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Cystatin c elisa kit

Manufactured by R&D Systems
Sourced in United States, Czechia

The Cystatin C Elisa kit is a quantitative sandwich enzyme-linked immunosorbent assay (ELISA) designed for the measurement of Cystatin C levels in biological samples such as serum, plasma, urine, and cell culture supernatants.

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4 protocols using cystatin c elisa kit

1

Plasma Biomarker Measurement in Mice

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Blood samples were collected with a heparinized syringe before mice were sacrificed. Plasma creatinine level was determined using a Detect X Serum Creatinine Detection Kit (Arbor Assays, Ann Arbor, MI, USA. Cystatin C level was measured using a cystatin C Elisa kit (R&D systems, Minneapolis, MN, USA). Plasma LPO level was measured by reacting with thiobarbituric acid as described previously [34 (link)].
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2

Biomarkers in Cirrhosis Progression

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In the groups without ascites and with ascites but without treatment, serum samples were collected when patients presented at the hospital. In the group with ascites and treatment, serum collection was performed immediately before the administration of tolvaptan. Albumin (g/dL), total bilirubin (mg/dL), sodium (mEq/L), creatinine (mg/dL), BUN (mg/dL), CRP (mg/dL), α-fetoprotein (AFP; ng/mL) and des-γ-carboxy prothrombin (DCP; mAU/mL) were measured. Serum samples were kept at -80 °C until copeptin (pmol/L), ZAG (μg/dL), cystatin C (mg/dL), NGAL (ng/mL) and L-FABP (ng/mL) measurements were performed using an automated copeptin immunofluorescent assay kit (Thermo Fisher Scientific Inc., Tokyo, Japan), ZAG enzyme-linked immunosorbent assay (ELISA) kit (BioVendor, Brno, Czech Republic), cystatin C ELISA kit (R&D Systems, Minneapolis, MN, USA), NGAL ELISA kit (R&D Systems) and high-sensitivity human L-FABP ELISA kit (CMIC Holdings, Tokyo, Japan), respectively.
The Child-Pugh score, albumin-bilirubin (ALBI) score (18 (link)), fibrosis index based on 4 factors (FIB-4) (19 (link)), model for end-stage liver disease (MELD) score, MELD-Na score and estimated glomerular filtration rate (eGFR) with Cockcroft and Modification of Diet in Renal Disease (MDRD) formula were calculated.
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3

Ethanol-Induced Kidney Injury in Wistar Rats

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Adult male Wistar rats (~170–180 g) were purchased from Harlan Sprague-Dawley, Inc. (Indianapolis, IN). Lieber-deCarli liquid ethanol diet was from Dyets (Bethlehem, PA) and taurine from Sigma (St. Louis, MO). Anti-albumin antibody was from Santa Cruz Biotechnology (Santa Cruz, CA), anti-4-hydroxynonenal antibody from Alpha Diagnostics (San Antonio, TX), while anti-myeloperoxidase, and anti-neutrophil gelatinase associated lipocalin (NGAL) antibodies were from Abcam (Cambridge, MA). Kits for blood urea nitrogen (BUN), and creatinine were purchased from Arbor Assays (Ann Arbor, MI). Anti-KIM-1 antibody, TUNEL assay kits, KIM-1 ELISA kits and cystatin C ELISA kits were from R&D Systems (Minneapolis, MN). Caspase-3 Apo-ONE Homogeneous caspase-3/7 fluorescence assay kits were the product of Promega (Madison, WI) and myeloperoxidase activity assay kits were from Cell Technology (Mountain View, CA).
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4

Quantification of Renal Biomarkers

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BUN, and serum and urinary creatinine were quantified by kits according to the manufacturer’s (Arbor Assays) protocol. Quantichrom BCG Albumin Assay Kits (BioAssay Systems) were used to measure serum and urinary albumin. KIM-1 and cystatin c ELISA kits (R&D Systems) were used to measure urinary proteins.
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