Human TREM2 ELISA Kit is a single-wash 90-min SimpleStep Sandwich ELISA used to quantify Human TREM2 with a sensitivity of 10.5 pg/mL. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.
- Colorimetric sandwich ELISA - 450 nm readout, works on any plate reader
- Validated on a number of sample types including cerebrospinal fluid (CSF)
- Need to design your own assay: we also offer the conjugation-ready antibody pair
- Cited in over 10 publications
Application | Reactivity | Dilution info | Notes |
---|---|---|---|
Application sELISA | Reactivity Reacts | Dilution info - | Notes - |
The protein expressed by gene TREM2 forms a receptor signaling complex with TYROBP, facilitating signaling and cell activation upon ligand binding. It serves as a receptor for amyloid-beta protein 42, mediating its uptake and degradation by microglia, and also acts as a receptor for lipoprotein particles such as LDL, VLDL, HDL, and various apolipoproteins, enhancing their uptake in microglia. TREM2 binds phospholipids, preferably anionic lipids, and is necessary for microglial phagocytosis of apoptotic neurons. It regulates changes in microglial numbers with age and activates immune responses in macrophages and dendritic cells, where it plays a role in chemokine receptor CCR7 up-regulation, as well as dendritic cell maturation and survival. Additionally, TREM2 is involved in positively regulating osteoclast differentiation. This supplementary information is collated from multiple sources and compiled automatically.
Triggering receptor expressed on myeloid cells 2, TREM-2, Triggering receptor expressed on monocytes 2, TREM2
Human TREM2 ELISA Kit is a single-wash 90-min SimpleStep Sandwich ELISA used to quantify Human TREM2 with a sensitivity of 10.5 pg/mL. The assay uses a simple mix-wash-read protocol with just one incubation and one wash step.
- Colorimetric sandwich ELISA - 450 nm readout, works on any plate reader
- Validated on a number of sample types including cerebrospinal fluid (CSF)
- Need to design your own assay: we also offer the conjugation-ready antibody pair
- Cited in over 10 publications
Sample | n | C.V. |
---|---|---|
Sample Serum | n 5 | C.V. 6.3 |
Sample | n | C.V. |
---|---|---|
Sample Serum | n 3 | C.V. 4.9 |
Sample type | Average % | Range |
---|---|---|
Sample type Serum | Average % = 93 | Range 85 - 104 % |
Sample type EDTA Plasma | Average % = 101 | Range 93 - 105 % |
Sample type Cerebral Spinal Fluid | Average % = 111 | Range 109 - 113 % |
Sample type Cell culture extracts | Average % = 109 | Range 100 - 117 % |
Sample type Cell culture media | Average % = 91 | Range 86 - 94 % |
Sample type Tissue Extracts | Average % = 99 | Range 95 - 101 % |
Sample type Heparin Plasma | Average % = 103 | Range 97 - 111 % |
Sample type Citrate plasma | Average % = 95 | Range 90 - 103 % |
Human TREM2 ELISA Kit ab224881 is a rapid single-wash 90-min ELISA kit to measure Human TREM2 in cerebral spinal fluid (CSF), cell culture extracts, tissue extracts, cell culture media, serum and plasma. This SimpleStep ELISA® sensitivity is 10.5 pg/mL.
How the assay works
Human TREM2 SimpleStep ELISA® employs capture antibodies conjugated to an affinity tag that is recognized by the monoclonal antibody used to coat our SimpleStep ELISA® plates. This approach to sandwich ELISA allows the formation of the antibody-analyte sandwich complex in a single step, significantly reducing assay time. See the SimpleStep ELISA® protocol summary in the image section for further details.
Assay Specificity
This kit recognizes both native and recombinant Human TREM2 protein in serum, plasma, cerebrospinal fluid and cell culture supernatant, cell and tissue extract samples only.
Human TREM2 ELISA Kit ab224881 protocol summary:
1. Mix: add samples/standards to the wells together with the capture and detector antibody cocktail. Incubate for 1 hr at room temperature
2. Wash
3. Add TMB development solution - incubate for 10 min
4. Add stop solution
5. Read the results on a plate reader at 450nm
How other researchers are using Human TREM2 ELISA kit ab224881
Human TREM2 ELISA kit ab224881has been used to study the blood brain barrier disruption in anti-NMDA receptor encephalitis(1) and to study TREM2 expression in plasma and CSF of Alzheimer disease patients(2).
References:
(1)Haoxiao Chang et al. 2023, PMID: 37481571,Save your precious samples
Our 384-well Human TREM2 ELISA Kit only requires a maxmum of 12.5µL
Design your own immunoassay
We offer the antibody pair used in this kit in a BSA and Azide-free format, ready for conjugation
- Human TREM2 Antibody Pair - BSA and Azide free Human TREM2 Antibody Pair - BSA and Azide free ab244027
- Anti-TREM2 antibody [EPR20243-78] - BSA and Azide free (Capture) Anti-TREM2 antibody [EPR20243-78] - BSA and Azide free (Capture) ab244673
- Anti-TREM2 antibody [EPR20243-269] - BSA and Azide free (Detector) Anti-TREM2 antibody [EPR20243-269] - BSA and Azide free (Detector) ab244938
Related and recommended products
Human TREM2 ELISA kit ab224881 is commonly used to measure TREM2 as a marker of neurodegenerative disorders.
