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E el 0047c

Manufactured by Elabscience
Sourced in China

E-EL-0047c is a laboratory instrument designed for the measurement of pH values. It features a digital display and allows for the precise determination of pH levels in various samples.

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7 protocols using e el 0047c

1

Measuring 5-HT and NE in Depression

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Blood samples were collected both at RW and after SD, which were performed after the HAMD assessment and MRI scan. Because the procedure of blood sample collection was invasive, only 17 paired samples were finally obtained. Blood was collected into ethylenediaminetetraacetic acid tubes (5 ml, for measurement of 5-HT and NE). Samples were left standing at room temperature for at least 30 min. The supernatant serum was removed after centrifuging at 3,000 × g for 10 min in a 4°C centrifuge. Then, a 600-μl liquid component was immediately transferred in Eppendorf tubes, which were stored at a −80°C refrigerator until further use. Enzyme-linked immunosorbent assay was performed to measure the concentrations of 5-HT (Elabscience, E-EL-0033c, China) and NE (Elabscience, E-EL-0047c, China) following the manufacturer's instruction (27 (link)).
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2

Measuring Serum Insulin and Norepinephrine

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The serum insulin and norepinephrine concentrations of rats were measured by using ELISA kits (E-EL-R2466c and E-EL-0047c, respectively; Elabscience, China).
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3

Quantifying NE and VMA Levels

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The levels of NE and VMA were determined by Human ELISA kits following manufacturer’s instructions (Elabscience, E-EL-0047c; Elabscience, E-EL-0132c). For tissue samples, collected tumor tissues and pairing para-tumor tissues from early-stage ovarian cancer patients were homogenized in ice-cold 0.01M hydrochloric acid before measurement. For cell samples, 5 × 106 cells were harvested, washed with PBS, and lysed in 500 μL RIPA Lysis buffer (Pierce, 89900) on ice for 20 min. Then the samples were centrifuged at 1000 ×g at 4°C for 15 min, and the supernatant was used for the measurement of NE and VMA. For uterine fluid samples, measurements were conducted following the standard protocols without additional pretreatment.
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4

ELISA Analysis of Plasma NE and 3-NT

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ELISA analysis was conducted according to the manufacturer’s instructions. The plasmic NE concentration in the rats was measured by using NE ELISA kit (E-EL-0047c, Elabscience). 3-NT concentration in the supernatant of culture medium of microglia was measured using Nitrotyrosine ELISA kit (ab113848, Abcam).
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5

Measuring sFRP1 Levels in NE-Treated Cells

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The sFRP1 level in conditioned media collected from cells treated with NE was measured by an ELISA kit (R&D Systems, Wiesbaden, Germany) following the manufacturer’s instructions. For NE, tissue was homogenized in 0.01 M HCl at 10% volume (ml) by tissue weight. NE in serum and tissue was quantified by ELISA (Elabscience, E-EL-0047c, China) according to the manufacturer’s protocol, as described previously [28 (link)].
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6

Quantifying neurotransmitters in PC12 cells

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The levels of norepinephrine (NE) and methionine enkephalin (M-EK) in the PC12 cell supernatant and mouse spinal cord homogenate were detected using ELISA methods, and the operation was performed according to the instructions of the ELISA kit (cat. nos. E-EL-0047c and E-EL-0020c; Elabscience Biotechnology Co., Ltd.). The absorbance was measured at 450 nm using an enzyme-labelled meter (Multiskan Mk3; Thermo Fisher Scientific, Inc.). Each sample was repeated in triplicate.
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7

ELISA-Based Biomarker Quantification in Rat Serum

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ELISA kit was applied to detect the contents of norepinephrine (NE) (E-EL-0047c, Elabscience, Wuhan, China, https://www.elabscience.cn), alanine aminotransfease (ALT) (E-EL-R1232km-1, Elabscience) and aspartate aminotransferase (AST) (E-EL-R0076c, Elabscience) in rat serum. The kit was taken out to stand for 30 min at room temperature. The standard group (6 concentrations), the blank group and the sample group to be tested were set. The samples were added as follows: 100 μL of the standard solution was added to the blank well in the standard group; 100 μL distilled water was added to the blank well. The remaining wells were filled with 100 μL of samples to be tested. 50 μL hydrocresol peroxide solution was added to each well of the standard group and the sample group to be tested. Then, the label board was sealed with sealing paper and incubated at 37°C for 1 hr. At the end of incubation, each well was filled with diluted detergent solution and stood for 15-30 sec. In addition, the label board was fully cleaned for 5 times and the paper was patted dry. 50 μL chromogenic solution A and 50 μL chromogenic solution B were added to each well, and reacted at 25-37°C in the dark for 15 min. Ultimately, 50 μL of termination fluid was added to terminate the reaction. OD value of each well at a wavelength of 450 nm was measured by Molecular Devices (Shanghai, China).
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