human primary dermal fibroblast cell line hdf α Search Results


human primary dermal fibroblast cell line hdf α  (ScienCell)
90
ScienCell human primary dermal fibroblast cell line hdf α
The effect of S. frutescens extract on the viability of (a) A375 melanoma, (b) Colo-800 melanoma, (c) HDF α <t>fibroblast,</t> and (d) Hek 293 cells after 24, 48, and 72 h of treatment. The viability was assessed using the alamarBlue assay and expressed as percentage relative to the control-treated cells (0 mg/mL). Error bars represent the SEM ( n ≥ 3) and ∗ indicates a significant difference from 0 mg/mL ( P < 0.05).
Human Primary Dermal Fibroblast Cell Line Hdf α, supplied by ScienCell, 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/human+primary+dermal+fibroblast+cell+line+hdf+%CE%B1/human+dermal+fibroblasts++hdfs+/pmc05021500-28-2-13
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human primary dermal fibroblast cell line hdf α - by Bioz Stars, 2026-09
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normal human dermal fibroblast alpha cells  (ATCC)
99
ATCC normal human dermal fibroblast alpha cells
The effect of S. frutescens extract on the viability of (a) A375 melanoma, (b) Colo-800 melanoma, (c) HDF α <t>fibroblast,</t> and (d) Hek 293 cells after 24, 48, and 72 h of treatment. The viability was assessed using the alamarBlue assay and expressed as percentage relative to the control-treated cells (0 mg/mL). Error bars represent the SEM ( n ≥ 3) and ∗ indicates a significant difference from 0 mg/mL ( P < 0.05).
Normal Human Dermal Fibroblast Alpha Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+primary+dermal+fibroblast+cell+line+hdf+%CE%B1/Primary+Dermal+Fibroblast%3B+Normal%2C+Human%2C+Adult/pmc12965329-66-0-8
Average 99 stars, based on 1 article reviews
normal human dermal fibroblast alpha cells - by Bioz Stars, 2026-09
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hdf-α cell line  (ScienCell)
90
ScienCell hdf-α cell line
The effect of S. frutescens extract on the viability of (a) A375 melanoma, (b) Colo-800 melanoma, (c) HDF α <t>fibroblast,</t> and (d) Hek 293 cells after 24, 48, and 72 h of treatment. The viability was assessed using the alamarBlue assay and expressed as percentage relative to the control-treated cells (0 mg/mL). Error bars represent the SEM ( n ≥ 3) and ∗ indicates a significant difference from 0 mg/mL ( P < 0.05).
Hdf α Cell Line, supplied by ScienCell, 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/human+primary+dermal+fibroblast+cell+line+hdf+%CE%B1/hdf+a+cells/pmc07868849-130-1-8
Average 90 stars, based on 1 article reviews
hdf-α cell line - by Bioz Stars, 2026-09
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dermal fibroblasts hdf α  (Cell Applications Inc)
96
Cell Applications Inc dermal fibroblasts hdf α
The effect of S. frutescens extract on the viability of (a) A375 melanoma, (b) Colo-800 melanoma, (c) HDF α <t>fibroblast,</t> and (d) Hek 293 cells after 24, 48, and 72 h of treatment. The viability was assessed using the alamarBlue assay and expressed as percentage relative to the control-treated cells (0 mg/mL). Error bars represent the SEM ( n ≥ 3) and ∗ indicates a significant difference from 0 mg/mL ( P < 0.05).
Dermal Fibroblasts Hdf α, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+primary+dermal+fibroblast+cell+line+hdf+%CE%B1/Human+Dermal+Fibroblasts%3A+HDF/pm25997157-289-7-10
Average 96 stars, based on 1 article reviews
dermal fibroblasts hdf α - by Bioz Stars, 2026-09
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high glucose induction human dermal fibroblasts hdfs  (Thermo Fisher)
99
Thermo Fisher high glucose induction human dermal fibroblasts hdfs
The effect of S. frutescens extract on the viability of (a) A375 melanoma, (b) Colo-800 melanoma, (c) HDF α <t>fibroblast,</t> and (d) Hek 293 cells after 24, 48, and 72 h of treatment. The viability was assessed using the alamarBlue assay and expressed as percentage relative to the control-treated cells (0 mg/mL). Error bars represent the SEM ( n ≥ 3) and ∗ indicates a significant difference from 0 mg/mL ( P < 0.05).
High Glucose Induction Human Dermal Fibroblasts Hdfs, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+primary+dermal+fibroblast+cell+line+hdf+%CE%B1/D(%2B)-Glucose/10__1620_slash_tjem__2023__j078-43-3-18
Average 99 stars, based on 1 article reviews
high glucose induction human dermal fibroblasts hdfs - by Bioz Stars, 2026-09
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antibodies anti lamin a c  (Santa Cruz Biotechnology)
96
Santa Cruz Biotechnology antibodies anti lamin a c
