Scientific Research Test

Scientific Research Test

The R&D team of New Terrain has been devoted to the research and development of new technologies for the diagnosis of Neuroimmune diseases and Neuroinflammatory disease for many years. These new technologies base on cell-based assay (CBA), immunoblotting technique and immunomagnetic beads and so on. We hope to use our advanced detection methods to improve the diagnosis and treatment of neuroimmune diseases, improve the quality of life of patients, and reduce the social burden.

Service

Neuromuscular junction disease

Myasthenia gravis (MG)

Lambert-Eaton syndrome

CNS diseases

Autocephalus (AE)

Marginal lobe encephalitis (LE)

Optic neuromyelitis (NMO)

Multiple sclerosis (MS)

Peripheral nervous system disease

Guillain-barre syndrome (GBS)

Miller fisher syndrome

Polyneuropathy

Neurological paraneoplastic syndrome

Paraneoplastic syndrome (PNS)

Neuroimmunological Research Services

Neuroimmunological Research Services
Project name
Oligoclonal bands
Detection method
Immunoelectrophoresis
Samples
Serum (2-3ml) without anticoagulant tube, and cerebrospinal fluid (2-3ml)
Project name
AQP4 (Anti-Aquaporin 4)
MOG (myelin oligodendrocyte glycoprotein)
MBP (myelin basic protein)
Detection method
Cell-based assay (CBA)
Samples
Serum (2-3ml) without anticoagulant tube, and cerebrospinal fluid (2-3ml)
Project name
NMDAR (N-methyl-D-aspartate receptor)
AMPA1 (GluA1, glutamate receptor A1)
AMPA2 (GluA2, glutamate receptor A2)
LGI1 (Leucine-rich glioma-inactivated protein 1)
CASPR2 (Contactin-associated protein-like 2)
GABA (γ-Aminobutyric acid receptor)
Detection method
Cell-based assay (CBA)
Samples
Serum (2-3ml) without anticoagulant tube, and cerebrospinal fluid (2-3ml)
Project name
Jo-1、 PL-7、PL-12、 EJ、 SRP、 Mi-2、 MDA-5、 TIF1-γ、 HMGCR、 SSA/Ro52kD SAE-1/2、 NXP-2
Detection method
Western blot
Samples
Serum (2-3ml) without anticoagulant tube
Project name
Hu, Yo, Ri,
CV2(CRMP5) (collapsin response mediator protein 5) collapsin, Ma1(PNMA1) (Paraneoplastic antigen Ma1), Ma2(PNMA2) (Paraneoplastic antigen Ma2), Tr, SOX1, Zic4, GAD65(glutamic acid decarboxylase)
Amphiphysin
Detection method
Western blot
Samples
Serum (2-3ml) without anticoagulant tube, and cerebrospinal fluid (2-3ml)
Project name
GM1、GM2、GM3、GM4、GD1a、GD1b、GD2、GD3
GT1a、GT1b、GQ1b、sulfatides (IgG+IgM)
Detection method
Western blot
Samples
Serum (2-3ml) without anticoagulant tube, and cerebrospinal fluid (2-3ml)
Project name
AchR(Acetylcholine receptor)
Musk(muscle-specific tyrosine kinase)
Detection method
TSA-CBA
Samples
Serum (2-3ml) without anticoagulant tube, and cerebrospinal fluid (2-3ml)
Project name
S100β
Detection method
Immunochromatography of gold magnetic particles
Samples
Serum (1ml) without anticoagulant tube, and cerebrospinal fluid (1ml)
Project name
B-cell assay
Detection method
Flow cytometry: Peripheral blood CD19+%, CD5+CD19+/CD19+, and CD20+% were determined by flow cytometry in rituximab patients.
Samples
EDTA plasma 2-3ml (EDTA anticoagulation tube)
Project name
Type of immune cells (lymphocytes, myeloid cells)
Detection method
The proportion of immune cells in peripheral blood was monitored after immunotherapy
Samples
EDTA plasma 2-3ml (EDTA anticoagulation tube)

Simoa Ultrasensitive Single Molecular Array Cytokine Detection Service

Single-molecule array (Simoa) technology enables ultrasensitive protein detection that is suited to the development of peripheral blood-based assays for assessing neurological disorders. Simoa technology is based on the Quanterix Simoa HD-1 digital single molecular array analyzer, which can directly perform ultra-high sensitivity detection of biomarkers such as proteins and nucleic acids in serum and plasma. The advent of Simoa technology has changed the situation where neural markers could only be detected in cerebrospinal fluid in the past. At present, neurological biomarkers can be detected in peripheral blood using Simoa technology, thus changing the way of diagnosis of brain injury and neurodegenerative diseases. Simoa enables accurate quantitation of soluble immune signaling molecules in an unprecedented femtomolar range. In addition, Simoa technology has also greatly promoted the early detection of cancer, postoperative monitoring and precision medicine. Its main application areas include nerves, tumors, infectious diseases and immune inflammation. At present, there are hundreds of publications citing this technology in the world, including Nature, Science, Cell, Lancet, Nature Biotechnology, The Lancet Neurology, JAMA Neurology, etc.

