rat mouse insulin elisa assay kit  (Millipore)


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    Structured Review

    Millipore rat mouse insulin elisa assay kit
    Rat Mouse Insulin Elisa Assay Kit, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat mouse insulin elisa assay kit/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rat mouse insulin elisa assay kit - by Bioz Stars, 2020-08
    86/100 stars

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    Related Articles

    Enzyme-linked Immunosorbent Assay:

    Article Title: Early-onset metabolic syndrome in mice lacking the intestinal uric acid transporter SLC2A9
    Article Snippet: .. Serum and urine uric acid, serum and hepatic cholesterol, TG, FFA and serum insulin were measured using the following kits precisely per manufacturer instructions , , : Amplex Red Uric Acid Assay Kit (Invitrogen, Carlsbad, CA), Infinity Cholesterol Assay Kit, (Thermo Scientific, Waltham, MA), Infinity triglyceride assay kit (Thermo Scientific, Waltham, MA), NEFA free fatty acid determination kit (Wako Diagnostics, Richmond, VA) and rat / mouse insulin ELISA assay kit (Millipore, Billerica, MA). ..

    Uric Acid Assay:

    Article Title: Early-onset metabolic syndrome in mice lacking the intestinal uric acid transporter SLC2A9
    Article Snippet: .. Serum and urine uric acid, serum and hepatic cholesterol, TG, FFA and serum insulin were measured using the following kits precisely per manufacturer instructions , , : Amplex Red Uric Acid Assay Kit (Invitrogen, Carlsbad, CA), Infinity Cholesterol Assay Kit, (Thermo Scientific, Waltham, MA), Infinity triglyceride assay kit (Thermo Scientific, Waltham, MA), NEFA free fatty acid determination kit (Wako Diagnostics, Richmond, VA) and rat / mouse insulin ELISA assay kit (Millipore, Billerica, MA). ..

    Cholesterol Assay:

    Article Title: Early-onset metabolic syndrome in mice lacking the intestinal uric acid transporter SLC2A9
    Article Snippet: .. Serum and urine uric acid, serum and hepatic cholesterol, TG, FFA and serum insulin were measured using the following kits precisely per manufacturer instructions , , : Amplex Red Uric Acid Assay Kit (Invitrogen, Carlsbad, CA), Infinity Cholesterol Assay Kit, (Thermo Scientific, Waltham, MA), Infinity triglyceride assay kit (Thermo Scientific, Waltham, MA), NEFA free fatty acid determination kit (Wako Diagnostics, Richmond, VA) and rat / mouse insulin ELISA assay kit (Millipore, Billerica, MA). ..

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    Millipore mouse rat insulin elisa kit
    Circulating levels of <t>IGF-1</t> and FFAs from control, control + Hex, STZ, and STZ + Hex rats. After the STZ or Hex treatment, terminal blood samples were collected. Circulating levels of ( A ) IGF-1 and ( B ) FFAs relative to fat tissue were determined by IGF-1 and FFAs <t>ELISA</t> kits. n = 6 from each group, data are shown as the mean ± SEM. *** p
    Mouse Rat Insulin Elisa Kit, supplied by Millipore, used in various techniques. Bioz Stars score: 88/100, based on 228 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse rat insulin elisa kit/product/Millipore
    Average 88 stars, based on 228 article reviews
    Price from $9.99 to $1999.99
    mouse rat insulin elisa kit - by Bioz Stars, 2020-08
    88/100 stars
      Buy from Supplier

    90
    Millipore rat mouse fgf21 elisa kit
    Hepatocyte and extrahepatocyte peroxisome proliferator-activated receptor α (PPARα) regulate fibroblast growth factor 21 <t>(FGF21),</t> glycaemia and body temperature during fasting. (A and B) Eleven-week-old male mice of the C57Bl/6J background were fed ad libitum or fasted for 24 h, and were killed around the clock from ZT0 to ZT24. (A) Fgf21 mRNA was quantified by qRT-PCR. (B) Quantification of circulating FGF21 levels by <t>ELISA.</t> (C) Twelve-week-old wild-type (WT), PPARα-hepatocyte knockout ( Pparα hep−/− ) and PPARα knockout ( Pparα −/− ) male mice were fed ad libitum or fasted for 16 h and blood was collected at ZT8 (ZT8 fed) or at ZT16 (ZT16 fasted). FGF21 plasma level was determined by ELISA. (D–G) Male mice of WT, Pparα hep−/− and Pparα −/− genotypes were infected with an adenoviral construct containing cDNA of Fgf21 or an empty vector. Mice were sacrificed after a 24 h fasting period at ZT14. (D) Quantification of circulating FGF21 levels by ELISA. (E) Fgf21, G6pd and Scd1 mRNAs were quantified by qRT-PCR. (F) Quantification of hepatic cholesterol esters and triglycerides. (G) Representative pictures of H E staining of liver sections. Scale bars, 100 µm. (H) Plasma glucose level was monitored over a 24 h fasting period from ZT0 to ZT24 in WT, Pparα hep−/− and Pparα −/− mice. (I, J) Plasma glucose (I) and body temperature (J) were determined at ZT0 in fed mice or at ZT0 in mice fasted for 24 h. Data are shown as mean±SEM. *p≤0.05, **p≤0.01, ***p≤0.005.
    Rat Mouse Fgf21 Elisa Kit, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 11 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rat mouse fgf21 elisa kit/product/Millipore
    Average 90 stars, based on 11 article reviews
    Price from $9.99 to $1999.99
    rat mouse fgf21 elisa kit - by Bioz Stars, 2020-08
    90/100 stars
      Buy from Supplier

