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gene exp abcg2 hs01053790 m1  (Thermo Fisher)


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    Thermo Fisher gene exp abcg2 hs01053790 m1
    Gene Exp Abcg2 Hs01053790 M1, 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/abcg2/Gene+Exp%2E+ABCG2%2C+Hs01053790_m1/pm41998207-59-1-23
    Average 99 stars, based on 1 article reviews
    gene exp abcg2 hs01053790 m1 - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Transfection:

    Article Title: The multidrug resistance transporter P-glycoprotein confers resistance to ferroptosis inducers
    Article Snippet: .. A673 cells (from ATCC, Manassas, VA) were seeded and transfected with empty vector (EV) or vector containing full-length, human ABCB1 or ABCG2 using Lipofectamine 2000 (Invitrogen, Waltham, MA). ..

    Plasmid Preparation:

    Article Title: The multidrug resistance transporter P-glycoprotein confers resistance to ferroptosis inducers
    Article Snippet: .. A673 cells (from ATCC, Manassas, VA) were seeded and transfected with empty vector (EV) or vector containing full-length, human ABCB1 or ABCG2 using Lipofectamine 2000 (Invitrogen, Waltham, MA). ..

    other:

    Article Title: Effect of Walker A mutation (K86M) on oligomerization and surface targeting of the multidrug resistance transporter ABCG2.
    Article Snippet: Antibodies against the following were used: ABCG2, ABCG2-PE and IgG-PE (eBioscience, San Diego, CA), BXP-21 (Alexis Biochemicals, Montreal, Canada), mHA.11, calnexin and giantin (Nordic Biosite AB, Täby, Sweden), MYC (Roche, Basel, Switzerland), β-actin (Sigma, St Louis, MO), rab5 and mouse IL-2Rα (Santa Cruz Biotechnologies, Santa Cruz, CA).

    Real-time Polymerase Chain Reaction:

    Article Title: Distinct epigenetic profiling in head and neck squamous cell carcinoma stem cells.
    Article Snippet: Objective.. To identify unique epigenetic signature in cancer stem cells (CSCs) in head and neck squamous cell carcinoma (HNSCC).. Study Design.

    Article Title: Kr?ppel-Like Factor 5 Is Not Required for K-Ras G12D Lung Tumorigenesis, but Represses ABCG2 Expression and Is Associated with Better Disease-Specific Survival
    Article Snippet: Verapamil-sensitive SP were quantified using FloJo software (Treestar, Ashland, OR). .. RNA Isolation and Real-Time PCR Total RNA was isolated with the RNeasy Mini Kit (QIAGEN, Valencia, CA), digested with DNase1 (Applied Biosystems/Ambion, Austin, TX) to remove DNA contamination, and processed using the Taqman Reverse Transcription System according to the manufacturer’s instructions (Applied Biosystems, Foster City, CA). cDNA was analyzed with probes targeting KLF5 , ABCG2 , and β- actin (Applied Biosystems, Foster City, CA). ..

    Polymerase Chain Reaction:

    Article Title: Distinct epigenetic profiling in head and neck squamous cell carcinoma stem cells.
    Article Snippet: Objective.. To identify unique epigenetic signature in cancer stem cells (CSCs) in head and neck squamous cell carcinoma (HNSCC).. Study Design.

    Gene Expression:

    Article Title: Distinct epigenetic profiling in head and neck squamous cell carcinoma stem cells.
    Article Snippet: Objective.. To identify unique epigenetic signature in cancer stem cells (CSCs) in head and neck squamous cell carcinoma (HNSCC).. Study Design.

    Reverse Transcription:

    Article Title: Distinct epigenetic profiling in head and neck squamous cell carcinoma stem cells.
    Article Snippet: Objective.. To identify unique epigenetic signature in cancer stem cells (CSCs) in head and neck squamous cell carcinoma (HNSCC).. Study Design.

