UCH-L1 IMR Reagent

“MagQu” UCH-L1 IMR Reagent is designed for quantitative measurement of Tau protein concentration in human plasma by immunomagnetic reduction (IMR) assay. The reagent can be used with MagQu’s Magnetic Immunoassay Analyzer XacPro-S system.
This assay enables early-stage neurological disease research with ultra-high sensitivity and low interference.

Features

  • Quantifying UCH-L1 in the sample easily, rapidly, and accurately

  • Magnetic Nanoparticle

  • Dextran layer

  • For traumatic brain injury and Alzheimer’s disease research and for in-vitro diagnosis use

Specifications

Sample type: Human Plasma

Sample volume: 60 μl

Assay time: 5 hours (36 channels in XacPro-S)

Use application: In vitro diagnostic

Detection methods: ImmunoMagnetic Reduction (by analyzer XacPro-S with magnetic reagents)

Sensitivity

Detection Range: 1 - 100 pg/ml

Low detection limit: 3.3 fg/ml

IMR standard curve of UCH-L1

Description

Intended Use

“MagQu” UCH-L1 IMR Reagent is used to quantitatively measure ubiquitin C-terminal hydrolase L1(UCH-L1) in human fluid specimen, such as plasma, serum or CSF.
Use “MagQu” UCH-L1 IMR Reagent only with the XacPro-S System (MagQu Co., Ltd.).

Introduction

Ubiquitin C-terminal hydrolase L1 (UCH-L1) is an extremely abundant deubiquitinating enzyme in brain, which involved in the elimination of misfolded proteins. UCH-L1 is not essential for neuronal development, but is necessary for maintenance of integrity. Recent studies have found an association between UCH-L1 dysfunction and neurodegenerative diseases. In previous studies, UCH-L1 expression was found to be decreased in patients with ischemic injury and Alzheimer's disease. It is possible that UCH-L1 increases free ubiquitin expression by promoting ubiquitination and accelerates lysosomal degradation of amyloid β-synuclein or α-synuclein, which tend to accumulate when they are reduced. Over-expression of UCH-L1 has also been shown in mouse models to effectively delay the progression of Alzheimer's disease. Thus, UCH-L1 may be a pre-dementia process with the potential to predict the onset of dementia. 1,2,3

Principles of Test

“MagQu” UCH-L1 IMR Reagent is designed for rapid quantifying UCH-L1 by ImmunoMagnetic Reduction (IMR). We conjugate antibody on the surface of around 50 nm-in-diameter Fe3O4 magnetic particles. When the antibodies on the surface bind with UCH-L1, the magnetic particles form clusters. Therefore, the ac susceptibility (Xac) of magnetic particles would be reduced in the adding ac magnetic field. By measuring the reduction of Xac, UCH-L1 can be easily, rapidly and accurately quantified.4

Reagent Properties

Property Detail
Core Iron Oxide (Fe3O4)
Layer Dextran
Surface protein Anti-UCH-L1 antibody
Mean Diameter of Particles 50 ~ 60 nm
The analytical range of reagent 1 to 100 pg/mL UCH-L1 protein
Buffer pH 7.4 PBS
Storage temp. 2 ~ 8℃

Precision

PRECISION

The UCH-L1 samples were measured in duplicate,

twice per day over 20 days. Two different UCH-L1

concentrations were used for the tests. The

standard deviations of repeatability and within-lab

for various UCH-L1 concentrations ware obtained.

Interference (Specificity)

Plasma can contain interfering substances such

as hemoglobin, bilirubin, or intra lipid because of

common diseases, such as hemolysis, jaundice

or hypertriglyceridemia. Other bio-substances

that exist naturally in plasma, such as uric acid,

rheumatoid factor, or albumin, are also interfer-

ing substances.

Other interfering substances include drugs or

chemicals in medicine that is used to treat

inflammatory diseases, viral and bacterial infec-

tions, cancers and cardiovascular disease. The

level of UCH-L1 in each of these pools was then

determined and normalized to the level without

the respective substances.


Expected Value

Plasma samples from normal controls (NC, n = 50) and from patients with Parkinson’s disease (PD, n = 63) were collected for UCH-L1 assays using the IMR UCH-L1 reagent.

Item tested Mean of measured
UCH-L1
concentrations
(pg/ml)
Standard deviation (%CV)
Repeatability Within-Lab
pool 1 100.40 0.94 (0.9) 7.60 (7.6)
pool 2 10.09 0.34 (3.4) 0.51 (5.0)
Precision testing was determined according to CLSI/NCCLS document EP5-A3.
Substance Amount Added Unit % Recovery (Spike/control × 100)
Hemoglobin 10000 μg/ml 104.0
Conjugated bilirubin 600 μg/ml 102.2
Intra lipid 30000 μg/ml 103.7
Uric acid 200 μg/ml 105.2
Rheumatoid factor 500 IU/ml 98.7
Albumin 60000 μg/ml 103.8
Acetylsalicylic acid 500 μg/ml 95.2
Ascorbic acid 300 μg/ml 107.9
Ampicillin sodium 1000 μg/ml 104.2
Quetiapine fumarate 100 ng/ml 103.2
Galantamine hydrobromide 90 ng/ml 98.6
Rivastigmine hydrogen tartrate 100 ng/ml 104.2
Donepezil hydrochloride 1000 ng/ml 100.3
Memantine hydrochloride 150 ng/ml 96.5
Interference testing was based on the principle of CLSI/NCCLS document EP7-A2.

Ordering Information

Order Information
Item (Cat. No.)
Package Size
· UCH-L1 IMR Reagent (MF-UCH-0060)
4 × 1 mL (64 tests)
· UCH-L1 Control Solution (CL-UCH-000T, CL-UCH-100T)
1 mL
· Calibrator-60 (CA-DEX-0060)
1 mL
· Sample testing tubes (MQ-TUB-0100)
100 tubes
· Magnetic Immunoassay Analyzer (XacPro-S361)
161 × 91 × 138 cm
Please contact us for customizable products and more information.