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Blood ammonia assay kit

Manufactured by Nanjing Jiancheng
Sourced in China

The Blood Ammonia Assay Kit is a laboratory tool designed to quantitatively measure the concentration of ammonia in blood samples. It provides a standardized method for the analysis of this important biochemical marker.

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3 protocols using blood ammonia assay kit

1

Serum Ammonia Quantification Protocol

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The serum ammonia content was determined using a blood ammonia assay kit according to the manufacturer's instruction (Nanjing Jiancheng Bioengineering Institute, China).
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2

Hemolymph Ammonia Quantification

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The ammonia concentration in hemolymph was determined according to the instructions of the blood ammonia assay kit (No. A086-1-1, Nanjing Jiancheng Bioengineering Institute, Nanjing, China). Hemocyanin was precipitated with protein precipitant to block enzyme activity, prevent the production of free ammonia, and remove most of the substances that interfered with color. Ammonia was prepared in protein-free filtrate by the Berthelot reaction. In this non-enzymatic ammonia assay protocol, ammonia is used to form indophenol, a highly colored product easily quantifiable by colorimetry (λ = 630 nm) using a plate reader. Then, the ammonia concentration in hemolymph was calculated by comparison to the standard solution.
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3

Multimodal Monitoring in ALF Induction

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After ALF induction, all monkeys were monitored every 12 h for the first 48 h and every 24 h for the remainder of the study. During the 6 h treatment, animals were monitored every hour (Figure 1B). Vital signs were recorded by cardiogram monitoring. Blood samples were collected for subsequent analyses. Serum biochemistry was assayed using a chemistry analyzer AU5800 series (Beckman Coulter). Ammonia concentrations were quantified by a blood ammonia assay kit (Nanjing Jiancheng, Nanjing, China). S-100 β proteins have emerged as a biomarker of blood-brain barrier (BBB) permeability and neuropathological conditions including encephaledema and increased ICP 13 (link), 14 (link). Thus, elevated S-100 β levels were measured using an ELISA kit (Ruikesi, Chengdu, China). Rhesus IgG and IgM levels were detected using ELISA kits (Ruikesi). All the kits were analyzed with a MQX 200 microplate reader (BioTek Instruments Inc., VT, US). Cytokines were assessed using a Luminex 100 instrument with xPONENT 3.1 software using Monkey Cytokine Magnetic 29-Plex Panel (Invitrogen, CA, US).
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