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Insulin elisa kit

Manufactured by Cusabio
Sourced in United States, China

The Insulin ELISA kit is a laboratory equipment designed to quantitatively measure insulin levels in biological samples. It utilizes the enzyme-linked immunosorbent assay (ELISA) technique to detect and quantify insulin concentrations.

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7 protocols using insulin elisa kit

1

Glycemic and Oxidative Stress Markers

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Fructosamine (FTA) level was measured, by ab228558 fructosamine assay kit (Abcam, MA, USA), to detect the average glycemic level over the past three weeks [30 (link), 31 (link)]. Fasting blood glucose (FBG) and serum insulin were measured using ab65333 glucose assay kit (Abcam, MA, USA), and insulin ELISA kit (CSB-E05070r, CUSABIO, Texas, USA). Serum liver function enzymes [alanine aminotransferase (ALT) and aspartate aminotransferase (AST)] were measured by rat ELISA kits (MBS269614, San Diego, California, USA and CSB-E13023r, CUSABIO, Texas, USA; respectively). Serum urea and creatinine were measured by ELISA kits (MBS2600001, San Diego, California, USA and MBS007289, San Diego, California, USA; respectively). Serum malondialdehyde (MDA), superoxide dismutase (SOD) and glutathione peroxidase (GPx) were measured by rat ELISA kits (MBS268427, San Diego, California, USA; MBS266897, San Diego, California, USA and MBS727547, San Diego, California, USA), respectively.
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2

Glucose Tolerance Test in DM/DN Rabbits

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Glucose tolerance was measured using the OGTT assay [28 (link)]. After fasting for 8 h, all DM/DN rabbits were intragastrically fed with 2 g/kg glucose within 2–3 min after receiving different treatments. At 0.5, 1, 1.5, and 2 h time points, a drop of blood was taken from the auricular vein and the blood glucose concentration was measured using a blood glucose meter (Yuwell, Jiangsu, China). The serum INS concentrations were measured using an Insulin ELISA kit (GSB-E05071m, Cusabio, Wuhan, China).
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3

Serum Lipid and Inflammatory Markers

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After finishing the study, all SD rats were sacrificed at once, and serum was collected instantaneously by centrifugation at 1200× g for 15 min. The serum lipid index: total triglycerides (TG), total cholesterol (TC), low-density lipoprotein (LDL), and high-density lipoprotein (HDL) were evaluated the lipid changes. Aspartate and alanine transaminases (AST and ALT) were examined to assess the hepatic injury. All above-mentioned indexes were measured by commercially available kits (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Enzyme-linked immunoassay (ELISA) measurements of serum TNF-α, IL-1β and IL-6 were performed following the user instructions (Neobioscience Technology Co., Ltd., Shenzhen, China). An insulin ELISA kit was purchased from Cusabio (Cusabio Biotech, Wuhan, China).
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4

Measurement of Fasting Insulin and HOMA-IR

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For measurement of fasting blood insulin levels, mice were fasted overnight for 16 h and blood was collected from the caudal vein. Plasma insulin levels were detected by insulin ELISA kit (CUSABIO, Wuhan, China) according to kit instructions. The Homeostasis Model Assessment of IR (HOMA-IR) has proved to be a robust tool for the surrogate assessment of insulin resistance.28 (link) HOMA-IR can be calculated with the following formula: HOMA-IR index=fasting glucose (mmol/L)×fasting insulin (mU/L)/22.5.29 (link),30 (link)
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5

Metabolic Profiling of Mouse Model

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Food intake and body weight were measured once a week. Briefly, for the glucose tolerance test (GTT), mice which were fasted overnight were injected (i.p.) with D-glucose (1 g/kg body weight; Sigma-Aldrich) after 12 h fasting. For the insulin tolerance test (ITT), mice were injected (i.p.) with insulin (0.75 units/kg body weight; Novolin R, Novo Nordisk, Copenhagen, Denmark) after 6 h fasting. Glucose concentrations were measured in tail venous blood using an automated glucometer (Roche Diagnostics) up to 90 min or 120 min after injection.
Fasting insulin was measured by the insulin ELISA kit (Cusabio, Wuhan, China). Liver concentrations of triglyceride (TG) was measured by the triglyceride assay kit (Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Serum concentrations of total cholesterol (TC), triglyceride (TG), high density lipoprotein (HDL), low density lipoprotein (LDL), apolipoprotein E (ApoE), FFA and hsCRP were measured by enzymatic method using an automatic biochemical analyzer (Beckman AU5800, USA).
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6

Glucose Tolerance and Insulin Sensitivity Evaluation

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For the evaluation of glucose tolerance, all the rats were given glucose orally (2.0 g/kg BW) after overnight fasting prior that the animals were euthanized. Blood samples were collected from the tail vein at 0, 15, 30, 60, 90 and 120 min, and glucose was measured using a glucose metre (Roche, Germany). The serum was centrifuged at 4℃ (4000 rpm, 900 × g) for 15 min and stored at −80℃ for assay. Serum insulin level was determined by commercially available insulin ELISA kit (CUSABIO, Wuhan). The zero‐time value was taken as the fasting blood glucose value and fasting insulin value. The homeostatic model assessment of insulin resistance (HOMA‐IR) index was calculated according to the following formulas:
HOMA‐IR = (FBG × FINS)/22.5,
where FBG is the fasting blood glucose level and FINS is the fasting insulin level.
The insulin sensitivity index was calculated by the ratio of area under the glucose curve to area under the insulin curve (AUCg/AUCi).
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7

Enzyme-linked Immunoassay for Insulin Resistance

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FINS were measured by using an enzyme-linked immunosorbent assay insulin ELISA kit (CSB-E05070r, CUSABIO BIOTECH Co., Ltd, Wuhan, China). Homeostasis Model Assessment-Insulin Resistance (HOMA-IR) was applied to assess insulin resistance by the following formula: HOMA score = fasting serum insulin (μU/mL) × fasting glucose (mmol/L)/22.5 [13 (link), 14 (link)]. After logarithmic transformation the statistical analysis was performed.
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