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Fisher Scientific infinity cholesterol liquid stable reagent kit
Infinity Cholesterol Liquid Stable Reagent Kit, supplied by Fisher Scientific, 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/infinity cholesterol liquid stable reagent kit/product/Fisher Scientific
Average 90 stars, based on 1 article reviews
infinity cholesterol liquid stable reagent kit - by Bioz Stars, 2026-05
90/100 stars

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98
Thermo Fisher infinity cholesterol liquid stable reagent kit
( A ) Experimental design. Apoe -/- male mice were fed WD and received drinking water with no additives (Ctrl) or water supplemented with glutamine (Gln), or alpha-ketoglutarate (AKG) for 8 weeks. ( B ) Oil red O analysis of plaque burden in the aorta with ( C ) representative images of aortas from male mice. Scale bar: 2 mm. ( D ) Plaque area at 7 locations across the aortic root from the first appearance of the aortic valves in (top) male and (bottom) female mice. ( E ) Representative images of aortic root plaques from male and female mice in control (Ctrl) and glutamine (Gln) group. Scale bar: 200 μm. Black dashed line marks representative plaques boundaries. ( F ) Total plaque volume in the aortic root, calculated as the area under the curve from (D). ( G ) Sirius red analysis of plaque collagen content. ( H ) Necrotic core size analysis at the point of peak stenosis. ( I ) Plasma <t>cholesterol.</t> ( J ) Glutamine plasma concentration normalized to sex matched controls. (B, F, G, I, J) Data analyzed using one-way ANOVA with Dunnett’s correction or (H) Kruskal Wallis with Dunn’s correction for post-hoc analysis with N ≥ 13. Error bars represent mean ± SEM or (H) median ± IQR. *** P < 0.001; ** P = 0.001 to 0.01; * P = 0.01 to 0.05; ns, not significant.
Infinity Cholesterol Liquid Stable Reagent Kit, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/infinity cholesterol liquid stable reagent kit/product/Thermo Fisher
Average 98 stars, based on 1 article reviews
infinity cholesterol liquid stable reagent kit - by Bioz Stars, 2026-05
98/100 stars
  Buy from Supplier

90
Fisher Scientific infinity cholesterol liquid stable reagent kit
( A ) Experimental design. Apoe -/- male mice were fed WD and received drinking water with no additives (Ctrl) or water supplemented with glutamine (Gln), or alpha-ketoglutarate (AKG) for 8 weeks. ( B ) Oil red O analysis of plaque burden in the aorta with ( C ) representative images of aortas from male mice. Scale bar: 2 mm. ( D ) Plaque area at 7 locations across the aortic root from the first appearance of the aortic valves in (top) male and (bottom) female mice. ( E ) Representative images of aortic root plaques from male and female mice in control (Ctrl) and glutamine (Gln) group. Scale bar: 200 μm. Black dashed line marks representative plaques boundaries. ( F ) Total plaque volume in the aortic root, calculated as the area under the curve from (D). ( G ) Sirius red analysis of plaque collagen content. ( H ) Necrotic core size analysis at the point of peak stenosis. ( I ) Plasma <t>cholesterol.</t> ( J ) Glutamine plasma concentration normalized to sex matched controls. (B, F, G, I, J) Data analyzed using one-way ANOVA with Dunnett’s correction or (H) Kruskal Wallis with Dunn’s correction for post-hoc analysis with N ≥ 13. Error bars represent mean ± SEM or (H) median ± IQR. *** P < 0.001; ** P = 0.001 to 0.01; * P = 0.01 to 0.05; ns, not significant.
Infinity Cholesterol Liquid Stable Reagent Kit, supplied by Fisher Scientific, 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/infinity cholesterol liquid stable reagent kit/product/Fisher Scientific
Average 90 stars, based on 1 article reviews
infinity cholesterol liquid stable reagent kit - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier

