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high density lipoprotein cholesterol hdl c  (Randox)


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    Randox high density lipoprotein cholesterol hdl c
    High Density Lipoprotein Cholesterol Hdl C, supplied by Randox, used in various techniques. Bioz Stars score: 96/100, based on 795 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/high+density+lipoprotein+cholesterol+hdl+c/LIPOPROTEIN/pm42036000-108-7-15
    Average 96 stars, based on 795 article reviews
    high density lipoprotein cholesterol hdl c - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Clinical Proteomics:

    Article Title: Modulation of molecular and serological biomarkers by (-)-epicatechin consumption on a murine model of metabolic dysfunction-associated steatotic liver disease.
    Article Snippet: Metabolic dysfunction-associated steatotic liver disease (MASLD) represents the most common liver disease worldwide.. MASLD often goes undiagnosed or is not treated with specific medications.. Therefore, new alternative treatments that help reverse or prevent the progression of this pathology need to be explored.

    Article Title: Dose–Response Effect of Watermelon Consumption on Ambulatory Blood Pressure in Adults with Elevated Blood Pressure: A Randomized Controlled Pilot Trial
    Article Snippet: .. Plasma was analyzed for glucose, insulin, triglycerides (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C) using an RX Daytona automated clinical analyzer (Randox Laboratories, Crumlin, UK) with appropriate internal and external control samples. ..

    Article Title: The Effects of Aqueous Extract of Garcinia kola on Hematological Parameters and Lipid Profile in Female Sprague-Dawley Rats
    Article Snippet: From the blood samples, the Hematological Parameters were determined using the automated hematologic analyzer SYSMEX KX21, a product of SYSMEX Corporation, Japan employing the methods described by Dacie and Lewis.18 .. Plasma analysis for total cholesterol (TC), triglycerides (TAG), and high density lipoprotein cholesterol (HDL-C) were determined by enzymatic method coupled with spectrophotometry using assay kit (Randox Lab. Ltd., Co. Antrim, UK). ..

    Article Title: Dose–Response Effect of Watermelon Consumption on Ambulatory Blood Pressure in Adults with Elevated Blood Pressure: A Randomized Controlled Pilot Trial
    Article Snippet: .. Plasma was analyzed for glucose, insulin, triglycerides (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C) using an RX Daytona automated clinical analyzer (Randox Laboratories, Crumlin, UK) with appropriate internal and external control samples. ..

    Control:

    Article Title: Dose–Response Effect of Watermelon Consumption on Ambulatory Blood Pressure in Adults with Elevated Blood Pressure: A Randomized Controlled Pilot Trial
    Article Snippet: .. Plasma was analyzed for glucose, insulin, triglycerides (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C) using an RX Daytona automated clinical analyzer (Randox Laboratories, Crumlin, UK) with appropriate internal and external control samples. ..

    Article Title: Dose–Response Effect of Watermelon Consumption on Ambulatory Blood Pressure in Adults with Elevated Blood Pressure: A Randomized Controlled Pilot Trial
    Article Snippet: .. Plasma was analyzed for glucose, insulin, triglycerides (TG), total cholesterol (TC), and high-density lipoprotein cholesterol (HDL-C) using an RX Daytona automated clinical analyzer (Randox Laboratories, Crumlin, UK) with appropriate internal and external control samples. ..

    Spectrophotometry:

    Article Title: The Effects of Aqueous Extract of Garcinia kola on Hematological Parameters and Lipid Profile in Female Sprague-Dawley Rats
    Article Snippet: From the blood samples, the Hematological Parameters were determined using the automated hematologic analyzer SYSMEX KX21, a product of SYSMEX Corporation, Japan employing the methods described by Dacie and Lewis.18 .. Plasma analysis for total cholesterol (TC), triglycerides (TAG), and high density lipoprotein cholesterol (HDL-C) were determined by enzymatic method coupled with spectrophotometry using assay kit (Randox Lab. Ltd., Co. Antrim, UK). ..

    Diagnostic Assay:

    Article Title: Seed oil of Chrysophyllum albidum G. Don. demonstrated antioxidant and anti-inflammatory effects in experimental rodent models through suppression of pro-inflammatory cytokines and enhanced expression of Nrf2.
    Article Snippet: Ethnopharmacology relevance: The seed of the African cherry, Chrysophyllum albidum is well-known for its use in ethnomedicine for malaria, yellow fever, stomach ache and inflammatory disorders.. Aim of the study: This study investigated the antioxidant and anti-inflammatory potential of Chrysophyllum albidum Seed Oil (CASO) in rodent models of carrageenan-induced acute inflammation and Complete Freund's Adjuvant (CFA)-induced arthritis.. Materials and methods: The phytochemical profile of n-hexane seed oil from C. albidum was determined via GC-MS following Soxhlet extraction.