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    Circulating levels of IGF-1 and FFAs from control, control + Hex, STZ, and STZ + Hex rats. After the STZ or Hex treatment, terminal blood samples were collected. Circulating levels of ( A ) IGF-1 and ( B ) FFAs relative to fat tissue were determined by IGF-1 and FFAs ELISA kits. n = 6 from each group, data are shown as the mean ± SEM. *** p

    Journal: International Journal of Molecular Sciences

    Article Title: Enhanced Pulsatile Growth Hormone Secretion and Altered Metabolic Hormones by in Vivo Hexarelin Treatment in Streptozotocin-Induced Diabetic Rats

    doi: 10.3390/ijms19103067

    Figure Lengend Snippet: Circulating levels of IGF-1 and FFAs from control, control + Hex, STZ, and STZ + Hex rats. After the STZ or Hex treatment, terminal blood samples were collected. Circulating levels of ( A ) IGF-1 and ( B ) FFAs relative to fat tissue were determined by IGF-1 and FFAs ELISA kits. n = 6 from each group, data are shown as the mean ± SEM. *** p

    Article Snippet: Circulating levels of IGF-1, insulin, and FFAs were determined by Mouse/Rat IGF-1 Quantikine ELISA kit (R & D Systems, Minneapolis, MN, USA), Mouse/Rat Insulin ELISA kit (EMD Millipore, St. Charles, MI, USA), and nonesterified fatty acids (NEFA-C) Assay (Wako, Osaka, Japan), respectively.

    Techniques: Enzyme-linked Immunosorbent Assay

    Circulating levels of IGF-1 and FFAs from control, control + Hex, STZ, and STZ + Hex rats. After the STZ or Hex treatment, terminal blood samples were collected. Circulating levels of ( A ) IGF-1 and ( B ) FFAs relative to fat tissue were determined by IGF-1 and FFAs ELISA kits. n = 6 from each group, data are shown as the mean ± SEM. *** p

    Journal: International Journal of Molecular Sciences

    Article Title: Enhanced Pulsatile Growth Hormone Secretion and Altered Metabolic Hormones by in Vivo Hexarelin Treatment in Streptozotocin-Induced Diabetic Rats

    doi: 10.3390/ijms19103067

    Figure Lengend Snippet: Circulating levels of IGF-1 and FFAs from control, control + Hex, STZ, and STZ + Hex rats. After the STZ or Hex treatment, terminal blood samples were collected. Circulating levels of ( A ) IGF-1 and ( B ) FFAs relative to fat tissue were determined by IGF-1 and FFAs ELISA kits. n = 6 from each group, data are shown as the mean ± SEM. *** p

    Article Snippet: Circulating levels of IGF-1, insulin, and FFAs were determined by Mouse/Rat IGF-1 Quantikine ELISA kit (R & D Systems, Minneapolis, MN, USA), Mouse/Rat Insulin ELISA kit (EMD Millipore, St. Charles, MI, USA), and nonesterified fatty acids (NEFA-C) Assay (Wako, Osaka, Japan), respectively.

    Techniques: Enzyme-linked Immunosorbent Assay

    Metformin-induced inhibition of the mTOR pathway in lung tissue is associated with decreases in circulating levels of IGF-1 and insulin a–b) Plasma levels of insulin (a) or IGF-1 (b) were assessed by ELISA in A/J mice treated with oral or intraperitoneal administration of metformin at the end of the tumorigenesis studies. Graphs show mean values and error bars represent SD. This analysis was performed on 5 mice/treatment group. Plasma IGF-1 levels were also assessed in mice given intraperitoneal injections of saline or 250 mg/kg metformin qd x 3 (b, far right panel). (c) Immunoblotting analysis of IGF-1R/IR/Akt/mTOR pathway in liver and lung tissues harvested from A/J mice 0.5 h after administration of 0.5 mg/kg IGF-1 or 0.75 U of insulin.

    Journal: Cancer prevention research (Philadelphia, Pa.)