99
Thermo Fisher infinity cholesterol liquid stable reagent commercial kits
( A ) Experimental design. Apoe -/- male mice were fed WD and received drinking water with no additives (Ctrl) or water supplemented with glutamine (Gln), or alpha-ketoglutarate (AKG) for 8 weeks. ( B ) Oil red O analysis of plaque burden in the aorta with ( C ) representative images of aortas from male mice. Scale bar: 2 mm. ( D ) Plaque area at 7 locations across the aortic root from the first appearance of the aortic valves in (top) male and (bottom) female mice. ( E ) Representative images of aortic root plaques from male and female mice in control (Ctrl) and glutamine (Gln) group. Scale bar: 200 μm. Black dashed line marks representative plaques boundaries. ( F ) Total plaque volume in the aortic root, calculated as the area under the curve from (D). ( G ) Sirius red analysis of plaque collagen content. ( H ) Necrotic core size analysis at the point of peak stenosis. ( I ) Plasma <t>cholesterol.</t> ( J ) Glutamine plasma concentration normalized to sex matched controls. (B, F, G, I, J) Data analyzed using one-way ANOVA with Dunnett’s correction or (H) Kruskal Wallis with Dunn’s correction for post-hoc analysis with N ≥ 13. Error bars represent mean ± SEM or (H) median ± IQR. *** P < 0.001; ** P = 0.001 to 0.01; * P = 0.01 to 0.05; ns, not significant.
Infinity Cholesterol Liquid Stable Reagent Commercial Kits, 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/result/infinity cholesterol liquid stable reagent commercial kits/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
infinity cholesterol liquid stable reagent commercial kits - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier

99
Thermo Fisher infinity cholesterol liquid stable reagent kits
Metabolic parameters in control and LivDgat2KO mice on chow and FPC diets. (A) LivDgat2KO and control mice have similar body weights on chow or FPC diet for 16 weeks. Liver to body weight is lower in LivDgat2KO animals fed the FPC diet. Age 24 weeks, n = 7–10/genotype on chow diet, n = 10 females/genotype on FPC, 15–18 males/genotype on FPC. (B) Glucose and insulin tolerance tests performed in mice fed an FPC diet for 14–15 weeks. For GTT, mice were fasted overnight, then 2 mg/g of glucose was administered intraperitoneally, and blood glucose measured at times as indicated. For ITT, mice were fasted for 4 hours, then 1 U/kg of insulin was administered intraperitoneally, and blood glucose measured at times as indicated. n = 9–13 males/genotype, n = 8–15 females/genotype. (C) Plasma TG, <t>cholesterol</t> (Chol), and HDL-C levels in mice fed chow or FPC diets for 16 weeks. n = 5 males/genotype, n = 4–5 females/genotype on chow diet. n = 11–16 males/genotype, n = 7 females/genotype on FPC diet. (D) Plasma TG levels. After a 4-hour fast, mice were administered Tyloxapol at time 0 and subsequent TG levels were measured at indicated time points. n = 6 males/genotype, n = 5 females/genotype. (E) Real-time PCR analysis of apolipoprotein genes in mice on chow and FPC diets. Apoa1 gene expression is decreased in LivDgat2KO animals on FPC diet. n = 4–5 females and males/genotype on chow, n = 10 females/genotype, 15–18 males/genotype on FPC. (F) Immunoblotting showing less apo-A1 in plasma of male mice on an FPC diet. Ponceau stain, with albumin band, of the same blotting is also shown. n = 4/genotype. *Indicates statistical difference between diets, *P < 0.05; **P < 0.005; ***P < 0.0005; ****P < 0.0001. +Indicates statistical difference between genotypes, +P < 0.05; ++P < 0.005; +++P < 0.0005; ++++P < 0.0001. Abbreviations: GTT, glucose tolerance test; ITT, insulin tolerance test.
Infinity Cholesterol Liquid Stable Reagent Kits, 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/result/infinity cholesterol liquid stable reagent kits/product/Thermo Fisher
Average 99 stars, based on 1 article reviews
infinity cholesterol liquid stable reagent kits - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier

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( A ) Experimental design. Apoe -/- male mice were fed WD and received drinking water with no additives (Ctrl) or water supplemented with glutamine (Gln), or alpha-ketoglutarate (AKG) for 8 weeks. ( B ) Oil red O analysis of plaque burden in the aorta with ( C ) representative images of aortas from male mice. Scale bar: 2 mm. ( D ) Plaque area at 7 locations across the aortic root from the first appearance of the aortic valves in (top) male and (bottom) female mice. ( E ) Representative images of aortic root plaques from male and female mice in control (Ctrl) and glutamine (Gln) group. Scale bar: 200 μm. Black dashed line marks representative plaques boundaries. ( F ) Total plaque volume in the aortic root, calculated as the area under the curve from (D). ( G ) Sirius red analysis of plaque collagen content. ( H ) Necrotic core size analysis at the point of peak stenosis. ( I ) Plasma cholesterol. ( J ) Glutamine plasma concentration normalized to sex matched controls. (B, F, G, I, J) Data analyzed using one-way ANOVA with Dunnett’s correction or (H) Kruskal Wallis with Dunn’s correction for post-hoc analysis with N ≥ 13. Error bars represent mean ± SEM or (H) median ± IQR. *** P < 0.001; ** P = 0.001 to 0.01; * P = 0.01 to 0.05; ns, not significant.

