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hair papilla cell growth medium  (PromoCell)


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    PromoCell hair papilla cell growth medium
    Hair Papilla Cell Growth Medium, supplied by PromoCell, used in various techniques. Bioz Stars score: 95/100, based on 105 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/follicle+dermal+papilla+cell+growth+medium/Follicle+Dermal+Papilla+Cell+Growth+Medium/us12648794-41-21-29
    Average 95 stars, based on 105 article reviews
    hair papilla cell growth medium - by Bioz Stars, 2026-09
    95/100 stars

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    Related Articles

    Cell Culture:

    Article Title: Hydrogel-Based Extracellular Vesicle Isolation Method from Various Biological Solutions.
    Article Snippet: .. The human follicle dermal papilla cells cell line was cultured at 37 °C in a humidified atmosphere containing 5% CO2 in Follicle Dermal Papilla Cell Growth Medium (C-26501, Promo Cell). ..

    Article Title: Age-related downregulation of dihydrotestosterone-inactivating enzymes in human scalp sebaceous glands
    Article Snippet: SEB-1 male-derived immortalized sebocyte cells were kindly provided by the Penn State Research Foundation and cultured in Reduced Serum DMEM/Ham's F-12 Medium (Nacalai Tesque) supplemented with 5% fetal bovine serum, 180 μM adenine, 0.4 μg/ml hydrocortisone, 10 ng/ml epidermal growth factor, and 10 μM isoproterenol. .. Human DPCs, derived from the temple region of a 53-year-old Caucasian male, were obtained (c-12071, PromoCell) and cultured in Follicle Dermal Papilla Cell Growth Medium (Ready-to-use) (c-26501, PromoCell). ..

    Article Title: Poly-D,L-Lactic Acid Filler Restores Hair Thickness and Shine by Ameliorating Age-Associated Follicular Decline
    Article Snippet: .. Cell Culture Human DPCs (hDPCs) were purchased from PromoCell GmbH (Heidelberg, Germany) and cultured in Follicle Dermal Papilla Cell Growth Medium (PromoCell) supplemented with the provided growth supplement mix and 1% penicillin/streptomycin, in accordance with the manufacturer’s instructions. .. Human HFKs (hHFKs) were obtained from ScienCell Research Laboratories (Carlsbad, CA, USA) and maintained in Keratinocyte Medium (ScienCell Research Laboratories) supplemented with keratinocyte growth supplement and 1% penicillin/streptomycin.

    Article Title: Poly-D,L-Lactic Acid Filler Restores Hair Thickness and Shine by Ameliorating Age-Associated Follicular Decline
    Article Snippet: .. Human DPCs (hDPCs) were purchased from PromoCell GmbH (Heidelberg, Germany) and cultured in Follicle Dermal Papilla Cell Growth Medium (PromoCell) supplemented with the provided growth supplement mix and 1% penicillin/streptomycin, in accordance with the manufacturer’s instructions. .. Human HFKs (hHFKs) were obtained from ScienCell Research Laboratories (Carlsbad, CA, USA) and maintained in Keratinocyte Medium (ScienCell Research Laboratories) supplemented with keratinocyte growth supplement and 1% penicillin/streptomycin.

    Article Title: Age-related downregulation of dihydrotestosterone-inactivating enzymes in human scalp sebaceous glands.
    Article Snippet: SEB-1 male-derived immortalized sebocyte cells were kindly provided by the Penn State Research Foundation and cultured in Reduced Serum DMEM/Ham's F-12 Medium (Nacalai Tesque) supplemented with 5% fetal bovine serum, 180 μM adenine, 0.4 μg/ml hydrocortisone, 10 ng/ml epidermal growth factor, and 10 μM isoproterenol. .. Human DPCs, derived from the temple region of a 53-year-old Caucasian male, were obtained (c-12071, PromoCell) and cultured in Follicle Dermal Papilla Cell Growth Medium (Ready-to-use) (c-26501, PromoCell). ..

    Article Title: Anti-Hair Loss Activity of Healthy Human Scalp-Derived Staphylococcus capitis KMH304 Ferment Filtrate in Human Hair-Follicle Dermal Papilla and Keratinocyte Cells
    Article Snippet: .. HFDPCs (C-12071; Promocell, Heidelberg, Germany) were cultured in Follicle Dermal Papilla Cell Growth Medium (C-26501; Promocell) supplemented with 1% antibiotic–antimycotic (Gibco; Thermo Fisher Scientific, Waltham, MA, USA). .. For the in vitro experiments, cells were seeded in Dulbecco’s modified Eagle’s medium (DMEM; SH 30243.01; Hyclone, Logan, UT, USA) supplemented with 5% fetal bovine serum (FBS; 16000-044; Gibco; Thermo Fisher Scientific) and 1% antibiotic–antimycotic (15240-062; Gibco; Thermo Fisher Scientific) [ ].

