human skin fibroblasts bj 5ta cell line Search Results


98
ATCC human skin fibroblasts
Human Skin Fibroblasts, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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LGC Standards alpha-hydroxymidazolam (1.0 mg/ml) in methanol
Alpha Hydroxymidazolam (1.0 Mg/Ml) In Methanol, supplied by LGC Standards, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC bj 5ta htert immortalized human fibroblasts
(A) WB of CSB, HTRA3 (left panel), and CTSB, and p21 (right panel) in BJ fibroblasts untreated and 10 days post-irradiation using ß-tubulin and GAPDH, respectively, as loading control. (B) Scheme showing the two hypotheses for the mechanism leading to senescence-related HTRA3 and CTSB overexpression. (C) Immunoblots of p21, CSB, HTRA3, CTSB, and POLG1 in <t>BJ-5ta</t> hTERT WT fibroblasts and 2 CRISPR-edited CSB knocked-out clones (BJ-5ta csb-/- hTERT #1 and BJ-5ta csb-/- hTERT #2). Frames show samples on the same blot; each displaying the respective GAPDH used as loading control. (D) Scheme indicating normally blocked senescence in BJ-5ta hTERT cells and activation of senescence upon irradiation at 10 Gy. WB analysis of (E) CSB, CTSB, p21, and (F) HTRA3 three days post-irradiation in BJ-5ta hTERT WT fibroblasts and BJ-5ta hTERT CSB knocked-out fibroblasts (β-tubulin was used as loading control). RT-qPCR of ( G ) p21 Waf1 and ( H ) HTRA3 and ( I ) CTSB in the same experiment and cells schematized in panel D. Samples on the same blot are framed; each frame displays the respective GAPDH or β-tubulin used as loading control. RT-qPCR: n=3 independent experiments; mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001; based on unpaired t test comparisons to respective non-irradiated control.
Bj 5ta Htert Immortalized Human Fibroblasts, 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
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93
ATCC human foreskin fibroblast bj 5ta
(A) WB of CSB, HTRA3 (left panel), and CTSB, and p21 (right panel) in BJ fibroblasts untreated and 10 days post-irradiation using ß-tubulin and GAPDH, respectively, as loading control. (B) Scheme showing the two hypotheses for the mechanism leading to senescence-related HTRA3 and CTSB overexpression. (C) Immunoblots of p21, CSB, HTRA3, CTSB, and POLG1 in <t>BJ-5ta</t> hTERT WT fibroblasts and 2 CRISPR-edited CSB knocked-out clones (BJ-5ta csb-/- hTERT #1 and BJ-5ta csb-/- hTERT #2). Frames show samples on the same blot; each displaying the respective GAPDH used as loading control. (D) Scheme indicating normally blocked senescence in BJ-5ta hTERT cells and activation of senescence upon irradiation at 10 Gy. WB analysis of (E) CSB, CTSB, p21, and (F) HTRA3 three days post-irradiation in BJ-5ta hTERT WT fibroblasts and BJ-5ta hTERT CSB knocked-out fibroblasts (β-tubulin was used as loading control). RT-qPCR of ( G ) p21 Waf1 and ( H ) HTRA3 and ( I ) CTSB in the same experiment and cells schematized in panel D. Samples on the same blot are framed; each frame displays the respective GAPDH or β-tubulin used as loading control. RT-qPCR: n=3 independent experiments; mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001; based on unpaired t test comparisons to respective non-irradiated control.
Human Foreskin Fibroblast Bj 5ta, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC bj t atcc cat
(A) WB of CSB, HTRA3 (left panel), and CTSB, and p21 (right panel) in BJ fibroblasts untreated and 10 days post-irradiation using ß-tubulin and GAPDH, respectively, as loading control. (B) Scheme showing the two hypotheses for the mechanism leading to senescence-related HTRA3 and CTSB overexpression. (C) Immunoblots of p21, CSB, HTRA3, CTSB, and POLG1 in <t>BJ-5ta</t> hTERT WT fibroblasts and 2 CRISPR-edited CSB knocked-out clones (BJ-5ta csb-/- hTERT #1 and BJ-5ta csb-/- hTERT #2). Frames show samples on the same blot; each displaying the respective GAPDH used as loading control. (D) Scheme indicating normally blocked senescence in BJ-5ta hTERT cells and activation of senescence upon irradiation at 10 Gy. WB analysis of (E) CSB, CTSB, p21, and (F) HTRA3 three days post-irradiation in BJ-5ta hTERT WT fibroblasts and BJ-5ta hTERT CSB knocked-out fibroblasts (β-tubulin was used as loading control). RT-qPCR of ( G ) p21 Waf1 and ( H ) HTRA3 and ( I ) CTSB in the same experiment and cells schematized in panel D. Samples on the same blot are framed; each frame displays the respective GAPDH or β-tubulin used as loading control. RT-qPCR: n=3 independent experiments; mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001; based on unpaired t test comparisons to respective non-irradiated control.
Bj T Atcc Cat, 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
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98
ATCC human foreskin fibroblast cells
(A) WB of CSB, HTRA3 (left panel), and CTSB, and p21 (right panel) in BJ fibroblasts untreated and 10 days post-irradiation using ß-tubulin and GAPDH, respectively, as loading control. (B) Scheme showing the two hypotheses for the mechanism leading to senescence-related HTRA3 and CTSB overexpression. (C) Immunoblots of p21, CSB, HTRA3, CTSB, and POLG1 in <t>BJ-5ta</t> hTERT WT fibroblasts and 2 CRISPR-edited CSB knocked-out clones (BJ-5ta csb-/- hTERT #1 and BJ-5ta csb-/- hTERT #2). Frames show samples on the same blot; each displaying the respective GAPDH used as loading control. (D) Scheme indicating normally blocked senescence in BJ-5ta hTERT cells and activation of senescence upon irradiation at 10 Gy. WB analysis of (E) CSB, CTSB, p21, and (F) HTRA3 three days post-irradiation in BJ-5ta hTERT WT fibroblasts and BJ-5ta hTERT CSB knocked-out fibroblasts (β-tubulin was used as loading control). RT-qPCR of ( G ) p21 Waf1 and ( H ) HTRA3 and ( I ) CTSB in the same experiment and cells schematized in panel D. Samples on the same blot are framed; each frame displays the respective GAPDH or β-tubulin used as loading control. RT-qPCR: n=3 independent experiments; mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001; based on unpaired t test comparisons to respective non-irradiated control.
Human Foreskin Fibroblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
LGC Standards htert bj 5ta
GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell <t>line</t> <t>BJ-5ta.</t> Human fibroblast immortalized with <t>hTERT</t> (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.
Htert Bj 5ta, supplied by LGC Standards, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
LGC Standards bp-145
GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell <t>line</t> <t>BJ-5ta.</t> Human fibroblast immortalized with <t>hTERT</t> (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.
Bp 145, supplied by LGC Standards, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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97
LGC Standards crl-4001
GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell <t>line</t> <t>BJ-5ta.</t> Human fibroblast immortalized with <t>hTERT</t> (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.
Crl 4001, supplied by LGC Standards, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
LGC Standards cupri-tartaric solution 1
GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell <t>line</t> <t>BJ-5ta.</t> Human fibroblast immortalized with <t>hTERT</t> (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.
Cupri Tartaric Solution 1, supplied by LGC Standards, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC escherichia coli (migula) castellani and chalmers
GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell <t>line</t> <t>BJ-5ta.</t> Human fibroblast immortalized with <t>hTERT</t> (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.
Escherichia Coli (Migula) Castellani And Chalmers, 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
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95
ATCC intestine 407
GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell <t>line</t> <t>BJ-5ta.</t> Human fibroblast immortalized with <t>hTERT</t> (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.
Intestine 407, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


