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Rat OxLDL(Oxidized Low Density Lipoprotein) ELISA Kit

Cat.No.:E-EL-R0710
Reactivity: Rat

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Product Details

Properties

Assay type	Sandwich-ELISA
Format	96T/48T
Assay time	3.5h
Detection range	0.47-30 ng/mL
Sensitivity	0.28 ng/mL
Sample type &Sample volume	serum, plasma and other biological fluids; 100μL
Specificity	This kit recognizes Rat OxLDL in samples. No significant cross-reactivity or interference between Rat OxLDL and analogues was observed.
Reproducibility	Both intra-CV and inter-CV are < 10%.
Application	This ELISA kit applies to the in vitro quantitative determination of Rat OxLDL concentrations in serum, plasma and other biological fluids.

Test Principle

This ELISA kit uses the Sandwich-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with an antibody specific to Rat OxLDL. Standards or samples are added to the micro ELISA plate wells and combined with the specific antibody. Then a biotinylated detection antibody specific for Rat OxLDL and Avidin-Horseradish Peroxidase (HRP) conjugate are added successively to each micro plate well and incubated. Free components are washed away. The substrate solution is added to each well. Only those wells that contain Rat OxLDL, biotinylated detection antibody and Avidin-HRP conjugate will appear blue in color. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The OD value is proportional to the concentration of Rat OxLDL. You can calculate the concentration of Rat OxLDL in the samples by comparing the OD of the samples to the standard curve.

Kit components & Storage

An unopened kit can be stored at 2-8℃ for 1 month. If the kit is not supposed to be used within 1 month, store the components separately according to the following conditions once the kit is received.

Item	Specifications	Storage
Micro ELISA Plate(Dismountable)	96T: 8 wells ×12 strips 48T: 8 wells ×6 strips	-20℃, 6 months
Reference Standard	96T: 2 vials 48T: 1 vial
Concentrated Biotinylated Detection Ab (100×)	96T: 1 vial, 120 μL 48T: 1 vial, 60 μL
Concentrated HRP Conjugate (100×)	96T: 1 vial, 120 μL 48T: 1 vial, 60 μL	-20℃(Protect from light), 6 months
Reference Standard & Sample Diluent	1 vial, 20 mL	2-8°C, 6 months
Biotinylated Detection Ab Diluent	1 vial, 14 mL
HRP Conjugate Diluent	1 vial, 14 mL
Concentrated Wash Buffer (25×)	1 vial, 30 mL
Substrate Reagent	1 vial, 10 mL	2-8℃(Protect from light)
Stop Solution	1 vial, 10 mL	2-8°C
Plate Sealer	5 pieces
Manual	1 copy
Certificate of Analysis	1 copy

Technical Data

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Rat OxLDL were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Rat OxLDL were tested on 3 different plates, 20 replicates in each plate.

	Intra-assay Precision			Inter-assay Precision
Sample	1	2	3	1	2	3
n	20	20	20	20	20	20
Mean (ng/mL)	1.60	2.60	12.20	1.50	2.50	13.00
Standard deviation	0.10	0.10	0.50	0.10	0.10	0.40
CV (%)	6.25	3.85	4.10	6.67	4.00	3.08

Recovery

The recovery of Rat OxLDL spiked at three different levels in samples throughout the range of the assay was evaluated in various matrices.

Sample Type	Range (%)	Average Recovery (%)
Serum(n=8)	95-107	102
EDTA plasma (n=8)	89-104	96
Cell culture media (n=8)	91-103	97

Linearity

Samples were spiked with high concentrations of Rat OxLDL and diluted with Reference Standard & Sample Diluent to produce samples with values within the range of the assay.

Target Information

Synonyms	OL
Research Area	Cancer, Cardiovascular, Metabolism, Signal transduction

Assay Procedures

	1. Add 100μL standard or sample to the wells. Incubate for 90 min at 37°C
	2. Discard the liquid, immediately add 100μL Biotinylated Detection Ab working solution to each well. Incubate for 60 min at 37°C
	3. Aspirate and wash the plate for 3 times
	4. Add 100μL HRP conjugate working solution. Incubate for 30 min at 37°C. Aspirate and wash the plate for 5 times
	5. Add 90μL Substrate Reagent. Incubate for 15 min at 37°C
	6. Add 50μL Stop Solution
	7. Read the plate at 450nm immediately. Calculation of the results

Citations

From now on, if you have published a paper by using any of our products since 1/1/2019, fill out the “Elabscience Publication Reward Application Form”carefully and send it to orders@elabscience.com, we will get back to you with the reward after we confirm it ASAP!

View more details about our Publication Reward >>

Oxidative medicine and cellular longevity (2019) IF: 5.076

Tissue-Specific Oxidative Stress Modulation by Exercise: A Comparison between MICT and HIIT in an Obese Rat Model

DOI: 10.1155/2019/1965364
PMID: 31396298	Sample: Plasma,Tissue homogenate

Oxidative Medicine and Cellular Longevity (2016) IF: 4.593

Aai (Euterpe Oleraceamart.) Upregulates Paraoxonase 1 Gene Expression And Activity With Concomitant Reduction Of Hepatic Steatosis In High-Fat Diet-Fed Rats.

DOI: 10.1155/2016/8379105
PMID: 27642496	Sample: Serum

Food & Nutrition Research (2015) IF: 2.039

N-Acetylneuraminic Acid Attenuates Hypercoagulation On High Fat Diet-Induced Hyperlipidemic Rats.

DOI: 10.3402/fnr.v59.29046
PMID: 26642300	Sample: Serum

Food & Nutrition Research (2015) IF: 2.039

N-Acetylneuraminic Acid Attenuates Hypercoagulation On High Fat Diet-Induced Hyperlipidemic Rats.

DOI: 10.3402/fnr.v59.29046
PMID: 26642300	Sample: Serum

Drug Design (2015) IF: 2.822

Edible Bird’S Nest Attenuates Procoagulation Effects Of High-Fat Diet In Rats.

DOI: 10.2147/DDDT.S87772
PMID: 26251574	Sample: Serum

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