    Article Title: Ageratum houstonianum Extract and Agerarin Promote Hair Growth via MAPK/AP-1 Axis-Dependent Upregulation of SCUBE3 in Human Dermal Papilla Cells
    Article Snippet: .. Primary HFDP cells isolated from human dermis of the scalp were purchased from PromoCell (Heidelberg, Germany) and cultured in Follicle Dermal Papilla Cell Growth medium (PromoCell) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 μg/mL streptomycin at 37 °C in a humidified atmosphere of 5% CO 2 . ..

    Derivative Assay:

    Article Title: Age-related downregulation of dihydrotestosterone-inactivating enzymes in human scalp sebaceous glands
    Article Snippet: SEB-1 male-derived immortalized sebocyte cells were kindly provided by the Penn State Research Foundation and cultured in Reduced Serum DMEM/Ham's F-12 Medium (Nacalai Tesque) supplemented with 5% fetal bovine serum, 180 μM adenine, 0.4 μg/ml hydrocortisone, 10 ng/ml epidermal growth factor, and 10 μM isoproterenol. .. Human DPCs, derived from the temple region of a 53-year-old Caucasian male, were obtained (c-12071, PromoCell) and cultured in Follicle Dermal Papilla Cell Growth Medium (Ready-to-use) (c-26501, PromoCell). ..

    Article Title: Age-related downregulation of dihydrotestosterone-inactivating enzymes in human scalp sebaceous glands.
    Article Snippet: SEB-1 male-derived immortalized sebocyte cells were kindly provided by the Penn State Research Foundation and cultured in Reduced Serum DMEM/Ham's F-12 Medium (Nacalai Tesque) supplemented with 5% fetal bovine serum, 180 μM adenine, 0.4 μg/ml hydrocortisone, 10 ng/ml epidermal growth factor, and 10 μM isoproterenol. .. Human DPCs, derived from the temple region of a 53-year-old Caucasian male, were obtained (c-12071, PromoCell) and cultured in Follicle Dermal Papilla Cell Growth Medium (Ready-to-use) (c-26501, PromoCell). ..

    Isolation:

    Article Title: Ageratum houstonianum Extract and Agerarin Promote Hair Growth via MAPK/AP-1 Axis-Dependent Upregulation of SCUBE3 in Human Dermal Papilla Cells
    Article Snippet: .. Primary HFDP cells isolated from human dermis of the scalp were purchased from PromoCell (Heidelberg, Germany) and cultured in Follicle Dermal Papilla Cell Growth medium (PromoCell) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 μg/mL streptomycin at 37 °C in a humidified atmosphere of 5% CO 2 . ..



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    Screening process to determine peptides with hair-restoring properties. ( A ) <t>Human</t> <t>Follicle</t> <t>Dermal</t> <t>Papilla</t> <t>Cell</t> (HFDPCs) viability of over 200 cell-penetrating peptides, with EGF as the positive control. The red dots mark the peptides with the highest cell viability. ( B ) Western Blot results showing the upregulation of β-catenin and p-ERK proteins of 22 chosen peptides compared to the control. Peptide No.218 (in red rectangle) showed the highest expression level of β-catenin and p-ERK proteins, and was chosen for subsequent analyses. ( C ) Cell-penetrating capability of DualPep-ALO was evaluated using FITC-conjugated peptides in HFDPCs. Cells were treated with FITC-DualPep-ALO or FITC-TAT (2.5 µM, 2 h), followed by extensive washing and trypsinization to remove membrane-bound peptides. Intracellular fluorescence intensity was quantified by flow cytometry. Each experiment was performed three times
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    Image Search Results


    Screening process to determine peptides with hair-restoring properties. ( A ) Human Follicle Dermal Papilla Cell (HFDPCs) viability of over 200 cell-penetrating peptides, with EGF as the positive control. The red dots mark the peptides with the highest cell viability. ( B ) Western Blot results showing the upregulation of β-catenin and p-ERK proteins of 22 chosen peptides compared to the control. Peptide No.218 (in red rectangle) showed the highest expression level of β-catenin and p-ERK proteins, and was chosen for subsequent analyses. ( C ) Cell-penetrating capability of DualPep-ALO was evaluated using FITC-conjugated peptides in HFDPCs. Cells were treated with FITC-DualPep-ALO or FITC-TAT (2.5 µM, 2 h), followed by extensive washing and trypsinization to remove membrane-bound peptides. Intracellular fluorescence intensity was quantified by flow cytometry. Each experiment was performed three times

