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Human glycated albumin elisa kit

Manufactured by Cusabio
Sourced in China

The Human glycated albumin ELISA kit is a laboratory equipment designed to quantitatively detect and measure glycated albumin levels in human samples. It utilizes the enzyme-linked immunosorbent assay (ELISA) technique to provide accurate and reliable results.

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2 protocols using human glycated albumin elisa kit

1

Glycated Protein Biomarkers in Diabetes

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Clinical and
biochemical parameters such as age, sex, FBG, HbA1c, blood
urea, serum creatinine, cholesterol, triglyceride, high-density lipoprotein
(HDL), fasting insulin, and CRP were measured for each participating
subject at Bharati Vidyapeeth (DTU) Medical College, Pune. Besides
these parameters, the plasma concentration of total protein (estimated
by Bradford’s method), fructosamine (using the fructosamine
assay kit from Abbexa Ltd, Cambridge, UK), albumin (using bromocresol
green albumin assay kit MAK124 from Sigma-Aldrich), glycated albumin
(using the Human glycated albumin ELISA kit, CSB-E09599h, Cusabio,
China), and MDA (using lipid peroxidation assay kit from Sigma-Aldrich),
were determined. The plasma fructosamine concentration was normalized
to total plasma protein concentration and was expressed as μM/g
of plasma protein. To determine the plasma glycated albumin concentration,
a four-parameter logistic regression curve was plotted using the web
tool GainData ELISA data calculator (Arigo Biolaboratories, Hsinchu
City 300, Taiwan). Glycated albumin concentration was normalized with
respective plasma albumin concentrations and expressed in μM/g
of albumin. HOMA-IR was calculated based on the following formula.23 (link)
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2

Determining Glycated Albumin Levels

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GA concentration was determined according to manufacturers' instructions using a competitive ELISA kit (Human glycated albumin ELISA Kit, CSB-E09599h, Cusabio, Wuhan, Hubei Province, China) [14 (link)]. Samples were diluted to 1:250 with the sample diluent buffer provided with the kit to achieve sample absorbance within the range of a standard curve. The absorbance was measured at 450 nm using a Synergy H1 hybrid multi-mode microplate reader (Biotek, Winooski, VT, USA). The amount of GA was determined by comparing with the known standard provided with the kit and expressed as nM/ml of GA present in human serum samples.
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