D) The expression of cadherins 1, 2, 3, 5, 6, 7, 10, 11, 12, 18, 19, and 22 in islets ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples.

Article Snippet: DNA was extracted/purified carried out using Dr P Kit-Isolation of RNA, DNA, and Protein from the same piece of tissue simultaneously (BioChain Institute Inc., Newark, CA, USA) from the adherent islets, duct epithelial cells, and acinar cells, and DNA concentrations were measured using NanoDrop One/One c (Thermo Fisher Scientific, Tokyo, Japan).

Techniques: Control, Comparison, Microscopy, Purification, Concentration Assay, Expressing

Adhesion of duct epithelial cells to fibronectin motif. (A) The duct epithelial cells (total of 25 aggregates/well) were seeded onto six-well plates chemically coated with a fibronectin motif (non-coated plate: control). The CDSD-500 has a dot size of 500 μm. The CDSD-1500 has a dot size of 1,500 μm. For comparison, a plate (CDS plate) in which the surface treatment of the dots was performed on the entire bottom surface of the well was used. Photographs of duct epithelial cells taken by optical microscope at 1 week after seeding on each plate are shown. Scale bar = 500 μm. (B) DNA was extracted/purified from the adherent duct epithelial cells, and the DNA concentration was measured ( n = 2). The data are presented as the mean ± SE (standard error of the mean). * P < 0.05. (C) The expression of integrins α1, α2, α6, αV, β1, β5, β6, and β8 in duct epithelial cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples. (D) The expression of cadherin 1, 2, 3, 6, 7, 10, 11, and 12 in duct epithelial cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples.

Journal: Cell Transplantation

Article Title: Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold

doi: 10.1177/09636897221120500

Figure Lengend Snippet: Adhesion of duct epithelial cells to fibronectin motif. (A) The duct epithelial cells (total of 25 aggregates/well) were seeded onto six-well plates chemically coated with a fibronectin motif (non-coated plate: control). The CDSD-500 has a dot size of 500 μm. The CDSD-1500 has a dot size of 1,500 μm. For comparison, a plate (CDS plate) in which the surface treatment of the dots was performed on the entire bottom surface of the well was used. Photographs of duct epithelial cells taken by optical microscope at 1 week after seeding on each plate are shown. Scale bar = 500 μm. (B) DNA was extracted/purified from the adherent duct epithelial cells, and the DNA concentration was measured ( n = 2). The data are presented as the mean ± SE (standard error of the mean). * P < 0.05. (C) The expression of integrins α1, α2, α6, αV, β1, β5, β6, and β8 in duct epithelial cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples. (D) The expression of cadherin 1, 2, 3, 6, 7, 10, 11, and 12 in duct epithelial cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples.

Article Snippet: DNA was extracted/purified carried out using Dr P Kit-Isolation of RNA, DNA, and Protein from the same piece of tissue simultaneously (BioChain Institute Inc., Newark, CA, USA) from the adherent islets, duct epithelial cells, and acinar cells, and DNA concentrations were measured using NanoDrop One/One c (Thermo Fisher Scientific, Tokyo, Japan).

Techniques: Control, Comparison, Microscopy, Purification, Concentration Assay, Expressing

Adhesion of acinar cells to fibronectin motif. (A) The acinar cells (total of 1.5–3 × 10 6 cells/well) were seeded onto six-well plates chemically coated with a fibronectin motif (non-coated plate: control). The CDSD-500 has a dot size of 500 μm. The CDSD-1500 has a dot size of 1,500 μm. For comparison, a plate (CDS plate) in which the surface treatment of the dots was performed on the entire bottom surface of the well was used. Photographs of acinar cells taken by optical microscope at 1 week after seeding on each plate are shown. Scale bar = 500 μm. (B) DNA was extracted/purified from the adherent acinar cells, and the DNA concentration was measured ( n = 2). The data are presented as the mean ± SE (standard error of the mean). * P < 0.05. (C) The expression of integrins α4, α6, α8, αV, β3, β5, β6, β7, and β8 in acinar cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples. (D) The expression of cadherin 1, 4, 6, 7, 9, 11, 12, 19, 22, and 24 in acinar cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples.

Journal: Cell Transplantation

Article Title: Adhesion Characteristics of Human Pancreatic Islets, Duct Epithelial Cells, and Acinar Cells to a Polymer Scaffold

doi: 10.1177/09636897221120500

Figure Lengend Snippet: Adhesion of acinar cells to fibronectin motif. (A) The acinar cells (total of 1.5–3 × 10 6 cells/well) were seeded onto six-well plates chemically coated with a fibronectin motif (non-coated plate: control). The CDSD-500 has a dot size of 500 μm. The CDSD-1500 has a dot size of 1,500 μm. For comparison, a plate (CDS plate) in which the surface treatment of the dots was performed on the entire bottom surface of the well was used. Photographs of acinar cells taken by optical microscope at 1 week after seeding on each plate are shown. Scale bar = 500 μm. (B) DNA was extracted/purified from the adherent acinar cells, and the DNA concentration was measured ( n = 2). The data are presented as the mean ± SE (standard error of the mean). * P < 0.05. (C) The expression of integrins α4, α6, α8, αV, β3, β5, β6, β7, and β8 in acinar cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples. (D) The expression of cadherin 1, 4, 6, 7, 9, 11, 12, 19, 22, and 24 in acinar cells ( n = 1). β-actin housekeeping genes were used as denominators for comparing samples.

Article Snippet: DNA was extracted/purified carried out using Dr P Kit-Isolation of RNA, DNA, and Protein from the same piece of tissue simultaneously (BioChain Institute Inc., Newark, CA, USA) from the adherent islets, duct epithelial cells, and acinar cells, and DNA concentrations were measured using NanoDrop One/One c (Thermo Fisher Scientific, Tokyo, Japan).

Techniques: Control, Comparison, Microscopy, Purification, Concentration Assay, Expressing