Mechanisms

A high-level look at a Simoa Bead-based assay, from development to data analysis: (1) Paramagnetic particles coupled with antibodies designed to bind to specific targets are added to the sample. (2) Detection antibodies – capable of generating fluorescent product – are added. (3) The objective is to form an immunocomplex consisting of the bead, bound protein, and detection antibody. (4) At low concentrations, each bead will contain one bound protein, or none. (5) The sample is loaded into arrays, in the Simoa disc, consisting of more than 200,000 microwells – each large enough to hold one bead. (6) Enzymatic signal amplification with fluorescent substrate, fluorescence imaging and data reduction. (7) Data analysis – results can be viewed and analyzed on the board or exported to commonly used software packages or LIMS systems.

Advantages
High sensitivity

More than 1000 times more sensitive than ELISA

Full-automation

Ensure repeatability and accuracy of results

Multiplex detection

Detect multiple target molecules each time

High precision

Coefficient of variation (CVs) of the experimental results are usually less than 10%

Wide linear range

Detection dynamic range more than 4 orders of magnitude

Homebrew capabilities

Using simple, well-established chemistry, researchers can explore significant unmet needs in life science research using digital biomarker analysis technology

Biomarkers list
BiomarkersSpeciesLoD (pg/ml)Median (pg/ml)Sample
BDNFHuman0.01111306C, E, S
TauHuman0.0191.65C, E, S
NF-lightHuman0.0385.33C, E, S
Aβ42Human0.0444.7C, E
GFAPHuman0.21188C, E, S
Aβ40Human0.52265.97C, E
MMP-9Human0.581N/AC, E, S
p-Tau231Human0.621N/AC
pNF-heavyHuman0.66330.82C, E, S
α-SynucleinHuman0.9554145C, E, S
UCH-L1Human1.059.51C, E, S
NSEHuman1.2967845C, E, S
TDP-43Human2.48N/AC, E, S
TauMouse0.61526.7C, E, S

C=CSF, E=EDTA plasma, S=serum

BiomarkersSpeciesLoD (pg/ml)Median (pg/ml)Sample
GM-CSFHuman0.00190.0865E, S
IL13Human0.0020.039E, S
IFN-αHuman0.00250.0036E, S
IL-15Human0.0033.23E, S
IL-10Human0.00380.94E, S
IL-1αHuman0.0040.0293E, S
IL-5Human0.0040.22E, S
IL-17AHuman0.00420.124E, S
IL-4Human0.00460.024E, S
IL-12p70Human0.00481.95E, S
IL-22(Total)Human0.00547.16E, S
IL-6Human0.00551.73E, S
TRAILHuman0.008323.1E, S
IL36βHuman0.010.426E, S
IFN-γHuman0.01040.333E, S
IL-2Human0.0110.086E, S
C-PeptideHuman0.0131559E, S
LIFHuman0.0150.412E, S
IL-1βHuman0.0160.058E, S
IL-12p40/IL-23Human0.0251.3E, S
IL-28AHuman0.0220.303E, S
TGFαHuman0.0313.34E, S
MIP-1βHuman0.03466.7E, S
CCL-11Human0.04N/AE, S
IP-10Human0.052105E, S
IL-8Human0.0565.31E, S
IL-17CHuman0.0651.66E, S
MCP-3Human0.1240.445E, S
IL-23Human0.1320.31E, S
HE4/WFDC2Human0.135104E, S
TGF-βHuman0.1370.31E, S
IL-3Human0.2260.279E, S
IL33Human0.325.45E, S
CEAHuman0.4861511.5E, S
MMP-9Human0.581N/AE, S
Cathepsin SHuman0.76566E, S
LeptinMouse2.466083E, S
IL-1βMouse0.0040.201E, S
IL-1αMouse0.00851.063E, S
IL17A/FMouse0.02211.58E, S
GM-CSFMouse0.032N/AE, S
IL-23Mouse0.0334.89E, S
IL-6Mouse0.03516E, S
IL-17AMouse0.08833.76E, S
IL-22Mouse0.095273.3E, S
IL-17FMouse0.10211.01E, S
TGFαMouse0.13222.6E, S

C=CSF, E=EDTA plasma, S=serum