(A) WB of CSB, HTRA3 (left panel), and CTSB, and p21 (right panel) in BJ fibroblasts untreated and 10 days post-irradiation using ß-tubulin and GAPDH, respectively, as loading control. (B) Scheme showing the two hypotheses for the mechanism leading to senescence-related HTRA3 and CTSB overexpression. (C) Immunoblots of p21, CSB, HTRA3, CTSB, and POLG1 in BJ-5ta hTERT WT fibroblasts and 2 CRISPR-edited CSB knocked-out clones (BJ-5ta csb-/- hTERT #1 and BJ-5ta csb-/- hTERT #2). Frames show samples on the same blot; each displaying the respective GAPDH used as loading control. (D) Scheme indicating normally blocked senescence in BJ-5ta hTERT cells and activation of senescence upon irradiation at 10 Gy. WB analysis of (E) CSB, CTSB, p21, and (F) HTRA3 three days post-irradiation in BJ-5ta hTERT WT fibroblasts and BJ-5ta hTERT CSB knocked-out fibroblasts (β-tubulin was used as loading control). RT-qPCR of ( G ) p21 Waf1 and ( H ) HTRA3 and ( I ) CTSB in the same experiment and cells schematized in panel D. Samples on the same blot are framed; each frame displays the respective GAPDH or β-tubulin used as loading control. RT-qPCR: n=3 independent experiments; mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001; based on unpaired t test comparisons to respective non-irradiated control.

