primary rat dermal fibroblasts Search Results


rat dermal fibroblast primary cells complete growth medium  (Innovative Research Inc)
N/A
Rat Dermal Fibroblast 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 primary dermal fibroblast containing disc of rat-tail collagen type i  (Corning Life Sciences)
90
Corning Life Sciences human primary dermal fibroblast containing disc of rat-tail collagen type i
Organotypic cultures (OTCs) of keratinocyte cell lines. HaCaT ( A ), N/Tert-1 ( B ), KEB-11 ( C ) and NEB-1 ( D ) cells were co-cultured with primary dermal <t>fibroblasts</t> in OTCs for 7 and 9 days, followed by paraffin embedding and sectioning. Images of H&E-stained specimens were acquired using Leica Epi DM5000B or Nikon Eclipse 80i microscopes; scale bar = 200 μm.
Human Primary Dermal Fibroblast Containing Disc Of Rat Tail Collagen Type I, supplied by Corning Life Sciences, 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/primary+rat+dermal+fibroblasts/human+primary+dermal+fibroblast+containing+disc+of+rat+tail+collagen+type+i/pmc06374370-184-11-21
Average 90 stars, based on 1 article reviews
human primary dermal fibroblast containing disc of rat-tail collagen type i - by Bioz Stars, 2026-10
90/100 stars
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primary rat dermal fibroblasts  (PELOBIOTECH GmbH)
90
PELOBIOTECH GmbH primary rat dermal fibroblasts
A , Rat dermal <t>fibroblasts</t> (RDF) and B , human dermal fibroblasts (HDF) were treated with 10 ng/ml hLIF, hOSM, mOSM or rOSM for 15 min. The phosphorylation levels of STAT1, STAT3, ERK1/2 as well as STAT5, p38 and Akt were detected via Western blot analysis. The blots were stripped and reprobed with antibodies recognizing the proteins irrespective of their activation status. Additionally an α-tubulin loading control was included. Phosphorylation intensities were quantified by chemiluminescence analysis and normalized to tubulin. Activation determined for rOSM was set to 100%. Shown are the means (n = 3) with standard error of mean (SEM). * p<0.05, ** p<0.01, *** p<0.001 untreated vs. cytokine-treated sample.
Primary Rat Dermal Fibroblasts, supplied by PELOBIOTECH GmbH, 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/primary+rat+dermal+fibroblasts/primary+rat+dermal+fibroblasts/pmc03425591-157-0-7
Average 90 stars, based on 1 article reviews
primary rat dermal fibroblasts - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


Organotypic cultures (OTCs) of keratinocyte cell lines. HaCaT ( A ), N/Tert-1 ( B ), KEB-11 ( C ) and NEB-1 ( D ) cells were co-cultured with primary dermal fibroblasts in OTCs for 7 and 9 days, followed by paraffin embedding and sectioning. Images of H&E-stained specimens were acquired using Leica Epi DM5000B or Nikon Eclipse 80i microscopes; scale bar = 200 μm.

Journal: Scientific Reports

Article Title: The monoclonal antibody EPR1614Y against the stem cell biomarker keratin K15 lacks specificity and reacts with other keratins

doi: 10.1038/s41598-018-38163-5

Figure Lengend Snippet: Organotypic cultures (OTCs) of keratinocyte cell lines. HaCaT ( A ), N/Tert-1 ( B ), KEB-11 ( C ) and NEB-1 ( D ) cells were co-cultured with primary dermal fibroblasts in OTCs for 7 and 9 days, followed by paraffin embedding and sectioning. Images of H&E-stained specimens were acquired using Leica Epi DM5000B or Nikon Eclipse 80i microscopes; scale bar = 200 μm.

Article Snippet: HaCaT, N/Tert-1, KEB-11 and NEB-1 keratinocytes were seeded on a human primary dermal fibroblast containing disc of rat-tail collagen type I (Corning, UK) in a Millipore ® Millicell ® (Sigma-Aldrich, UK).

Techniques: Cell Culture, Staining

A , Rat dermal fibroblasts (RDF) and B , human dermal fibroblasts (HDF) were treated with 10 ng/ml hLIF, hOSM, mOSM or rOSM for 15 min. The phosphorylation levels of STAT1, STAT3, ERK1/2 as well as STAT5, p38 and Akt were detected via Western blot analysis. The blots were stripped and reprobed with antibodies recognizing the proteins irrespective of their activation status. Additionally an α-tubulin loading control was included. Phosphorylation intensities were quantified by chemiluminescence analysis and normalized to tubulin. Activation determined for rOSM was set to 100%. Shown are the means (n = 3) with standard error of mean (SEM). * p<0.05, ** p<0.01, *** p<0.001 untreated vs. cytokine-treated sample.

Journal: PLoS ONE

Article Title: Characterization of the Rat Oncostatin M Receptor Complex Which Resembles the Human, but Differs from the Murine Cytokine Receptor

doi: 10.1371/journal.pone.0043155

Figure Lengend Snippet: A , Rat dermal fibroblasts (RDF) and B , human dermal fibroblasts (HDF) were treated with 10 ng/ml hLIF, hOSM, mOSM or rOSM for 15 min. The phosphorylation levels of STAT1, STAT3, ERK1/2 as well as STAT5, p38 and Akt were detected via Western blot analysis. The blots were stripped and reprobed with antibodies recognizing the proteins irrespective of their activation status. Additionally an α-tubulin loading control was included. Phosphorylation intensities were quantified by chemiluminescence analysis and normalized to tubulin. Activation determined for rOSM was set to 100%. Shown are the means (n = 3) with standard error of mean (SEM). * p<0.05, ** p<0.01, *** p<0.001 untreated vs. cytokine-treated sample.

Article Snippet: Primary rat dermal fibroblasts were obtained from PELOBiotech (Martinsried, Germany).

Techniques: Phospho-proteomics, Western Blot, Activation Assay, Control