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Rat Pancreatic Stellate Primary Cells Complete Growth Medium is a primary cells complete growth medium from Innovative Research, supplied as a ready-to-use liquid. More Details: Bacterial detection: Negative Fungal detection: Negative Mycoplasma detection: Negative Endotoxin
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Human Pancreatic Epithelial Primary Cell Culture - T225 Plated Cells Also Avaliable as: Frozen Vial Cells shipped with Dry-ice. Cat#36099-25T25 plated Cells shipped at room temperature. Cat#36099-25-T25 T75 plated Cells shipped at room temperature. Cat#36099-25-T75
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Celprogen Inc
growth media Growth Media, supplied by Celprogen Inc, 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/primary+pancreatic+cells/Human+Pancreatic+Normal+Primary+Cell+Culture+Complete+Growth+Media+with+serum/pmc12358689-82-7-13 Average 93 stars, based on 1 article reviews
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Celprogen Inc
extra cellular matrix Extra Cellular Matrix, supplied by Celprogen Inc, 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/primary+pancreatic+cells/Human+Pancreatic+Normal+Primary+Cell+Culture+Extra-cellular+Matrix/10__1016_slash_j__rbmo__2025__104895-46-19-21 Average 93 stars, based on 1 article reviews
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Celprogen Inc
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DS Pharma Biomedical
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Cell Systems Corporation
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iCell Gene Therapeutics
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Primary Cell Co Ltd
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Celprogen Inc
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Human Pancreatic Type 1 Langerhans Primary Cell Culture - T150 Plated Cells Also Avaliable as: Frozen Vial Cells shipped with Dry-ice. Cat#35001-03 T25 plated Cells shipped at room temperature. Cat#35001-03-T25 T75 plated Cells shipped at
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Image Search Results
Journal: Oncology Letters
Article Title: Anticancer effect of arsenite on cell migration, cell cycle and apoptosis in human pancreatic cancer cells
doi: 10.3892/ol.2016.4564
Figure Lengend Snippet: Effects of PDGF-BB on the migration of AsPC-1 and BxPC-3 pancreatic cancer cells, compared with normal PE cells. (A) AsPC-1, (B) BxPC-3 and (C) PE cells (5×104 cells/well) were treated with the indicated doses of arsenite for 24 h, prior to be seeded in the upper Boyden chamber. Following incubation for 16 h, cells were exposed to 30 ng/ml PDGF-BB for 36 h at 37°C. Cells were then fixed, stained and visualized under a microscope. The average number of migrated cells from five randomly selected fields on the lower surface of the membrane was counted. Data were obtained from ≥3 independent experiments. *P<0.05 vs. controls. Right panels show representative images of the migrated cells stained with clonogenic reagent. PDGF, platelet-derived growth factor; PE, pancreatic epithelial.
Article Snippet:
Techniques: Migration, Incubation, Staining, Microscopy, Membrane, Derivative Assay
Journal: Oncology Letters
Article Title: Anticancer effect of arsenite on cell migration, cell cycle and apoptosis in human pancreatic cancer cells
doi: 10.3892/ol.2016.4564
Figure Lengend Snippet: Effects of arsenite on PARP cleavage in AsPC-1, BxPC-3 and PE cells. (A) AsPC-1, (B) BxPC-3 and (C) PE cells were exposed to arsenite (30 µM) for the indicated time periods. Protein extracts were then harvested and examined by western blotting using anti-PARP and anti-glyceraldehyde-3-phosphate dehydrogenase antibodies. Background-subtracted signal intensity of each protein band was normalized to GAPDH. Data are presented as the mean ± standard deviation of triplicate assay. *P<0.05. PARP, poly(adenosine diphosphate-ribose) polymerase; PE, pancreatic epithelial; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.
Article Snippet:
Techniques: Western Blot, Standard Deviation
Journal: Oncology Letters
Article Title: Anticancer effect of arsenite on cell migration, cell cycle and apoptosis in human pancreatic cancer cells
doi: 10.3892/ol.2016.4564
Figure Lengend Snippet: Effects of arsenite on the phosphorylation of p44/p42 MAPK and Akt in AsPC-1, BxPC-3 and PE cells. (A) AsPC-1, (B) BxPC-3 and (C) PE cells were exposed to arsenite (30 µM) and incubated with 30 ng/ml platelet-derived growth factor-BB for the indicated time periods. Protein extracts were then harvested and examined by western blotting using specific antibodies against phospho-p44/p42 MAPK, p44/p42 MAPK, phospho-Akt and Akt. Background-subtracted signal intensity of each protein band was normalized to Akt. Data are presented as the mean ± standard deviation of triplicate assay. *P<0.05 vs. cells without arsenite exposure. PE, pancreatic epithelial; PDGF, platelet-derived growth factor; phospho, phosphorylated; MAPK, mitogen-activated protein kinase; M, marker.
Article Snippet:
Techniques: Phospho-proteomics, Incubation, Derivative Assay, Western Blot, Standard Deviation, Marker