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Quantichrom creatinine assay kit dict 500

Manufactured by BioAssay Systems
Sourced in United States

The QuantiChrom Creatinine Assay Kit (DICT-500) is a colorimetric assay kit designed to quantify creatinine levels in a variety of biological samples. The kit employs a simple, one-step protocol that allows for rapid and accurate measurement of creatinine concentration.

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14 protocols using quantichrom creatinine assay kit dict 500

1

Urine Albumin-to-Creatinine Ratio in Mice

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Twenty-four-hour urine was collected from mice using metabolic cages and urine albumin was determined using a commercial assay from Bethyl Laboratory Inc. (Houston, Texas, USA). Urine creatinine levels were measured in the same samples using the QuantiChrom Creatinine Assay Kit (DICT-500) (BioAssay Systems) according to the manufacturer's instructions. The urine albumin excretion rate was expressed as the ratio of albumin to creatinine.
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2

Urine Albumin and Creatinine Quantification

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Urine was collected weekly and albumin concentrations were analyzed as instructed using a mouse albumin ELISA kit #MSAKT from Molecular Innovations (Novi, MI). Albumin levels were normalized to creatinine using QuantiChrom Creatinine Assay Kit (DICT-500) (BioAssay Systems, Hayward, CA) according to the manufacturer's instructions.
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3

Measurement of Urinary Parameters in Water-Deprived Mice

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Mice were acclimated for few days in metabolic cages (3600M021; Techniplast, West Chester, PA, USA). Following acclimation and baseline measurements of urinary parameters, mice were water deprived for 24 hours, as we did previously [25 (link)]. Tails were clipped with sterilized scissors to collect 50 μl blood into heparinized micro-hematocrit capillary tubes (Fischer, Cat. # 22-362-566) before and after water deprivation. Urine and plasma osmolarity was measured in duplicates using freezing point depression osmometer Model 3320 (Advanced Instruments, Norwood, MA, USA). Urinary creatinine concentration was assessed with QuantiChrom Creatinine Assay Kit (DICT-500; BioAssay Systems, Hayward, CA, USA) utilizing the improved Jaffe method, as we did before [30 (link)]. Urinary AVP levels were assayed with Vasopressin Arg8-Vasopressin ELISA kit (Enzo Life Sciences, Farmingdale, NY, USA) following the manufacturer’s protocols. Urinary Ca2+ concentration was measured using a Jenway PFP7 Flame photometer (Bibby Scientific, Burlington, NJ, USA).
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4

Mouse Serum Creatinine Quantification

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Fresh mouse blood samples were centrifuged at 2500 rpm at 4° for 10 min. Serum creatinine levels were detected using the Quantichrom Creatinine Assay Kit (DICT‐500; BioAssay Systems) as the manufactural instructions.
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5

Colorimetric Assays for Creatinine and Urea

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Creatinine levels were measured in serum by a quantitative colorimetric method using a QuantiChrom Creatinine Assay Kit (DICT-500), supplied by BioAssay Systems, Hayward, CA, USA, following the manufacturer’s instructions and according to the modified Jaffe method [18 (link)].Urea levels were measured in serum by a quantitative colorimetric method according to [20 (link)] using a QuantiChrom Urea Assay Kit (DIUR-500), supplied by BioAssay Systems, Hayward, CA, USA, according to the manufacturer’s instructions.
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6

Quantifying Urinary Albumin in Mice

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Timed (12-hour) urine collections were obtained from mice using metabolic cages. Urine protein was measured by an ELISA kit (Bethyl Laboratory, Houston, TX) for albumin, and urine creatinine levels were quantified using a QuantiChrom Creatinine Assay Kit (DICT-500; Bioassay Systems). Urine albumin excretion was expressed as the UACR. As for the reproducibility of this assay, the coefficients of variance (CV) was less than 3% when the same sample was measured three times consecutively.
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7

Urine Albumin and BUN Quantification

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Urine Albumin measurements were determined by using Molecular Innovation’s (Novi, MI) Mouse Albumin Antigen Assay (cat. # MSAKT) and normalized using BioAssay Systems (Hayward, CA) QuantiChrom Creatinine Assay Kit (DICT-500). BUN measures were performed using a Cobas Integra 400 plus analyzer (Roche) in accordance with the manufacturer’s instructions.
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8

Measuring Oxytocin in Infant Plasma and Urine

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We measured plasma and urinary OT using an extraction-free, commercially available kit (KIT S-1355.0001; Peninsula Laboratories International, Inc., San Carlos, CA). Samples were not extracted due to safety and ethical concerns of taking larger amounts of body fluids from medically fragile infants. Samples were immediately placed on ice, transported to the laboratory, and then centrifuged at 4°C and 2,000 g for 10 min within 1 hr of collection. Supernatants were collected and stored at −80°C until analysis. We assayed samples in batches to minimize the time they spent in storage. To avoid interassay variation, we assayed samples from the same infant simultaneously, and we performed all measurements in duplicate. Intraassay coefficient of variation for the study was 12%. We measured creatinine concentrations using a commercially available kit (QuantiChrom Creatinine Assay Kit: DICT-500; Bioassay Systems, Hayward, CA) and normalized urinary OT levels to total creatinine. We did not normalize blood for protein content, as we had measured a portion of samples for protein and found that levels changed minimally and would not affect analysis. We analyzed data using GraphPad Prism software (version 6).
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9

Urinary C2C Neoepitope Quantification

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The study subjects were instructed to collect urine from the second morning void. Urine samples were stored at −80 °C on the day of collection. Urinary levels of collagenase-generated C2C neoepitope fragments of human Col2 were measured by the IBEX C2C human urine sandwich assay (IB–C2C-HUSA) in IBEX Pharmaceuticals (IBEX Pharmaceuticals Inc., Montreal, Quebec, Canada). The assay details and performance characteristics have been described by Poole et al. [6 (link)] and https://www.ibex.ca/product-catalog/. All samples were tested in duplicate, and each measured C2C concentration was corrected with the creatinine concentration in the same urine sample, determined by using the QuantiChrom™ Creatinine Assay kit (DICT-500; BioAssay Systems, Hayward, USA).
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10

Urinary Biomarkers in Cardiac Bypass

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Urine samples were collected 2.5–4 h after the end of cardiac bypass and immediately frozen (−20°C) before subsampling and refrozen for long-term conservation (−80°C). Urinary peptidome analysis was performed as previously described [8 (link)]. For urinary neutrophil gelatinase-associated lipocalin (uNGAL) measurement, urine samples were centrifuged for 10 min at 2500 rpm. NGAL was measured using an enzyme-linked immunosorbent assay (Human Lipocalin-2/NGAL Duoset ELISA; DY1757; R&D Systems, Minneapolis, MN, USA) in diluted supernatant (1:10 or 1:100) according to the manufacturer's protocol. Creatinine was measured using the QuantiChrom Creatinine Assay Kit (DICT 500; BioAssay Systems, Hayward, CA, USA) according to the manufacturer's protocol. Creatinine-normalized uNGAL (μg/g) was used for performance evaluations. [TIMP-2] and [IGFBP7] were measured in urine supernatants using the VITROS NephroCheck immunoassay on a VITROS 5600 Integrated System (Ortho Clinical Diagnostics, Raritan, NJ, USA) according to the manufacturer's instructions. The VITROS NephroCheck test result is a single number, which is a product of the measured concentrations of the two analytes in the sample divided by 1000. Certified laboratory technicians blinded to clinical data performed the analyses.
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