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Ezradp 62k

Manufactured by Merck Group
Sourced in United States

The EZRADP-62K is a laboratory equipment product from Merck Group. It is a multi-channel pipette that can accurately and precisely dispense liquids across a range of volumes. The core function of the EZRADP-62K is to facilitate liquid handling tasks in various laboratory settings.

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5 protocols using ezradp 62k

1

Quantitative Biomarker Measurements in Serum

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Quantitative estimations of leptin (cat. EZRL-83K; Millipore, St. Charles, MO, USA), adiponectin (cat. EZRADP-62K, Millipore, MO, USA), C-reactive protein (cat. CYT294; Millipore, St. Charles, MO, USA) and PAI-1 serum levels (cat. Ab198509, Abcam, Cambrige, UK) were performed following the manufacture’s protocols using specific ELISA kits.
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2

Plasma Biomarker Measurement Protocol

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Plasma adiponectin, insulin, and leptin concentrations were determined using specific enzyme-linked immunosorbent assay kits (EZRADP-62K, EZRMI-13K, and EZRL-83K, respectively) from Millipore (Billerica, MA, USA). Insulin growth factor 1 (IGF1) determination was carried out using enzymatic kit (ab213902, Abcam, Cambridge, UK). Non-esterified fatty acid (NEFA) colorimetric kit was obtained from BiooScientific (Austin, TX, USA) and Uric acid kit from SpinReact (Girona, Spain) (Ref. no. 1001010). Plasma samples were assayed in duplicate.
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3

Western Blot Analysis of Adiponectin Receptors

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Protein lysates were subjected to separation using sodium dodecyl sulfate-polyacrylamidegel electrophoresis, transferred to polyvinylidene fluoride membranes and blocked in 5% non-fat dry milk for 2 hours at room temperature as described, previously 30 (link), 31 (link). Membranes were probed overnight at 4°C with primary antibodies at a dilution of 1:1000 for AdipoR1 (42 kDa, AdipoR1-2; Alpha Diagnostics), 1:2000 for AdipoR2 (42 kDa, AdipoR2-1; Alpha Diagnostics), 1:500 for phosphorylated AMPK (phospho-AMPK, Thr-172; 62kDa; 2535; Cell Signaling), and 1:1000 for AMPK (63 kDa, 07-350; Millipore). Membranes were then incubated with HRP-linked anti-rabbit secondary antibody at a dilution of 1:20,000 for 1 h at 28°C and visualized using ECL (GE Healthcare). Densitometry was performed using Scion Image (NIH). To correct for potential protein loading errors all membranes were stained with Sypro Ruby blot stain (Invitrogen) and densitometry was performed as previously described 30 (link), 31 (link).Rat serum was assessed for total APN concentration utilizing a kit (EZRADP-62K; Millipore) per manufacturer instructions.
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4

Metabolic Biomarkers in Blood Assessment

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Serum adiponectin, insulin, and leptin concentrations were determined using specific ELISA kits (EZRADP-62K; EZRMI-13K; and mEZRL-83K, respectively) from Millipore (Billerica, MA, USA). The non-esterified free fatty acids (NEFA) colorimetric kit was from Bioo Scientific (Austin, TX, USA), and the kits for alanine (ALT) and aspartate aminotransferase (AST) kinetics were from SpinReact (Girona, Spain). The insulin sensitivity index (ISI) was calculated as 2/[insulin (nM) × blood glucose (µM) + 1].
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5

Adiponectin, Insulin, and Leptin Biomarkers

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Serum adiponectin, insulin, and leptin concentrations were determined using specific ELISA kits (EZRADP‐62K; EZRMI‐13K; EZRL‐83K, respectively) from Millipore (Billerica, MA, USA). The non‐esterified free fatty acids (NEFA) colorimetric kit was from BiooScientific (Austin, TX, USA) and the kits for alanine (ALT) and aspartate aminotransferase (AST) kinetics were from SpinReact (Girona, Spain). The insulin sensitivity index (ISI) was calculated as 2/ [insulin (nM) X blood glucose (µM) + 1].[44]
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