Journal: bioRxiv

Article Title: Dietary depletion of glutamine is atheroprotective

doi: 10.64898/2026.03.06.710174

Figure Lengend Snippet: ( A ) Experimental design. Apoe -/- male mice were fed WD and received drinking water with no additives (Ctrl) or water supplemented with glutamine (Gln), or alpha-ketoglutarate (AKG) for 8 weeks. ( B ) Oil red O analysis of plaque burden in the aorta with ( C ) representative images of aortas from male mice. Scale bar: 2 mm. ( D ) Plaque area at 7 locations across the aortic root from the first appearance of the aortic valves in (top) male and (bottom) female mice. ( E ) Representative images of aortic root plaques from male and female mice in control (Ctrl) and glutamine (Gln) group. Scale bar: 200 μm. Black dashed line marks representative plaques boundaries. ( F ) Total plaque volume in the aortic root, calculated as the area under the curve from (D). ( G ) Sirius red analysis of plaque collagen content. ( H ) Necrotic core size analysis at the point of peak stenosis. ( I ) Plasma cholesterol. ( J ) Glutamine plasma concentration normalized to sex matched controls. (B, F, G, I, J) Data analyzed using one-way ANOVA with Dunnett’s correction or (H) Kruskal Wallis with Dunn’s correction for post-hoc analysis with N ≥ 13. Error bars represent mean ± SEM or (H) median ± IQR. *** P < 0.001; ** P = 0.001 to 0.01; * P = 0.01 to 0.05; ns, not significant.

Article Snippet: Plasma cholesterol was analyzed, using Infinity Cholesterol Liquid Stable Reagent kit (Thermo Scientific; cat#: TR13421) and Data-Trol A, Abnormal Control Serum (Thermo Scientific; cat#: TR41001), as an internal standard, according to the manufacturer’s instructions.

Techniques: Control, Clinical Proteomics, Concentration Assay

Metabolic parameters in control and LivDgat2KO mice on chow and FPC diets. (A) LivDgat2KO and control mice have similar body weights on chow or FPC diet for 16 weeks. Liver to body weight is lower in LivDgat2KO animals fed the FPC diet. Age 24 weeks, n = 7–10/genotype on chow diet, n = 10 females/genotype on FPC, 15–18 males/genotype on FPC. (B) Glucose and insulin tolerance tests performed in mice fed an FPC diet for 14–15 weeks. For GTT, mice were fasted overnight, then 2 mg/g of glucose was administered intraperitoneally, and blood glucose measured at times as indicated. For ITT, mice were fasted for 4 hours, then 1 U/kg of insulin was administered intraperitoneally, and blood glucose measured at times as indicated. n = 9–13 males/genotype, n = 8–15 females/genotype. (C) Plasma TG, cholesterol (Chol), and HDL-C levels in mice fed chow or FPC diets for 16 weeks. n = 5 males/genotype, n = 4–5 females/genotype on chow diet. n = 11–16 males/genotype, n = 7 females/genotype on FPC diet. (D) Plasma TG levels. After a 4-hour fast, mice were administered Tyloxapol at time 0 and subsequent TG levels were measured at indicated time points. n = 6 males/genotype, n = 5 females/genotype. (E) Real-time PCR analysis of apolipoprotein genes in mice on chow and FPC diets. Apoa1 gene expression is decreased in LivDgat2KO animals on FPC diet. n = 4–5 females and males/genotype on chow, n = 10 females/genotype, 15–18 males/genotype on FPC. (F) Immunoblotting showing less apo-A1 in plasma of male mice on an FPC diet. Ponceau stain, with albumin band, of the same blotting is also shown. n = 4/genotype. *Indicates statistical difference between diets, *P < 0.05; **P < 0.005; ***P < 0.0005; ****P < 0.0001. +Indicates statistical difference between genotypes, +P < 0.05; ++P < 0.005; +++P < 0.0005; ++++P < 0.0001. Abbreviations: GTT, glucose tolerance test; ITT, insulin tolerance test.

Journal: Hepatology (Baltimore, Md.)