Journal: bioRxiv

Article Title: HTRA3 protease-chaperone stabilizes cathepsin B for mitochondrial POLG1 depletion in human cell ageing

doi: 10.1101/2025.07.21.647696

Figure Lengend Snippet: (A) WB of CSB, HTRA3 (left panel), and CTSB, and p21 (right panel) in BJ fibroblasts untreated and 10 days post-irradiation using ß-tubulin and GAPDH, respectively, as loading control. (B) Scheme showing the two hypotheses for the mechanism leading to senescence-related HTRA3 and CTSB overexpression. (C) Immunoblots of p21, CSB, HTRA3, CTSB, and POLG1 in BJ-5ta hTERT WT fibroblasts and 2 CRISPR-edited CSB knocked-out clones (BJ-5ta csb-/- hTERT #1 and BJ-5ta csb-/- hTERT #2). Frames show samples on the same blot; each displaying the respective GAPDH used as loading control. (D) Scheme indicating normally blocked senescence in BJ-5ta hTERT cells and activation of senescence upon irradiation at 10 Gy. WB analysis of (E) CSB, CTSB, p21, and (F) HTRA3 three days post-irradiation in BJ-5ta hTERT WT fibroblasts and BJ-5ta hTERT CSB knocked-out fibroblasts (β-tubulin was used as loading control). RT-qPCR of ( G ) p21 Waf1 and ( H ) HTRA3 and ( I ) CTSB in the same experiment and cells schematized in panel D. Samples on the same blot are framed; each frame displays the respective GAPDH or β-tubulin used as loading control. RT-qPCR: n=3 independent experiments; mean ± SD. * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001; based on unpaired t test comparisons to respective non-irradiated control.

Article Snippet: Normal female human foetal lung IMR-90 fibroblasts (ATCC; CCL-186) and BJ skin fibroblasts (ATCC; CRL-2522) were cultured in minimum essential medium (MEM, Gibco) supplemented with 2 mM L-glutamin (GlutMAX), 10% FBS, 1% Penicillin–streptomycin, 1% nonessential amino acids (Gibco) and 1% sodium pyruvate (Gibco) BJ-5ta hTERT immortalized human fibroblasts (ATCC; CCL-186) cultured in a 4:1 mixture of DMEM and Medium 199 (Gibco) supplemented with 10% FBS and1% Penicillin–streptomycin.

Techniques: Irradiation, Control, Over Expression, Western Blot, CRISPR, Clone Assay, Activation Assay, Quantitative RT-PCR

GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell line BJ-5ta. Human fibroblast immortalized with hTERT (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.

Journal: International Journal of Molecular Sciences

Article Title: GLUT10—Lacking in Arterial Tortuosity Syndrome—Is Localized to the Endoplasmic Reticulum of Human Fibroblasts

doi: 10.3390/ijms18081820

Figure Lengend Snippet: GLUT10 immunostaining and mitochondrial decoration with a fluorescent probe in the human fibroblast cell line BJ-5ta. Human fibroblast immortalized with hTERT (BJ-5ta line) were immunoreacted with the anti-GLUT10 antibody Ab2, and the mitochondrial fluorescent probe Mito Tracker™ Orange as reported in the “Experimental” section. Images were acquired by fluorescent microscopy as detailed in the “Experimental” section. Scale bar = 5 μm.

Article Snippet: A human skin fibroblast cell line immortalized with hTERT (BJ-5ta) was purchased from LGC Standards (Teddington, Middlesex, UK).

Techniques: Immunostaining, Microscopy