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S acp

Manufactured by Solarbio
Sourced in China

S-ACP is a laboratory equipment designed for the measurement of acyl-CoA concentration. It utilizes a colorimetric assay method to quantify the presence of acyl-CoA, a key metabolite involved in various cellular processes.

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3 protocols using s acp

1

Soil Enzyme Activity Quantification

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The rhizosphere soil activities of acid phosphatase (S-ACP, BC0285), nitrate reductase (S-NR, BC3105), and sucrase (S-SC, BC0245) were quantified using the corresponding kits obtained from the Solarbio Corporation, China. Additionally, kits for measuring the activity of soil urease (S-UE, SUE-2-Y), catalase (S-CAT, SCAT-2-Y), neutral protease (S-NPT, SNPT-1-Y), amylase (SA, SDM-2-G), neutral phosphatase (S-NP, SNP-2-W), and dehydrogenase (SDHA, SDHA-2-G) were obtained from the Suzhou Kemin Biotechnology Co., Ltd., China.
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2

Soil Enzyme Activity Assay

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Five soil samples from treated and untreated sites were analyzed for three representative enzymes activities (soil urease (S-UE), soil acid phosphatase (S-ACP) and soil β-glucosidase (S-β-GC). Soil enzyme activities were analysed with the S-UE, S-ACP, and S-β-GC assay kit (Solarbio life Sciences, Beijing, China). S-UE was defined as 1 g of soil which produced 1 μg NH3-N (U/g) daily. S-ACP was considered to be 1 g of soil which liberated 1 nmol phenol at 37℃ (U/g) daily. S-β-GC was considered to be 1 g of soil which produced 1 μmol p-nitroohenol (U/g) daily (Dick et al. 2013 (link)). All enzyme assays were conducted in duplicate.
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3

Soil Enzyme Activity Assay

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Five soil samples from treated and untreated sites were analyzed for three representative enzymes activities (Soil Urease (S-UE), Soil acid phosphatase (S-ACP) and Soil β-glucosidase (S-β-GC). Soil enzyme activities were analysed with the S-UE, S-ACP, and S-β-GC assay kit (Solarbio life Sciences, Beijing, China). S-UE was de ned as 1 g of soil which produced 1µg NH 3 -N (U/g) daily. S-ACP was considered to be 1 g of soil which liberated 1nmol phenol at 37℃ (U/g) daily. S-β-GC was considered to be 1 g of soil which produced 1µmol p-nitroohenol (U/g) daily (Dick et al. 2013) (link). All enzyme assays were conducted in duplicate.
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