Article Title: Hepatocyte Deletion of Triglyceride-Synthesis Enzyme Acyl CoA: Diacylglycerol Acyltransferase 2 Reduces Steatosis Without Increasing Inflammation or Fibrosis in Mice

doi: 10.1002/hep.30765

Figure Lengend Snippet: Metabolic parameters in control and LivDgat2KO mice on chow and FPC diets. (A) LivDgat2KO and control mice have similar body weights on chow or FPC diet for 16 weeks. Liver to body weight is lower in LivDgat2KO animals fed the FPC diet. Age 24 weeks, n = 7–10/genotype on chow diet, n = 10 females/genotype on FPC, 15–18 males/genotype on FPC. (B) Glucose and insulin tolerance tests performed in mice fed an FPC diet for 14–15 weeks. For GTT, mice were fasted overnight, then 2 mg/g of glucose was administered intraperitoneally, and blood glucose measured at times as indicated. For ITT, mice were fasted for 4 hours, then 1 U/kg of insulin was administered intraperitoneally, and blood glucose measured at times as indicated. n = 9–13 males/genotype, n = 8–15 females/genotype. (C) Plasma TG, cholesterol (Chol), and HDL-C levels in mice fed chow or FPC diets for 16 weeks. n = 5 males/genotype, n = 4–5 females/genotype on chow diet. n = 11–16 males/genotype, n = 7 females/genotype on FPC diet. (D) Plasma TG levels. After a 4-hour fast, mice were administered Tyloxapol at time 0 and subsequent TG levels were measured at indicated time points. n = 6 males/genotype, n = 5 females/genotype. (E) Real-time PCR analysis of apolipoprotein genes in mice on chow and FPC diets. Apoa1 gene expression is decreased in LivDgat2KO animals on FPC diet. n = 4–5 females and males/genotype on chow, n = 10 females/genotype, 15–18 males/genotype on FPC. (F) Immunoblotting showing less apo-A1 in plasma of male mice on an FPC diet. Ponceau stain, with albumin band, of the same blotting is also shown. n = 4/genotype. *Indicates statistical difference between diets, *P < 0.05; **P < 0.005; ***P < 0.0005; ****P < 0.0001. +Indicates statistical difference between genotypes, +P < 0.05; ++P < 0.005; +++P < 0.0005; ++++P < 0.0001. Abbreviations: GTT, glucose tolerance test; ITT, insulin tolerance test.

Article Snippet: TG and cholesterol were measured using Infinity Triglycerides Liquid Stable Reagent and Infinity Cholesterol Liquid Stable Reagent kits (Thermo Fisher Scientific).

Techniques: Control, Clinical Proteomics, Real-time Polymerase Chain Reaction, Gene Expression, Western Blot, Staining

LivDgat2KO mice have improved steatosis on FPC diet. (A) Representative ORO-stained liver sections and steatosis severity scores in mice on FPC diet for 16 weeks. Each symbol represents the score for an individual mouse. n = 10 females/genotype, 15–18 males/genotype. (B) Hepatic TG and total cholesterol content in mice on FPC diet for 16 weeks. n = 8/genotype/sex. (C) Real-time PCR analysis of TG synthesis genes, Dgat1 and Dgat2 in this cohort. (D) De novo lipogenesis gene expression measured by qPCR and relative protein amounts detected by mass spectrometry in mice on chow and FPC diets. (E) Beta-oxidation gene expression measured by qPCR and relative protein amounts detected by mass spectrometry in mice on chow and FPC diets. n = 4–5 females and males/genotype on chow. n = 10 females/genotype, 15–18 males/genotype on FPC for gene expression data. n = 3 males/genotype/diet for proteomic data. *Indicates statistical difference between diets, *P < 0.05; **P < 0.005; ****P < 0.0001. +Indicates statistical difference between genotypes, +P < 0.05; ++P < 0.005; +++P < 0.0005; ++++P < 0.0001. Abbreviations: Acac, acyl-CoA carboxylase; Acadl, acyl-CoA dehydrogenase long chain; Acadm, acyl-CoA dehydrogenase medium chain; Acox, acyl Co-A oxidase; CV, central vein; Chol, cholesterol; Fasn, fatty acid synthase; Ppargc1α, peroxisome proliferator-activated receptor γ co-activator 1α; PT, portal triad.

Journal: Hepatology (Baltimore, Md.)

Article Title: Hepatocyte Deletion of Triglyceride-Synthesis Enzyme Acyl CoA: Diacylglycerol Acyltransferase 2 Reduces Steatosis Without Increasing Inflammation or Fibrosis in Mice