    Article Title: Kr?ppel-Like Factor 5 Is Not Required for K-Ras G12D Lung Tumorigenesis, but Represses ABCG2 Expression and Is Associated with Better Disease-Specific Survival
    Article Snippet: Verapamil-sensitive SP were quantified using FloJo software (Treestar, Ashland, OR). .. RNA Isolation and Real-Time PCR Total RNA was isolated with the RNeasy Mini Kit (QIAGEN, Valencia, CA), digested with DNase1 (Applied Biosystems/Ambion, Austin, TX) to remove DNA contamination, and processed using the Taqman Reverse Transcription System according to the manufacturer’s instructions (Applied Biosystems, Foster City, CA). cDNA was analyzed with probes targeting KLF5 , ABCG2 , and β- actin (Applied Biosystems, Foster City, CA). ..

    Isolation:

    Article Title: Kr?ppel-Like Factor 5 Is Not Required for K-Ras G12D Lung Tumorigenesis, but Represses ABCG2 Expression and Is Associated with Better Disease-Specific Survival
    Article Snippet: Verapamil-sensitive SP were quantified using FloJo software (Treestar, Ashland, OR). .. RNA Isolation and Real-Time PCR Total RNA was isolated with the RNeasy Mini Kit (QIAGEN, Valencia, CA), digested with DNase1 (Applied Biosystems/Ambion, Austin, TX) to remove DNA contamination, and processed using the Taqman Reverse Transcription System according to the manufacturer’s instructions (Applied Biosystems, Foster City, CA). cDNA was analyzed with probes targeting KLF5 , ABCG2 , and β- actin (Applied Biosystems, Foster City, CA). ..



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    Effects of L-carnitine on intestinal morphology, barrier-related proteins, and urate transporter expression in hyperuricemic mice. (A) H&E staining of intestinal tissue sections. (B) Immunofluorescence staining of Occludin and ZO-1 in the small intestine ( n = 3 per group). (C) Representative protein expression of intestinal urate transport-related proteins. (D) Quantitative analysis of intestinal urate transport-related protein expression ( n = 3 per group). (E) Immunofluorescence staining of <t>ABCG2</t> in the small intestine ( n = 3 per group). Data are presented as mean ± SEM. ns, not significant; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. CG; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. HUG.
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    Effects of L-carnitine on intestinal morphology, barrier-related proteins, and urate transporter expression in hyperuricemic mice. (A) H&E staining of intestinal tissue sections. (B) Immunofluorescence staining of Occludin and ZO-1 in the small intestine ( n = 3 per group). (C) Representative protein expression of intestinal urate transport-related proteins. (D) Quantitative analysis of intestinal urate transport-related protein expression ( n = 3 per group). (E) Immunofluorescence staining of <t>ABCG2</t> in the small intestine ( n = 3 per group). Data are presented as mean ± SEM. ns, not significant; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. CG; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. HUG.
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    Expected outcome of the PLA analysis of an overexpressed viral protein and an endogenous protein (A) Representative images of PLA protocol performed in cells either transfected with a vector control or a vector encoding for StrepII-tagged SARS-CoV-2 E T9 (wildtype) or the T9I variant. Cells are incubated with the individual antibodies targeted against StrepII-tag or the endogenous target <t>ABCG2.</t> Red, PLA; blue, DAPI. Scale bar: 20 μm (B) Quantification of the immunofluorescence images of (A). Lines represent the mean of N = 19-70 (individual cells) ± SEM.
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    Image Search Results


    Effects of L-carnitine on intestinal morphology, barrier-related proteins, and urate transporter expression in hyperuricemic mice. (A) H&E staining of intestinal tissue sections. (B) Immunofluorescence staining of Occludin and ZO-1 in the small intestine ( n = 3 per group). (C) Representative protein expression of intestinal urate transport-related proteins. (D) Quantitative analysis of intestinal urate transport-related protein expression ( n = 3 per group). (E) Immunofluorescence staining of ABCG2 in the small intestine ( n = 3 per group). Data are presented as mean ± SEM. ns, not significant; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. CG; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. HUG.