( A ) Representative immunolabeling for lamin <t>A/C</t> (red) and Prelamin A (red) of WT and <t>DCM</t> <t>HDFs</t> (IV-7, IV-9, and III-2). Nuclei are counterstained with Hoechst 33,342 (blue). Scale bar 20 µm, 100 µm. ( B ) Percentage of WT and DCM cells with abnormal nuclear irregularities revealed in HDFs patients. Results represent three independent experiments with significant differences between WT and DCM HDFs (** p < 0.01). ( C ) Bar graphs represent the four parameters relative to nuclear shape (area; circularity; elongation; roundness); they are reported as mean values ± SD (fold DCM vs. WT) of three independent experiments. Significant differences are denoted by the p -value (Student’s two-tailed t -test; * p < 0.05. ( D ) RT-qPCR of lamin A and C transcripts in WT and DCM HDFs; GAPDH was used as reference gene. Data are from three independent experiments and represented as mean ± SD (* p < 0.05). ( E ) Densitometric analysis of Western blot performed on WT and DCM HDFs, showing the intensity of the band corresponding to lamin A and C normalized versus β-actin levels. WT densitometric value is the average between two different controls (* p < 0.05; ** p < 0.01). Data are presented as mean ± SD. ( F ) Representative Western blot of lamin A and C; β-actin is used as housekeeping gene.
Antibodies Anti Lamin A C, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+primary+dermal+fibroblast+cell+line+hdf+%CE%B1/Lamin+A%2FC+Antibody/pmc08584896-92-5-10
Average 96 stars, based on 1 article reviews
antibodies anti lamin a c - by Bioz Stars, 2026-09
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endothelial growth medium egm 2  (Cell Applications Inc)
96
Cell Applications Inc endothelial growth medium egm 2
( A ) Representative immunolabeling for lamin <t>A/C</t> (red) and Prelamin A (red) of WT and <t>DCM</t> <t>HDFs</t> (IV-7, IV-9, and III-2). Nuclei are counterstained with Hoechst 33,342 (blue). Scale bar 20 µm, 100 µm. ( B ) Percentage of WT and DCM cells with abnormal nuclear irregularities revealed in HDFs patients. Results represent three independent experiments with significant differences between WT and DCM HDFs (** p < 0.01). ( C ) Bar graphs represent the four parameters relative to nuclear shape (area; circularity; elongation; roundness); they are reported as mean values ± SD (fold DCM vs. WT) of three independent experiments. Significant differences are denoted by the p -value (Student’s two-tailed t -test; * p < 0.05. ( D ) RT-qPCR of lamin A and C transcripts in WT and DCM HDFs; GAPDH was used as reference gene. Data are from three independent experiments and represented as mean ± SD (* p < 0.05). ( E ) Densitometric analysis of Western blot performed on WT and DCM HDFs, showing the intensity of the band corresponding to lamin A and C normalized versus β-actin levels. WT densitometric value is the average between two different controls (* p < 0.05; ** p < 0.01). Data are presented as mean ± SD. ( F ) Representative Western blot of lamin A and C; β-actin is used as housekeeping gene.
Endothelial Growth Medium Egm 2, supplied by Cell Applications Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/human+primary+dermal+fibroblast+cell+line+hdf+%CE%B1/Major+Media/pmc07085248-40-28-39
Average 96 stars, based on 1 article reviews
endothelial growth medium egm 2 - by Bioz Stars, 2026-09
96/100 stars
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ythdf1 antibody - n-terminal region (oasg02075)  (Aviva Systems)
N/A
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anti-ythdf2 (aa 316-564) polyclonal antibody  (Creative BioMart)
N/A
YTHDF2 (YTH domain family, member 2) is a protein-coding gene. Diseases associated with YTHDF2 include acute myeloid leukemia, and myeloid leukemia. An important paralog of this gene is YTHDF1.Shipped at 4°C. Store at 4°C short
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rcombinant anti-human ythdf2 antibody  (Creative BioMart)
N/A
Recombinant Mouse Antibody binds selectively to Human YTHDF2, expressed in Chinese Hamster Ovary cells(CHO).Used for immunoassaytechniques such as: Enzyme-linked Immunosorbent Assay; Western blot; Immunofluorescence; Functional Study4°C. For long term storage, aliquot and store at -20°C.
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ythdf2 antibody  (Cell Signaling Technology Inc)
N/A
N6-methyladenosine (m6A) is an abundant RNA modification that plays an important role in mRNA splicing, processing, and stability. The m6A modification is specifically recognized by members of the YT521B homology (YTH) domain-containing family (YTHDF), consisting
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anti-ythdf1 antibody  (St Johns Laboratory)
N/A
Conjugation note: Unconjugated Application note: WB Reactivity note: Human,Mouse
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Image Search Results


The effect of S. frutescens extract on the viability of (a) A375 melanoma, (b) Colo-800 melanoma, (c) HDF α fibroblast, and (d) Hek 293 cells after 24, 48, and 72 h of treatment. The viability was assessed using the alamarBlue assay and expressed as percentage relative to the control-treated cells (0 mg/mL). Error bars represent the SEM ( n ≥ 3) and ∗ indicates a significant difference from 0 mg/mL ( P < 0.05).