    Article Title: Comparative metabolic effects of a commercial energy drink and a standardized kolanut drink in male rats.
    Article Snippet: Excessive consumption of energy drinks (EDs) has been associated with cardiovascular, metabolic, hepatic, and renal disturbances.. This study compared the metabolic effects of a commercially available energy drink (CED) with a standardized kolanut drink (KD), formulated from kolanut extract and pineapple juice, using caffeinedose–matched conditions to address the lack of direct comparative data in previous literature.. Twenty-eight male Wistar rats were randomized into four groups and treated orally for 56 days: Control, CED (10 mg caffeine/kg bw), KD1 (10 mg caffeine/kg bw), and KD2 (15 mg caffeine/kg bw).

    other:

    Article Title: Honey-Conjugated Honeybee Brood Biopeptides Improve Gastrointestinal Stability, Antioxidant Capacity, and Alleviate Diet-Induced Metabolic Syndrome in a Rat Model
    Article Snippet: The levels of total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) were measured using an automated analyzer (Randox Laboratories, Crumlin, UK) following the manufacturer’s instructions.

    Filtration:

    Article Title: Prevalence of Frailty and Associated Sociodemographic, Biomedical, and Biochemical Factors Amongst Participants Residing in Limpopo Province, South Africa
    Article Snippet: .. Biochemical parameters, including total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), glucose, insulin, albumin-to-creatinine ratio (ACR), and estimated glomerular filtration rate (eGFR), were analyzed using a Randox Plus clinical chemistry analyzer (UK). ..



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    Experimental design, growth, intake partitioning, skeletal-muscle S6 signaling, and endpoint plasma markers under phase-shifted BCAA regimens. (A) Simplified study design: rats were maintained on a 12-h light:12-h dark cycle and assigned for 12 weeks to Ctrl (AIN-93G throughout), D + N − (BCAA+20 during the light/inactive phase and BCAA−20 during the dark/active phase), or D − N + (BCAA−20 during the light/inactive phase and BCAA+20 during the dark/active phase), where BCAA+20 and BCAA−20 denote diets containing ~20% higher or lower total BCAA content than Ctrl, respectively; daily energy and nitrogen were intended to be matched while allowing minor day-to-day variation during implementation ( n = 6/group). (B,C) Individual body weight trajectories from week 0 (acclimation) to weeks 1–12 (experimental period) (B) and weekly body weight distributions shown as boxplots (weeks 1–12) with pairwise between-group comparisons annotated above brackets (C) . (D,E) Representative immunoblots of total ribosomal protein S6 and phosphorylated S6 (p-S6, Ser235/236) in skeletal muscle at the end of the study, with total protein staining (TPS; Ponceau S) used for normalization ( n = 4/group; region approximately ~32 kDa displayed) (D) , and densitometric quantification of S6/TPS, p-S6/TPS, and phosphorylation ratio (p-S6/S6 computed as (p-S6/TPS)/(S6/TPS)) with individual animals overlaid (E) . (F) Weekly feed intake partitioned by circadian phase (inactive/light phase: 07:00–19:00; active/dark phase: 19:00–07:00); within each week, upper brackets/ p -values compare whole-day (24 h) total intake between the groups, and lower brackets/ p -values compare inactive vs. active intake within each group (red p-values indicate p < 0.05 as displayed). (G) Endpoint fasting plasma <t>HDL-C,</t> LDL-C, triglycerides (TG), total cholesterol (TC), and malondialdehyde (MDA) across the groups (units as indicated on axes). Group colors follow Ctrl (red), D − N + (green), and D + N − (blue). Boxplots show median and interquartile range (IQR), whiskers extend to 1.5 × IQR, and points indicate individual values (with outliers beyond whiskers where shown). Pairwise statistics were computed using two-sided t-tests with Holm p -value adjustment.
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    https://www.bioz.com/product/high+density+lipoprotein+cholesterol+hdl+c/High-density+Lipoprotein+Cholesterol+(HDL-C)+Colorimetric+Assay+Kit/pmc13102662-76-31-36
    Average 95 stars, based on 1 article reviews
    hdl c colorimetric assay kits - by Bioz Stars, 2026-10
    95/100 stars
    		  Buy from Supplier

