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Rat elisa kit

Manufactured by Boster Bio
Sourced in United States

The Rat ELISA kit is a laboratory tool designed to detect and quantify the presence of specific target analytes in rat samples. It utilizes the enzyme-linked immunosorbent assay (ELISA) principle to provide accurate and reliable results. The kit contains the necessary reagents and components required to perform the ELISA analysis.

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6 protocols using rat elisa kit

1

Oxidative Stress and Renal Function Evaluation

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On the 8th day, blood samples were collected for the estimation of oxidative stress parameters such as nitric oxide (NOx), malondialdehyde (MDA), total oxidative stress (TOS), and antioxidant parameters such as catalase (CAT) and total antioxidant capacity (TAC). Matrix metalloproteinases (MMP-2 and MMP-9), renal function (creatinine, blood urea nitrogen (BUN), and urea) were also assessed. At the end of the experiment, all the animals were euthanized after general anesthesia (ketamine—5 mg/kg body weight, i.p. route) [47 (link)] by cervical dislocation, after the blood sample collection from retro-orbital plexus.
A Jasco V-350 UV-VIS spectrophotometer (Jasco International Co, Ltd., Tokyo, Japan) was used for all measurements. The oxidative stress intensity (NOx, MDA, and TOS) and antioxidant capacity of plasma (CAT and TAC) parameters were measured by the methods described somewhere else [48 (link)]. Metalloproteinases assessment was made with a Stat Fax 303 ELISA reader (Quantikine, McKinley Place NE, MN, USA), using a rat ELISA kit (Boster Biological Technology, Pleasanton, CA, USA). Renal function parameters assessment was made by colorimetric methods [49 (link),50 (link)], and the reagents were purchased from Spinreact (Girona, Spain).
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2

Serum Biomarkers of Bone Turnover

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Serum samples were collected at the sacrifice time and stored at -80°C.
IL-6 is one of the most powerful proinflammatory cytokines and is a key signal for bone destruction. IL-6 was quantified in serum samples using a specific rat ELISA kit (Boster Bio, California, USA). Bone resorption marker CTX I reflects osteoclastic activity as it is a degradation product of type I collagen, the major structural protein of bone. The bone formation marker P1NP is a bio product of type I collagen synthesis and thus is a marker for osteoblastic activity. Bone remodeling markers, CTX-I and P1NP, were quantified by Serum Rat Laps ELISA assay (Immunodiagnostic Systems Ltd, Boldon, UK) in order to study the effects of inflammation on bone turnover.
For all biomarkers standard curves were generated by using reference biomarker concentrations supplied by the manufacturers. Samples were analyzed using a plate reader Infinite M200 (Tecan, Mannedorf, Switzerland).
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3

Oxidative Stress and Antioxidant Assessment

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Parameters associated with oxidative stress and antioxidant status were determined from collected blood samples. The parameters used to assess oxidative stress were: malondialdehyde (MDA) [47 (link)], indirect nitric oxide (NOx) synthesis assessment [48 ], and total oxidative status (TOS) [49 (link)]. Antioxidant status parameters were represented by total antioxidant capacity of plasma (TAC) [50 (link)], thiols [51 (link)], and catalase [52 (link)]. All measurements were performed using a Jasco V-350 UV-VIS spectrophotometer (Jasco International Co, Ltd., Tokyo, Japan). Matrix metalloproteinases (MMPs) were appraised from serum using a rat ELISA kit (Boster Biological technology, Pleasanton, CA, USA) and a Stat Fax 303 ELISA reader (Quantikine, McKinley Place NE, MN, USA).
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4

Cytokine and Iron Regulation in Placenta

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Cytokine concentrations of IL-6, IL-1β, and TNF-α in placental tissues and plasma with or without L-NAME treatment were detected by ELISA kits (Jiancheng, Nanjing, China). The levels of ferritin (FER) and transferrin (TF) were measured with rat ELISA kits (Boster, Wuhan, China) as per the manufacturer’s instructions.
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5

Cytokine and AQP1 Quantification

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The concentrations of four cytokines, tumour necrosis factor alpha (TNF-α), interleukin 6 (IL-6), iNOS, and Arg-1, and the concentration of AQP1 in plasma and kidney homogenates were detected with rat ELISA kits (Boster, Wuhan, China). The cytokine concentrations in cell supernatants were quantified using mouse ELISA kits. The procedures were performed according to the manufacturers’ instructions.
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6

Liver TNF-α and IL-6 Quantification

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We used rat ELISA kits from Boster Biological Technology, specifically the Picokine™ kits, USA, to quantitatively assess TNF-α in the liver homogenate. For IL-6, we used kits from the Norcross, GA, USA producer. All measurements were taken following the guidelines provided by the producer.
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