Journal: Evidence-based Complementary and Alternative Medicine : eCAM

Article Title: The Induction of Apoptosis in A375 Malignant Melanoma Cells by Sutherlandia frutescens

doi: 10.1155/2016/4921067

Figure Lengend Snippet: The effect of S. frutescens extract on the viability of (a) A375 melanoma, (b) Colo-800 melanoma, (c) HDF α fibroblast, and (d) Hek 293 cells after 24, 48, and 72 h of treatment. The viability was assessed using the alamarBlue assay and expressed as percentage relative to the control-treated cells (0 mg/mL). Error bars represent the SEM ( n ≥ 3) and ∗ indicates a significant difference from 0 mg/mL ( P < 0.05).

Article Snippet: The human primary dermal fibroblast cell line (HDF α ) was purchased from ScienCell, CA, USA.

Techniques: Alamar Blue Assay, Control

( A ) Representative immunolabeling for lamin A/C (red) and Prelamin A (red) of WT and DCM HDFs (IV-7, IV-9, and III-2). Nuclei are counterstained with Hoechst 33,342 (blue). Scale bar 20 µm, 100 µm. ( B ) Percentage of WT and DCM cells with abnormal nuclear irregularities revealed in HDFs patients. Results represent three independent experiments with significant differences between WT and DCM HDFs (** p < 0.01). ( C ) Bar graphs represent the four parameters relative to nuclear shape (area; circularity; elongation; roundness); they are reported as mean values ± SD (fold DCM vs. WT) of three independent experiments. Significant differences are denoted by the p -value (Student’s two-tailed t -test; * p < 0.05. ( D ) RT-qPCR of lamin A and C transcripts in WT and DCM HDFs; GAPDH was used as reference gene. Data are from three independent experiments and represented as mean ± SD (* p < 0.05). ( E ) Densitometric analysis of Western blot performed on WT and DCM HDFs, showing the intensity of the band corresponding to lamin A and C normalized versus β-actin levels. WT densitometric value is the average between two different controls (* p < 0.05; ** p < 0.01). Data are presented as mean ± SD. ( F ) Representative Western blot of lamin A and C; β-actin is used as housekeeping gene.

Journal: Journal of Clinical Medicine

Article Title: Clinical Features of LMNA-Related Cardiomyopathy in 18 Patients and Characterization of Two Novel Variants

doi: 10.3390/jcm10215075

Figure Lengend Snippet: ( A ) Representative immunolabeling for lamin A/C (red) and Prelamin A (red) of WT and DCM HDFs (IV-7, IV-9, and III-2). Nuclei are counterstained with Hoechst 33,342 (blue). Scale bar 20 µm, 100 µm. ( B ) Percentage of WT and DCM cells with abnormal nuclear irregularities revealed in HDFs patients. Results represent three independent experiments with significant differences between WT and DCM HDFs (** p < 0.01). ( C ) Bar graphs represent the four parameters relative to nuclear shape (area; circularity; elongation; roundness); they are reported as mean values ± SD (fold DCM vs. WT) of three independent experiments. Significant differences are denoted by the p -value (Student’s two-tailed t -test; * p < 0.05. ( D ) RT-qPCR of lamin A and C transcripts in WT and DCM HDFs; GAPDH was used as reference gene. Data are from three independent experiments and represented as mean ± SD (* p < 0.05). ( E ) Densitometric analysis of Western blot performed on WT and DCM HDFs, showing the intensity of the band corresponding to lamin A and C normalized versus β-actin levels. WT densitometric value is the average between two different controls (* p < 0.05; ** p < 0.01). Data are presented as mean ± SD. ( F ) Representative Western blot of lamin A and C; β-actin is used as housekeeping gene.

Article Snippet: HDFs were incubated with primary antibodies anti-Lamin A/C (N-18, sc-6215, Santa Cruz Biotechnology) and anti-prelamin A (C-20, sc-6214, Santa Cruz Biotechnology), as described [ ].

Techniques: Immunolabeling, Two Tailed Test, Quantitative RT-PCR, Western Blot