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follicle dermal papilla cell basal medium  (PromoCell)


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    PromoCell follicle dermal papilla cell basal medium
    Follicle Dermal Papilla Cell Basal Medium, supplied by PromoCell, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/follicle+dermal+papilla+cell+basal+medium/Follicle+Dermal+Papilla+Cell+Basal+Medium/pm41922417-247-8-14
    Average 92 stars, based on 4 article reviews
    follicle dermal papilla cell basal medium - by Bioz Stars, 2026-09
    92/100 stars

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    Related Articles

    Recombinant:

    Article Title: Extracellular Signal-Regulated Kinase Mediates Ebastine-Induced Human Follicle Dermal Papilla Cell Proliferation
    Article Snippet: HFDPC were purchased from PromoCell (Heidelberg, Germany). .. The cells were maintained in follicle dermal papilla cell basal medium supplemented with 4% fetal calf serum, 0.4% bovine pituitary extract, 1 ng/mL basic fibroblast growth factor, and 5 μ g/mL recombinant human insulin (PromoCell) at 37°C in 5% CO 2 . .. Alkaline phosphatase activity was assessed by a biochemical colorimetric assay using an alkaline phosphatase assay kit (GeneTex Inc., Irvine, CA, USA).

    Article Title: Malus pumila Mill. cv Annurca apple extract might be therapeutically useful against oxidative stress and patterned hair loss.
    Article Snippet: .. Cell culture and sample preparation Human hair follicle dermal papilla cells (HFDPCSs) were purchased from PromoCell (Heidelberg, Germany) and maintained in a follicle dermal papilla cell basal medium supplemented, according to the company, with fetal calf serum (4%), bovine pituitary extract (0.4%), basic fibroblast growth factor (FGF) (1 ng mL 1) and recombinant human insulin (5 lg mL 1) at 37 °C in a humidified atmosphere of 5% CO2. ..

    Incubation:

    Article Title: Efficacy of Asymmetric siRNA Targeting Androgen Receptors for the Treatment of Androgenetic Alopecia.
    Article Snippet: Asymmetric small interfering RNAs (asiRNAs) that mediate RNA interference have been investigated for therapeutic use in various tissues, including skin tissue.. Androgenetic alopecia (AGA) is caused by a combination of genetic factors, resulting in sensitivity to dihydrotestosterone (DHT), which binds to the androgen receptor (AR) to mediate a series of biomolecular changes leading to hair loss.. This study aimed to evaluate the therapeutic potential of a cell-penetrating, AR-targeting asiRNA (cp-asiAR) for AGA treatment, which was designed to silence the AR gene.

    Cell Culture:

    Article Title: Malus pumila Mill. cv Annurca apple extract might be therapeutically useful against oxidative stress and patterned hair loss.
    Article Snippet: .. Cell culture and sample preparation Human hair follicle dermal papilla cells (HFDPCSs) were purchased from PromoCell (Heidelberg, Germany) and maintained in a follicle dermal papilla cell basal medium supplemented, according to the company, with fetal calf serum (4%), bovine pituitary extract (0.4%), basic fibroblast growth factor (FGF) (1 ng mL 1) and recombinant human insulin (5 lg mL 1) at 37 °C in a humidified atmosphere of 5% CO2. ..

    Sample Prep:

    Article Title: Malus pumila Mill. cv Annurca apple extract might be therapeutically useful against oxidative stress and patterned hair loss.
    Article Snippet: .. Cell culture and sample preparation Human hair follicle dermal papilla cells (HFDPCSs) were purchased from PromoCell (Heidelberg, Germany) and maintained in a follicle dermal papilla cell basal medium supplemented, according to the company, with fetal calf serum (4%), bovine pituitary extract (0.4%), basic fibroblast growth factor (FGF) (1 ng mL 1) and recombinant human insulin (5 lg mL 1) at 37 °C in a humidified atmosphere of 5% CO2. ..



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    Fig. 8. Detection of nuclear translocation of Androgen receptor with Azami green fluorescence tang after the testosterone treatment of 100 nM. H2B_0h indicates the cell images obtained <t>from</t> <t>DPCs</t> which only expresses mStrawberry-labeled H2B just after the ligand stimulation. No green fluorescence. Clone 7_0h indicates the cell images obtained from the <t>DPC</t> of clone 7, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 10_0h indicates the cell images obtained from the DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 7_1h indicates the cell images obtained from DPC of clone 7, which expresses mStrawberry-labeled H2B, and Azami green-tagged AR at 1 hour after the ligand stimulation. Clone 10_1h indicates the cell images obtained from DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR at 1 hour after the ligand stimulation.
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    Fig. 8. Detection of nuclear translocation of Androgen receptor with Azami green fluorescence tang after the testosterone treatment of 100 nM. H2B_0h indicates the cell images obtained <t>from</t> <t>DPCs</t> which only expresses mStrawberry-labeled H2B just after the ligand stimulation. No green fluorescence. Clone 7_0h indicates the cell images obtained from the <t>DPC</t> of clone 7, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 10_0h indicates the cell images obtained from the DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 7_1h indicates the cell images obtained from DPC of clone 7, which expresses mStrawberry-labeled H2B, and Azami green-tagged AR at 1 hour after the ligand stimulation. Clone 10_1h indicates the cell images obtained from DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR at 1 hour after the ligand stimulation.
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    Image Search Results


    Fig. 8. Detection of nuclear translocation of Androgen receptor with Azami green fluorescence tang after the testosterone treatment of 100 nM. H2B_0h indicates the cell images obtained from DPCs which only expresses mStrawberry-labeled H2B just after the ligand stimulation. No green fluorescence. Clone 7_0h indicates the cell images obtained from the DPC of clone 7, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 10_0h indicates the cell images obtained from the DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 7_1h indicates the cell images obtained from DPC of clone 7, which expresses mStrawberry-labeled H2B, and Azami green-tagged AR at 1 hour after the ligand stimulation. Clone 10_1h indicates the cell images obtained from DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR at 1 hour after the ligand stimulation.

    Journal: Tissue & cell

    Article Title: Detection of the nuclear translocation of androgen receptor using quantitative and automatic cell imaging analysis.

    doi: 10.1016/j.tice.2024.102631

    Figure Lengend Snippet: Fig. 8. Detection of nuclear translocation of Androgen receptor with Azami green fluorescence tang after the testosterone treatment of 100 nM. H2B_0h indicates the cell images obtained from DPCs which only expresses mStrawberry-labeled H2B just after the ligand stimulation. No green fluorescence. Clone 7_0h indicates the cell images obtained from the DPC of clone 7, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 10_0h indicates the cell images obtained from the DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR just after the ligand stimulation. Clone 7_1h indicates the cell images obtained from DPC of clone 7, which expresses mStrawberry-labeled H2B, and Azami green-tagged AR at 1 hour after the ligand stimulation. Clone 10_1h indicates the cell images obtained from DPC of clone 10, which expresses mStrawberry-labeled H2B and Azami green-tagged AR at 1 hour after the ligand stimulation.

    Article Snippet: DPCs were cultured in a follicle DPC medium (cat. no. C-26500, PromoCell,) with a supplement pack (cat. no. C-39620, PromoCell).

    Techniques: Translocation Assay, Fluorescence, Labeling