    Journal: BMC Biotechnology

    Article Title: A novel cell-penetrating peptide supports hair follicle growth through anti-inflammatory and growth factor–associated mechanisms in preclinical models

    doi: 10.1186/s12896-026-01130-4

    Figure Lengend Snippet: Screening process to determine peptides with hair-restoring properties. ( A ) Human Follicle Dermal Papilla Cell (HFDPCs) viability of over 200 cell-penetrating peptides, with EGF as the positive control. The red dots mark the peptides with the highest cell viability. ( B ) Western Blot results showing the upregulation of β-catenin and p-ERK proteins of 22 chosen peptides compared to the control. Peptide No.218 (in red rectangle) showed the highest expression level of β-catenin and p-ERK proteins, and was chosen for subsequent analyses. ( C ) Cell-penetrating capability of DualPep-ALO was evaluated using FITC-conjugated peptides in HFDPCs. Cells were treated with FITC-DualPep-ALO or FITC-TAT (2.5 µM, 2 h), followed by extensive washing and trypsinization to remove membrane-bound peptides. Intracellular fluorescence intensity was quantified by flow cytometry. Each experiment was performed three times

    Article Snippet: HFDPCs were cultured in Human Follicle Dermal Papilla Cell Growth Medium (PromoCell, Heidelberg, Germany) supplemented with fetal calf serum, bovine pituitary extract, basic fibroblast growth factor, and insulin.

    Techniques: Positive Control, Western Blot, Control, Expressing, Membrane, Fluorescence, Flow Cytometry

    Effects of DualPep-ALO on cell viability. ( A ) Mouse macrophage viability after 24-hour treatment with various concentrations of DualPep-ALO (0.64, 3.2, 16, 80 µM), compared with L-NMMA (25 µM). ( B ) Human Follicle Dermal Papilla Cells viability after treatment with DualPep-ALO (3.2, 16, 80 µM) for 24, 48, and 72 hours, compared with minoxidil (20 µM). Data are presented as mean ± SD. *p < 0.05 vs. negative control at the same time point. Each experiment was performed three times

    Journal: BMC Biotechnology

    Article Title: A novel cell-penetrating peptide supports hair follicle growth through anti-inflammatory and growth factor–associated mechanisms in preclinical models

    doi: 10.1186/s12896-026-01130-4

    Figure Lengend Snippet: Effects of DualPep-ALO on cell viability. ( A ) Mouse macrophage viability after 24-hour treatment with various concentrations of DualPep-ALO (0.64, 3.2, 16, 80 µM), compared with L-NMMA (25 µM). ( B ) Human Follicle Dermal Papilla Cells viability after treatment with DualPep-ALO (3.2, 16, 80 µM) for 24, 48, and 72 hours, compared with minoxidil (20 µM). Data are presented as mean ± SD. *p < 0.05 vs. negative control at the same time point. Each experiment was performed three times

    Article Snippet: HFDPCs were cultured in Human Follicle Dermal Papilla Cell Growth Medium (PromoCell, Heidelberg, Germany) supplemented with fetal calf serum, bovine pituitary extract, basic fibroblast growth factor, and insulin.

    Techniques: Negative Control

    Antioxidant enzyme activities in Human Follicle Dermal Papilla Cells (HFPDCs) treated with DualPep-ALO. DualPep-ALO (3.2, 16, 80 µM) enhanced the activities of ( A ) Superoxide dismutase (SOD) and ( B ) catalase (CAT) in HFPDCs after oxidative stress induction with H 2 O 2 (400 µM). L-Ascorbic acid (100 µM) was used as a positive control. Data are expressed as mean ± SD. *p < 0.05 vs. negative control; #p < 0.05 vs. H 2 O 2 -treated group. Each experiment was performed three times

    Journal: BMC Biotechnology

    Article Title: A novel cell-penetrating peptide supports hair follicle growth through anti-inflammatory and growth factor–associated mechanisms in preclinical models

    doi: 10.1186/s12896-026-01130-4

    Figure Lengend Snippet: Antioxidant enzyme activities in Human Follicle Dermal Papilla Cells (HFPDCs) treated with DualPep-ALO. DualPep-ALO (3.2, 16, 80 µM) enhanced the activities of ( A ) Superoxide dismutase (SOD) and ( B ) catalase (CAT) in HFPDCs after oxidative stress induction with H 2 O 2 (400 µM). L-Ascorbic acid (100 µM) was used as a positive control. Data are expressed as mean ± SD. *p < 0.05 vs. negative control; #p < 0.05 vs. H 2 O 2 -treated group. Each experiment was performed three times

    Article Snippet: HFDPCs were cultured in Human Follicle Dermal Papilla Cell Growth Medium (PromoCell, Heidelberg, Germany) supplemented with fetal calf serum, bovine pituitary extract, basic fibroblast growth factor, and insulin.

    Techniques: Positive Control, Negative Control