Human Hepatic Stellate Cells Search Results


96
Cell Applications Inc hskmc growth medium
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iXCells Biotechnologies cell cultures human hepatic stellate cells
Cell Cultures Human Hepatic Stellate Cells, supplied by iXCells Biotechnologies, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Elabscience Biotechnology human hepatic stellate cell line lx 2
Human Hepatic Stellate Cell Line Lx 2, supplied by Elabscience Biotechnology, 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+Hepatic+Stellate+Cells/pm33542321-281-0-21?v=Elabscience+Biotechnology
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Innoprot Inc primary hepatic stellate cells hhsc
Primary Hepatic Stellate Cells Hhsc, supplied by Innoprot Inc, 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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Axol Bioscience human intrahepatic biliary epithelial cells
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Human Intrahepatic Biliary Epithelial Cells, supplied by Axol Bioscience, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/Human+Hepatic+Stellate+Cells/pmc07805240-66-3-8?v=Axol+Bioscience
Average 91 stars, based on 1 article reviews
human intrahepatic biliary epithelial cells - by Bioz Stars, 2026-07
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90
Celprogen Inc extracellular matrix
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Extracellular Matrix, supplied by Celprogen Inc, 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+Hepatic+Stellate+Cells/pm29669510-73-20-28?v=Celprogen+Inc
Average 90 stars, based on 1 article reviews
extracellular matrix - by Bioz Stars, 2026-07
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BioIVT Inc primary human hepatic stellate cells (hhstec
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Primary Human Hepatic Stellate Cells (Hhstec, supplied by BioIVT Inc, 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+Hepatic+Stellate+Cells/bio_rxiv__2023__07__03__547412-159-0-7?v=BioIVT+Inc
Average 90 stars, based on 1 article reviews
primary human hepatic stellate cells (hhstec - by Bioz Stars, 2026-07
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Merck KGaA human hepatic stellate cell line lx-2
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Human Hepatic Stellate Cell Line Lx 2, supplied by Merck KGaA, 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+Hepatic+Stellate+Cells/pmc08169952-347-18-24?v=Merck+KGaA
Average 90 stars, based on 1 article reviews
human hepatic stellate cell line lx-2 - by Bioz Stars, 2026-07
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ScienCell culture-activated human hepatic stellate cells (hscs) hhstec 5300
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Culture Activated Human Hepatic Stellate Cells (Hscs) Hhstec 5300, 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+Hepatic+Stellate+Cells/pm30055117-145-9-11?v=ScienCell
Average 90 stars, based on 1 article reviews
culture-activated human hepatic stellate cells (hscs) hhstec 5300 - by Bioz Stars, 2026-07
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3H Biomedical primary human hepatic stellate cells cryopreserved after purification from human liver
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Primary Human Hepatic Stellate Cells Cryopreserved After Purification From Human Liver, supplied by 3H Biomedical, 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+Hepatic+Stellate+Cells/pmc05886043-120-8-15?v=3H+Biomedical
Average 90 stars, based on 1 article reviews
primary human hepatic stellate cells cryopreserved after purification from human liver - by Bioz Stars, 2026-07
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Lonza primary human hepatic stellate cells (hscs)
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Primary Human Hepatic Stellate Cells (Hscs), supplied by Lonza, 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+Hepatic+Stellate+Cells/pm40025044-237-3-14?v=Lonza
Average 90 stars, based on 1 article reviews
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China Center for Type Culture Collection human hepatic stellate cell line lx-2
SHED-HepT reconstructs <t>intrahepatic</t> bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, <t>human</t> primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem <t>cells</t> in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: <t>epithelial</t> cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms
Human Hepatic Stellate Cell Line Lx 2, supplied by China Center for Type Culture Collection, 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+Hepatic+Stellate+Cells/pmc10787101-209-0-10?v=China+Center+for+Type+Culture+Collection
Average 90 stars, based on 1 article reviews
human hepatic stellate cell line lx-2 - by Bioz Stars, 2026-07
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Image Search Results


SHED-HepT reconstructs intrahepatic bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, human primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem cells in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: epithelial cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms

Journal: Stem Cell Research & Therapy

Article Title: Cholangiogenic potential of human deciduous pulp stem cell-converted hepatocyte-like cells

doi: 10.1186/s13287-020-02113-8

Figure Lengend Snippet: SHED-HepT reconstructs intrahepatic bile ducts in livers of recipient CCl 4 -treated mice. a–e In vitro hepatobiliary function was analyzed in SHED-Heps. Gene expression of uridine 5′-diphospho-glucuronosyltransferase 1A1 ( UGT1A1 ) by reverse transcription-quantitative polymerase chain reaction (RT-qPCR). Amount of direct bilirubin by colorimetric assay ( b ). Representative images of bile transport were detected by CLF staining. Nuclei were stained with DAPI ( c ). Gene expression of membrane metalloendopeptidase ( MME ), ATP-binding cassette transporter B1 ( ABCB1 ), ABCB11, and ABCC2 by RT-qPCR d . Representative images of the expression of MME, ABCB1, ABCB11, and ABCC2 were detected by immunohistochemical analysis ( e ). a–e hPHep, human primary hepatocyte. a, b, d n = 5 for all groups. *** P < 0.005. nd, no detection. The graph bars represent the means ± SEM. a, d Results are shown as a ratio to hPHeps (hPHep = 1). c, e Scale bars, 20 μm. f, g Representative histograms of the expression of cell surface markers for hepatocyte progenitors and mesenchymal stem cells in SHED-Heps ( f ) and whole liver cells isolated from recipient mice (WLC) ( g ) were detected by FCM assay. EPCAM: epithelial cell adhesion molecule; MME: membrane metalloendopeptidase; NCAM1: neural cell adhesion molecule; PROM1: promin 1; R-PE: R-phycoerythrin. f Red solid line, target antibody-stained histograms; black solid line, isotype-matched control-stained histograms. g Area filed with red, target antibody-stained histograms; solid line, isotype-matched control-stained histograms

Article Snippet: Intact SHED and human intrahepatic biliary epithelial cells (AXOL, Cambridge, UK) were used as controls.

Techniques: In Vitro, Expressing, Real-time Polymerase Chain Reaction, Quantitative RT-PCR, Colorimetric Assay, Staining, Binding Assay, Immunohistochemical staining, Isolation