| Field | Specification |
|---|---|
| Mfr No | |
| Alternative Names | C14orf141; LTBP3 |
| Assay Time | |
| Assay Type | |
| Detection Range | |
| Product Type | |
| Reactivity | |
| Sample Type(s) | serum, plasma, urine, tissue homogenates, cell lysates, cell culture supernates and other biological fluids |
| Sensitivity | |
| Target | |
| UniProt # |
Scientific background
LTBP2 (Latent Transforming Growth Factor Beta Binding Protein 2) is a growth factor–related marker involved in cellular proliferation, differentiation, or tissue remodeling processes.
Growth factor concentrations can reflect changes in tissue repair, fibrosis, angiogenesis, or tumor microenvironment signaling depending on the specific target and model.
Because many growth factors act locally and are regulated post-transcriptionally, protein quantification can add clarity beyond mRNA-only measurements.
Why it matters
- Quantify LTBP2 (Latent Transforming Growth Factor Beta Binding Protein 2) to compare biological changes across conditions, doses, or time points.
- Generate concentration data from a standard curve to support biomarker and mechanistic studies.
How the ELISA works
Designed for Human samples, this kit uses a The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human LTBP2. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human LTBP2. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human LTBP2, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Human LTBP2 in the samples is then determined by comparing the OD of the samples to the standard curve.. After binding and washing, signal is converted to concentration using a standard curve.
Sample types: serum, plasma, urine, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
- Detection range: 0.32-20 ng/mL
- Sensitivity/LoD: 0.132 ng/mL
- Assay time: 3.5h
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Cellular and Molecular Life Sciences
HIF-1α/LTBP2 axis activate HSCs to promote liver fibrosis by interacting with LOXL1 via the ERK pathway
Frontiers in Pharmacology
Latent Transforming Growth Factor-β Binding Protein-2 Regulates Lung Fibroblast-to-Myofibroblast Differentiation in Pulmonary Fibrosis via NF-κB Signaling
Annals of Hepatology
Integrated analyses and a novel nomogram for the prediction of significant fibrosis in patients