doi: 10.1002/hep.30765

Figure Lengend Snippet: LivDgat2KO mice have improved steatosis on FPC diet. (A) Representative ORO-stained liver sections and steatosis severity scores in mice on FPC diet for 16 weeks. Each symbol represents the score for an individual mouse. n = 10 females/genotype, 15–18 males/genotype. (B) Hepatic TG and total cholesterol content in mice on FPC diet for 16 weeks. n = 8/genotype/sex. (C) Real-time PCR analysis of TG synthesis genes, Dgat1 and Dgat2 in this cohort. (D) De novo lipogenesis gene expression measured by qPCR and relative protein amounts detected by mass spectrometry in mice on chow and FPC diets. (E) Beta-oxidation gene expression measured by qPCR and relative protein amounts detected by mass spectrometry in mice on chow and FPC diets. n = 4–5 females and males/genotype on chow. n = 10 females/genotype, 15–18 males/genotype on FPC for gene expression data. n = 3 males/genotype/diet for proteomic data. *Indicates statistical difference between diets, *P < 0.05; **P < 0.005; ****P < 0.0001. +Indicates statistical difference between genotypes, +P < 0.05; ++P < 0.005; +++P < 0.0005; ++++P < 0.0001. Abbreviations: Acac, acyl-CoA carboxylase; Acadl, acyl-CoA dehydrogenase long chain; Acadm, acyl-CoA dehydrogenase medium chain; Acox, acyl Co-A oxidase; CV, central vein; Chol, cholesterol; Fasn, fatty acid synthase; Ppargc1α, peroxisome proliferator-activated receptor γ co-activator 1α; PT, portal triad.

Article Snippet: TG and cholesterol were measured using Infinity Triglycerides Liquid Stable Reagent and Infinity Cholesterol Liquid Stable Reagent kits (Thermo Fisher Scientific).

Techniques: Staining, Real-time Polymerase Chain Reaction, Gene Expression, Mass Spectrometry

Summary of lipid class changes in LivDgat2KO mice fed an FPC diet. (A) Changes in lipid class abundance and palmitate content of lipids. Data are displayed as fold change compared to chow-fed control mice (Chow Control). Bold in lower left panel indicates significant difference between Chow Control and FPC Control. Bold Italic indicates significant difference between genotypes. (B) Change in cholesterol esters between the groups, compared to chow-fed control mice. N = 4–5 male mice/group. *Indicates statistical difference between diets, ****P < 0.0001. +Indicates statistical difference between genotypes, ++++P < 0.0001. Abbreviations: G3P, glycerol 3-phosphate; LCB, long-chain sphingoid bases; Cer, ceramide; SM, sphingomyelin; LPA, lysophosphatidic acid; PA, phosphatidic acid; DAG, diacylglycerol; TAG, triglyceride; PC, phosphatidylcholine; LPC, lysophophatidylcholine; PE, phosphatidylethanolamine; LPE, lysophosphatidylethanolamine; CDP-DAG, cytidine diphosphate diacylglycerol; PI, phosphatidylinositol; LPI, lysophosphatidylinositol; PG, phosphatidylglycerol; LPG, lysophosphatidylglycerol; PS, phosphatidylserine; LPS, lysophosphatidylserine.

Journal: Hepatology (Baltimore, Md.)

Article Title: Hepatocyte Deletion of Triglyceride-Synthesis Enzyme Acyl CoA: Diacylglycerol Acyltransferase 2 Reduces Steatosis Without Increasing Inflammation or Fibrosis in Mice

doi: 10.1002/hep.30765

Figure Lengend Snippet: Summary of lipid class changes in LivDgat2KO mice fed an FPC diet. (A) Changes in lipid class abundance and palmitate content of lipids. Data are displayed as fold change compared to chow-fed control mice (Chow Control). Bold in lower left panel indicates significant difference between Chow Control and FPC Control. Bold Italic indicates significant difference between genotypes. (B) Change in cholesterol esters between the groups, compared to chow-fed control mice. N = 4–5 male mice/group. *Indicates statistical difference between diets, ****P < 0.0001. +Indicates statistical difference between genotypes, ++++P < 0.0001. Abbreviations: G3P, glycerol 3-phosphate; LCB, long-chain sphingoid bases; Cer, ceramide; SM, sphingomyelin; LPA, lysophosphatidic acid; PA, phosphatidic acid; DAG, diacylglycerol; TAG, triglyceride; PC, phosphatidylcholine; LPC, lysophophatidylcholine; PE, phosphatidylethanolamine; LPE, lysophosphatidylethanolamine; CDP-DAG, cytidine diphosphate diacylglycerol; PI, phosphatidylinositol; LPI, lysophosphatidylinositol; PG, phosphatidylglycerol; LPG, lysophosphatidylglycerol; PS, phosphatidylserine; LPS, lysophosphatidylserine.

Article Snippet: TG and cholesterol were measured using Infinity Triglycerides Liquid Stable Reagent and Infinity Cholesterol Liquid Stable Reagent kits (Thermo Fisher Scientific).

Techniques: Control