hrecs cat. Search Results


primary human renal tubular epithelial (hre) cells  (Lonza)
90
Lonza primary human renal tubular epithelial (hre) cells
Primary Human Renal Tubular Epithelial (Hre) Cells, 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/result/primary human renal tubular epithelial (hre) cells/product/Lonza
Average 90 stars, based on 1 article reviews
primary human renal tubular epithelial (hre) cells - by Bioz Stars, 2026-05
90/100 stars
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hrecs cat. #6530  (ScienCell)
90
ScienCell hrecs cat. #6530
Effects of Cx43 knockdown on HG-induced angiogenesis (A) Cx43 knockdown in <t>hRECs</t> was achieved through the transfection of the vector containing small hairpin RNA targeting Cx43 (sh-Cx43#1/2/3); Cx43 knockdown was confirmed using Immunoblotting. hRECs were subsequently transfected with sh-Cx43#2 (with better knocking down <t>efficiency),</t> <t>cultured</t> in normal or 60 mmol/L HG medium, and examined for tubule formation on Matrigel (B) ; ROS release using flow cytometry (C) ; the content of TNF-α, IL-1β, VEGFA, and ICAM-1 in culture medium using ELISA kits (D) . n = 3, *p < 0.05, **p < 0.01 compared with normal+sh-NC group; ## p < 0.01 compared with HG+sh-NC group.
Hrecs Cat. #6530, 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/result/hrecs cat. #6530/product/ScienCell
Average 90 stars, based on 1 article reviews
hrecs cat. #6530 - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier

Image Search Results


Effects of Cx43 knockdown on HG-induced angiogenesis (A) Cx43 knockdown in hRECs was achieved through the transfection of the vector containing small hairpin RNA targeting Cx43 (sh-Cx43#1/2/3); Cx43 knockdown was confirmed using Immunoblotting. hRECs were subsequently transfected with sh-Cx43#2 (with better knocking down efficiency), cultured in normal or 60 mmol/L HG medium, and examined for tubule formation on Matrigel (B) ; ROS release using flow cytometry (C) ; the content of TNF-α, IL-1β, VEGFA, and ICAM-1 in culture medium using ELISA kits (D) . n = 3, *p < 0.05, **p < 0.01 compared with normal+sh-NC group; ## p < 0.01 compared with HG+sh-NC group.

Journal: Frontiers in Endocrinology

Article Title: Connexin 43 (Cx43) regulates high-glucose-induced retinal endothelial cell angiogenesis and retinal neovascularization

doi: 10.3389/fendo.2022.909207

Figure Lengend Snippet: Effects of Cx43 knockdown on HG-induced angiogenesis (A) Cx43 knockdown in hRECs was achieved through the transfection of the vector containing small hairpin RNA targeting Cx43 (sh-Cx43#1/2/3); Cx43 knockdown was confirmed using Immunoblotting. hRECs were subsequently transfected with sh-Cx43#2 (with better knocking down efficiency), cultured in normal or 60 mmol/L HG medium, and examined for tubule formation on Matrigel (B) ; ROS release using flow cytometry (C) ; the content of TNF-α, IL-1β, VEGFA, and ICAM-1 in culture medium using ELISA kits (D) . n = 3, *p < 0.05, **p < 0.01 compared with normal+sh-NC group; ## p < 0.01 compared with HG+sh-NC group.

Article Snippet: hRECs (Cat. #6530, ScienCell, Carlsbad, CA, USA) were cultured (37°C, 5% CO 2 ) in Endothelial Cell Medium (ECM, Cat. #1001, ScienCell) containing 5% fetal bovine serum (FBS; Cat. #0025, ScienCell). hRECs were allocated into four groups: normal, low-HG (culture medium containing 20 mmol/L glucose), middle-HG (culture medium containing 60 mmol/L glucose), and high-HG (culture medium containing 120 mmol/L glucose).

Techniques: Knockdown, Transfection, Plasmid Preparation, Western Blot, Cell Culture, Flow Cytometry, Enzyme-linked Immunosorbent Assay

Effects of Cx43 overexpression on HG-induced angiogenesis (A) Cx43 overexpression in hRECs was achieved through transfection of the vector containing Cx43 gene coding sequence (Cx43 OE); Cx43 overexpression was confirmed using Immunoblotting. hRECs were subsequently transfected with Cx43 OE, cultured in normal or 60 mmol/L HG medium, and examined for tubule formation on Matrigel (B) ; ROS release using flow cytometry (C) ; the content of TNF-α, IL-1β, VEGFA, and ICAM-1 in culture medium using ELISA kits (D) . n = 3, **p < 0.01 compared with normal+vector group; ## p < 0.01 compared with HG+vector group.

Journal: Frontiers in Endocrinology

Article Title: Connexin 43 (Cx43) regulates high-glucose-induced retinal endothelial cell angiogenesis and retinal neovascularization

doi: 10.3389/fendo.2022.909207

Figure Lengend Snippet: Effects of Cx43 overexpression on HG-induced angiogenesis (A) Cx43 overexpression in hRECs was achieved through transfection of the vector containing Cx43 gene coding sequence (Cx43 OE); Cx43 overexpression was confirmed using Immunoblotting. hRECs were subsequently transfected with Cx43 OE, cultured in normal or 60 mmol/L HG medium, and examined for tubule formation on Matrigel (B) ; ROS release using flow cytometry (C) ; the content of TNF-α, IL-1β, VEGFA, and ICAM-1 in culture medium using ELISA kits (D) . n = 3, **p < 0.01 compared with normal+vector group; ## p < 0.01 compared with HG+vector group.

Article Snippet: hRECs (Cat. #6530, ScienCell, Carlsbad, CA, USA) were cultured (37°C, 5% CO 2 ) in Endothelial Cell Medium (ECM, Cat. #1001, ScienCell) containing 5% fetal bovine serum (FBS; Cat. #0025, ScienCell). hRECs were allocated into four groups: normal, low-HG (culture medium containing 20 mmol/L glucose), middle-HG (culture medium containing 60 mmol/L glucose), and high-HG (culture medium containing 120 mmol/L glucose).

Techniques: Over Expression, Transfection, Plasmid Preparation, Sequencing, Western Blot, Cell Culture, Flow Cytometry, Enzyme-linked Immunosorbent Assay