    Image Search Results


    Experimental design, growth, intake partitioning, skeletal-muscle S6 signaling, and endpoint plasma markers under phase-shifted BCAA regimens. (A) Simplified study design: rats were maintained on a 12-h light:12-h dark cycle and assigned for 12 weeks to Ctrl (AIN-93G throughout), D + N − (BCAA+20 during the light/inactive phase and BCAA−20 during the dark/active phase), or D − N + (BCAA−20 during the light/inactive phase and BCAA+20 during the dark/active phase), where BCAA+20 and BCAA−20 denote diets containing ~20% higher or lower total BCAA content than Ctrl, respectively; daily energy and nitrogen were intended to be matched while allowing minor day-to-day variation during implementation ( n = 6/group). (B,C) Individual body weight trajectories from week 0 (acclimation) to weeks 1–12 (experimental period) (B) and weekly body weight distributions shown as boxplots (weeks 1–12) with pairwise between-group comparisons annotated above brackets (C) . (D,E) Representative immunoblots of total ribosomal protein S6 and phosphorylated S6 (p-S6, Ser235/236) in skeletal muscle at the end of the study, with total protein staining (TPS; Ponceau S) used for normalization ( n = 4/group; region approximately ~32 kDa displayed) (D) , and densitometric quantification of S6/TPS, p-S6/TPS, and phosphorylation ratio (p-S6/S6 computed as (p-S6/TPS)/(S6/TPS)) with individual animals overlaid (E) . (F) Weekly feed intake partitioned by circadian phase (inactive/light phase: 07:00–19:00; active/dark phase: 19:00–07:00); within each week, upper brackets/ p -values compare whole-day (24 h) total intake between the groups, and lower brackets/ p -values compare inactive vs. active intake within each group (red p-values indicate p < 0.05 as displayed). (G) Endpoint fasting plasma HDL-C, LDL-C, triglycerides (TG), total cholesterol (TC), and malondialdehyde (MDA) across the groups (units as indicated on axes). Group colors follow Ctrl (red), D − N + (green), and D + N − (blue). Boxplots show median and interquartile range (IQR), whiskers extend to 1.5 × IQR, and points indicate individual values (with outliers beyond whiskers where shown). Pairwise statistics were computed using two-sided t-tests with Holm p -value adjustment.

    Journal: Frontiers in Nutrition

    Article Title: Redistribution of branched-chain amino acid intake between active and inactive phases modulates hepatic metabolism in rats

    doi: 10.3389/fnut.2026.1754879

    Figure Lengend Snippet: Experimental design, growth, intake partitioning, skeletal-muscle S6 signaling, and endpoint plasma markers under phase-shifted BCAA regimens. (A) Simplified study design: rats were maintained on a 12-h light:12-h dark cycle and assigned for 12 weeks to Ctrl (AIN-93G throughout), D + N − (BCAA+20 during the light/inactive phase and BCAA−20 during the dark/active phase), or D − N + (BCAA−20 during the light/inactive phase and BCAA+20 during the dark/active phase), where BCAA+20 and BCAA−20 denote diets containing ~20% higher or lower total BCAA content than Ctrl, respectively; daily energy and nitrogen were intended to be matched while allowing minor day-to-day variation during implementation ( n = 6/group). (B,C) Individual body weight trajectories from week 0 (acclimation) to weeks 1–12 (experimental period) (B) and weekly body weight distributions shown as boxplots (weeks 1–12) with pairwise between-group comparisons annotated above brackets (C) . (D,E) Representative immunoblots of total ribosomal protein S6 and phosphorylated S6 (p-S6, Ser235/236) in skeletal muscle at the end of the study, with total protein staining (TPS; Ponceau S) used for normalization ( n = 4/group; region approximately ~32 kDa displayed) (D) , and densitometric quantification of S6/TPS, p-S6/TPS, and phosphorylation ratio (p-S6/S6 computed as (p-S6/TPS)/(S6/TPS)) with individual animals overlaid (E) . (F) Weekly feed intake partitioned by circadian phase (inactive/light phase: 07:00–19:00; active/dark phase: 19:00–07:00); within each week, upper brackets/ p -values compare whole-day (24 h) total intake between the groups, and lower brackets/ p -values compare inactive vs. active intake within each group (red p-values indicate p < 0.05 as displayed). (G) Endpoint fasting plasma HDL-C, LDL-C, triglycerides (TG), total cholesterol (TC), and malondialdehyde (MDA) across the groups (units as indicated on axes). Group colors follow Ctrl (red), D − N + (green), and D + N − (blue). Boxplots show median and interquartile range (IQR), whiskers extend to 1.5 × IQR, and points indicate individual values (with outliers beyond whiskers where shown). Pairwise statistics were computed using two-sided t-tests with Holm p -value adjustment.

    Article Snippet: Specifically, serum lipids were quantified by measuring total cholesterol (TC) using the Total Cholesterol (TC) Colorimetric Assay kits from Elabscience (Wuhan, China) (catalog no. E-BC-K109-M), high-density lipoprotein cholesterol (HDL-C) using the HDL-C Colorimetric Assay kits from Elabscience (Wuhan, China) (catalog no. E-BC-K221-M), low-density lipoprotein cholesterol (LDL-C) using the LDL-C Colorimetric Assay kits from Elabscience (Wuhan, China) (catalog no. E-BC-K205-M), malondialdehyde (MDA) using the Malondialdehyde (MDA) Colorimetric Assay kits from Elabscience (Wuhan, China) (catalog no. E-BC-K025-M), and triglycerides (TGs) using the Triglyceride (TG) Colorimetric Assay kits from Elabscience (Wuhan, China) (catalog no. E-BC-K261-M).

    Techniques: Clinical Proteomics, Western Blot, Staining, Phospho-proteomics