Other ELISA kits to study neurodegeneration include:
- Human IL-6 ELISA kit ab17801
- Human CSF-1-R ELISA kit Human CSF-1-R ELISA Kit ab230940
TREM2 is immune receptor expressed on the surface of microglia. TREM2 is proteolytically process by ADAM proteases and the soluble TREM2 is released into the extra cellular space. Elevated levels of soluble TREM2 in cerebrospinal fluid is a biomarker associated with increased risk of Alzheimer's disease. ab224881 TREM2 SimpleStep ELISA® is designed against the extracellular portion of TREM2.
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Interpolated concentrations of native TREM2 in Human cerebrospinal fluid and THP-1 cell culture supernatant samples.
The concentrations of TREM2 were measured in duplicates, interpolated from the TREM2 standard curves and corrected for sample dilution. Undiluted samples are as follows: cerebrospinal fluid 25% and THP-1 cell culture supernatant 12.5%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean TREM2 concentration was determined to be 19.8 ng/mL in cerebrospinal fluid, and 8.4 ng/mL in THP-1 cell culture supernatant.
Example of Human TREM2 standard curve in Sample Diluent NS.
Background-subtracted data values (mean +/- SD) are graphed.
Example of Human TREM2 standard curve in 1X Cell Extraction Buffer PTR. The TREM2 standard curve was prepared as described. Raw data values are shown in the table. Background-subtracted data values (mean +/- SD) are graphed
Example of Human TREM2 standard curve in 1X Cell Extraction Buffer PTR.
Background-subtracted data values (mean +/- SD) are graphed.
Example of Human TREM2 standard curve in Sample Diluent NS. The TREM2 standard curve was prepared as described. Raw data values are shown in the table. Background-subtracted data values (mean +/- SD) are graphed.
Interpolated concentrations of native TREM2 in Human serum and plasma samples.
The concentrations of TREM2 were measured in duplicates, interpolated from the TREM2 standard curves and corrected for sample dilution. Undiluted samples are as follows: serum 12.5%, plasma (EDTA) 12.5%, plasma (heparin) 12.5%, and plasma (citrate) 25%. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean TREM2 concentration was determined to be 23.8 ng/mL in serum, 19.0 ng/mL in plasma (EDTA), 25.3ng/mL in plasma (heparin) and 16.5 ng/mL in plasma (citrate).
Serum from ten individual healthy Human female donors was measured in duplicate.
Interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean TREM2 concentration was determined to be 30 ng/mL with a range of 13 – 66 ng/mL.
Interpolated concentrations of native TREM2 in human THP-1 cell extract and human placenta tissue extract.
The concentrations of TREM2 were measured in duplicate and interpolated from the TREM2 standard curve and corrected for sample dilution and extract load. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). The mean TREM2 concentration was determined to be 15.7 pg/μg in THP-1 cell extract and 0.34 pg/μg in placenta tissue extract.
Linearity of dilution is determined based on interpolated values from the standard curve. Linearity of dilution defines a sample concentration interval in which interpolated target concentrations are directly proportional to sample dilution.
Native TREM2 was measured in the following biological samples in a 2-fold dilution series. Sample dilutions are made in Sample Diluent NS.
Linearity of dilution.
Native TREM2 was measured in the following biological samples in a 2-fold dilution series. Sample dilutions are made in Sample Diluent NS.
Linearity of dilution.
Native TREM2 was measured in the following biological samples in a 2-fold dilution series. Sample dilutions are made in 1X Cell Extraction Buffer PTR.
Example of human TREM2 standard curve in 1X Cell Extraction Buffer PTR in 96-well vs. 384-well plate.
Example of human TREM2 standard curve in 96-well vs. 384-well plate. Background-subtracted data values (mean +/- SD) are graphed.
SimpleStep ELISA technology allows the formation of the antibody-antigen complex in one single step, reducing assay time to 90 minutes. Add samples or standards and antibody mix to wells all at once, incubate, wash, and add your final substrate. See protocol for a detailed step-by-step guide.
Example of human TREM2 standard curve in Sample Diluent NS in 96-well vs. 384-well plate.
Example of human TREM2 standard curve in 96-well vs. 384-well plate. Background-subtracted data values (mean +/- SD) are graphed.
Interpolated concentrations of human TREM2 in THP-1 cell extract in 96-well vs. 384-well plates.
Interpolated concentration of native TREM2 was measured in duplicate at different sample concentrations in 96-well vs. 384-well plates. Undiluted samples are 250 µg/mL THP-1 cell extract. The interpolated dilution factor corrected values are plotted (mean +/- SD, n=2). Sample dilutions are made in 1X Cell Extraction Buffer PTR.
Interpolated concentrations of human TREM2 in human serum in 96-well vs. 384-well plates.
Interpolated concentration of native TREM2 was measured in duplicate at different sample concentrations in 96-well vs. 384-well plates. Undiluted samples are 12.5% human serum. The interpolated dilution factor corrected values (to near sample) are plotted (mean +/- SD, n=2). Sample dilutions are made in Sample Diluent NS.
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