    Article Title: Metformin prevents tobacco carcinogen-induced lung tumorigenesis

    doi: 10.1158/1940-6207.CAPR-10-0055

    Figure Lengend Snippet: Metformin-induced inhibition of the mTOR pathway in lung tissue is associated with decreases in circulating levels of IGF-1 and insulin a–b) Plasma levels of insulin (a) or IGF-1 (b) were assessed by ELISA in A/J mice treated with oral or intraperitoneal administration of metformin at the end of the tumorigenesis studies. Graphs show mean values and error bars represent SD. This analysis was performed on 5 mice/treatment group. Plasma IGF-1 levels were also assessed in mice given intraperitoneal injections of saline or 250 mg/kg metformin qd x 3 (b, far right panel). (c) Immunoblotting analysis of IGF-1R/IR/Akt/mTOR pathway in liver and lung tissues harvested from A/J mice 0.5 h after administration of 0.5 mg/kg IGF-1 or 0.75 U of insulin.

    Article Snippet: Plasma levels of IGF-1 and insulin were measured using the Mouse/Rat IGF-1 ELISA (Diagnostic Systems Laboratories, Webster, TX) and the Rat/Mouse Insulin ELISA kit (Millipore, Billerica, MA), respectively.

    Techniques: Inhibition, Enzyme-linked Immunosorbent Assay, Mouse Assay

    Hepatocyte and extrahepatocyte peroxisome proliferator-activated receptor α (PPARα) regulate fibroblast growth factor 21 (FGF21), glycaemia and body temperature during fasting. (A and B) Eleven-week-old male mice of the C57Bl/6J background were fed ad libitum or fasted for 24 h, and were killed around the clock from ZT0 to ZT24. (A) Fgf21 mRNA was quantified by qRT-PCR. (B) Quantification of circulating FGF21 levels by ELISA. (C) Twelve-week-old wild-type (WT), PPARα-hepatocyte knockout ( Pparα hep−/− ) and PPARα knockout ( Pparα −/− ) male mice were fed ad libitum or fasted for 16 h and blood was collected at ZT8 (ZT8 fed) or at ZT16 (ZT16 fasted). FGF21 plasma level was determined by ELISA. (D–G) Male mice of WT, Pparα hep−/− and Pparα −/− genotypes were infected with an adenoviral construct containing cDNA of Fgf21 or an empty vector. Mice were sacrificed after a 24 h fasting period at ZT14. (D) Quantification of circulating FGF21 levels by ELISA. (E) Fgf21, G6pd and Scd1 mRNAs were quantified by qRT-PCR. (F) Quantification of hepatic cholesterol esters and triglycerides. (G) Representative pictures of H E staining of liver sections. Scale bars, 100 µm. (H) Plasma glucose level was monitored over a 24 h fasting period from ZT0 to ZT24 in WT, Pparα hep−/− and Pparα −/− mice. (I, J) Plasma glucose (I) and body temperature (J) were determined at ZT0 in fed mice or at ZT0 in mice fasted for 24 h. Data are shown as mean±SEM. *p≤0.05, **p≤0.01, ***p≤0.005.

    Journal: Gut

    Article Title: Liver PPARα is crucial for whole-body fatty acid homeostasis and is protective against NAFLD

    doi: 10.1136/gutjnl-2015-310798

    Figure Lengend Snippet: Hepatocyte and extrahepatocyte peroxisome proliferator-activated receptor α (PPARα) regulate fibroblast growth factor 21 (FGF21), glycaemia and body temperature during fasting. (A and B) Eleven-week-old male mice of the C57Bl/6J background were fed ad libitum or fasted for 24 h, and were killed around the clock from ZT0 to ZT24. (A) Fgf21 mRNA was quantified by qRT-PCR. (B) Quantification of circulating FGF21 levels by ELISA. (C) Twelve-week-old wild-type (WT), PPARα-hepatocyte knockout ( Pparα hep−/− ) and PPARα knockout ( Pparα −/− ) male mice were fed ad libitum or fasted for 16 h and blood was collected at ZT8 (ZT8 fed) or at ZT16 (ZT16 fasted). FGF21 plasma level was determined by ELISA. (D–G) Male mice of WT, Pparα hep−/− and Pparα −/− genotypes were infected with an adenoviral construct containing cDNA of Fgf21 or an empty vector. Mice were sacrificed after a 24 h fasting period at ZT14. (D) Quantification of circulating FGF21 levels by ELISA. (E) Fgf21, G6pd and Scd1 mRNAs were quantified by qRT-PCR. (F) Quantification of hepatic cholesterol esters and triglycerides. (G) Representative pictures of H E staining of liver sections. Scale bars, 100 µm. (H) Plasma glucose level was monitored over a 24 h fasting period from ZT0 to ZT24 in WT, Pparα hep−/− and Pparα −/− mice. (I, J) Plasma glucose (I) and body temperature (J) were determined at ZT0 in fed mice or at ZT0 in mice fasted for 24 h. Data are shown as mean±SEM. *p≤0.05, **p≤0.01, ***p≤0.005.

    Article Snippet: Plasma analysis Plasma FGF21 and insulin, respectively, were assayed using the rat/mouse FGF21 ELISA kit (EMD Millipore) and the ultrasensitive mouse insulin ELISA kit (Crystal Chem) following the manufacturer's instructions.

    Techniques: Mouse Assay, Quantitative RT-PCR, Enzyme-linked Immunosorbent Assay, Knock-Out, Infection, Construct, Plasmid Preparation, Staining