    Journal: Frontiers in Nutrition

    Article Title: Oral L-carnitine supplementation lowers serum uric acid and is associated with renal and intestinal urate-handling responses in hyperuricemic mice

    doi: 10.3389/fnut.2026.1866695

    Figure Lengend Snippet: Effects of L-carnitine on intestinal morphology, barrier-related proteins, and urate transporter expression in hyperuricemic mice. (A) H&E staining of intestinal tissue sections. (B) Immunofluorescence staining of Occludin and ZO-1 in the small intestine ( n = 3 per group). (C) Representative protein expression of intestinal urate transport-related proteins. (D) Quantitative analysis of intestinal urate transport-related protein expression ( n = 3 per group). (E) Immunofluorescence staining of ABCG2 in the small intestine ( n = 3 per group). Data are presented as mean ± SEM. ns, not significant; # p < 0.05, ## p < 0.01, ### p < 0.001 vs. CG; * p < 0.05, ** p < 0.01, *** p < 0.001 vs. HUG.

    Article Snippet: After blocking with 5% non-fat milk in Tris-buffered saline containing 0.1% Tween 20 (TBST) for 1 h at room temperature, the membranes were incubated overnight at 4 °C with the following primary antibodies: XOD (1:2000, Cat. No. 55156-1-AP, Proteintech), ADA (1:2000, Cat. No. 67870-1-Ig, Proteintech), OAT1 (1:2000, Cat. No. 26574-1-AP, Proteintech), OAT3 (1:2000, Cat. No. bs-0609R, Bioss), GLUT9 (1:1000, Cat. No. 26486-1-AP, Proteintech), ABCG2 (1:1000, Cat. No. 27286-1-AP, Proteintech), URAT1 (1:3000, Cat. No. 14937-1-AP, Proteintech), IκBα (1:1000, Cat. No. GB111509 , Servicebio), NF-κB p65 (1:2000, Cat. No. 66535-1-Ig, Proteintech), phospho-NF-κB p65 (1:2000, Cat. No. ZHS1565, ZhongHe) and β-actin (1:8000, Cat. No. 66009-1-Ig, Proteintech).

    Techniques: Morphology, Expressing, Staining, Tissue, Immunofluorescence, Analysis

    Expected outcome of the PLA analysis of an overexpressed viral protein and an endogenous protein (A) Representative images of PLA protocol performed in cells either transfected with a vector control or a vector encoding for StrepII-tagged SARS-CoV-2 E T9 (wildtype) or the T9I variant. Cells are incubated with the individual antibodies targeted against StrepII-tag or the endogenous target ABCG2. Red, PLA; blue, DAPI. Scale bar: 20 μm (B) Quantification of the immunofluorescence images of (A). Lines represent the mean of N = 19-70 (individual cells) ± SEM.

    Journal: STAR Protocols

    Article Title: Protocol to differentially quantify spatially resolved viral protein-cellular protein interactions via proximity ligation assays

    doi: 10.1016/j.xpro.2026.104361

    Figure Lengend Snippet: Expected outcome of the PLA analysis of an overexpressed viral protein and an endogenous protein (A) Representative images of PLA protocol performed in cells either transfected with a vector control or a vector encoding for StrepII-tagged SARS-CoV-2 E T9 (wildtype) or the T9I variant. Cells are incubated with the individual antibodies targeted against StrepII-tag or the endogenous target ABCG2. Red, PLA; blue, DAPI. Scale bar: 20 μm (B) Quantification of the immunofluorescence images of (A). Lines represent the mean of N = 19-70 (individual cells) ± SEM.

    Article Snippet: Monoclonal mouse anti-ABCG2 Antibody (BXP-21) (PLA 1:100) , Santa Cruz Biotechnology , Cat#sc-58222; RRID: AB_630828.

    Techniques: Transfection, Plasmid Preparation, Control, Variant Assay, Incubation, Immunofluorescence