| Field | Specification |
|---|---|
| Target | |
| Species | |
| Reactivity | |
| Applications | |
| Assay type | |
| Sample type(s) | serum, plasma, tissue homogenates |
| Sensitivity | |
| Detection range | |
| Detection wavelength | |
| Assay time | |
| Catalog no. (Mfr.) | |
| Main SKU |
Background
Hyaluronic acid (HA) is a biological molecule commonly studied in cell biology research. It is commonly used as a molecular readout in mechanistic and biomarker-focused studies.
Biological context
Researchers often monitor Hyaluronic acid in serum, plasma, and tissue homogenates to better understand themes such as signal transduction pathways, cell cycle control, and stress-response programs. In many model systems, measured levels can shift with physiology, experimental perturbation, or disease-associated changes, making careful biological interpretation important.
Interpreting changes in measured levels
Depending on sample matrix and study design, increases or decreases in Hyaluronic acid may reflect differences in expression, secretion, turnover, or compartmentalization rather than a single mechanism. Interpretation is typically strengthened by evaluating related molecules (for example, phosphorylation-dependent signaling nodes, stress markers, and organelle proteins) and by keeping pre-analytical variables consistent across groups.
Why ELISA data are widely used
ELISA is a common approach for quantitative measurement of proteins and biomarkers in complex samples, enabling comparisons across experimental groups and time points. When integrating results with other readouts, consider species biology, sample type, and the broader pathway context that Hyaluronic acid participates in.
Can’t Find What You’re Looking For? We can help you source the best match or customize an ELISA solution for your study. Options may include alternative target synonyms, different species reactivity, sample type/matrix compatibility (serum/plasma/lysate/supernatant), assay format (sandwich/competitive), sensitivity/range, detection chemistry (colorimetric/fluorescent/chemiluminescent), plate format (pre-coated/uncoated, strips vs full plate), and bulk or custom packaging. Click Talk to a Scientist to submit a request form, email us at support@biohippo.com, or explore our Research Services for additional support. Our team will be in contact with you shortly.
Targeting hyaluronan synthesis enhances the therapeutic effectiveness of biologics in inflammatory bowel disease
P Xiao, Z Chen, X Cai, W Xia, X Liu, Z Song,JCI insight,2025
Идиопатический легочный фиброз (ИЛФ)
АА Ярославцева,/,2024
Dietary supplementation with α-ionone alleviates chronic UVB exposure-induced skin photoaging in mice
R Geng,Food & function,2024
Dietary Isoeugenol Supplementation Attenuates Chronic UVB-Induced Skin Photoaging and Modulates Gut Microbiota in Mice
Y Chen,Nutrients,2024
Revitalizing Photoaging Skin through Eugenol in UVB-Exposed Hairless Mice: Mechanistic Insights from Integrated Multi-Omics
F Feng,Antioxidants,2024
Farnesoid X receptor activation is required for the anti-inflammatory and anti-oxidative stress effects of Alisol B 23-acetate in carbon tetrachloride-induced liver fibrosis in mice
L Zhang,International immunopharmacology,2023
Anti-inflammatory and Antifibrotic Potential of Longidaza in the Bleomycin-induced Pulmonary Fibrosis
A Pakhomova,/,2023
Xiaochaihu decorction relieves liver fbrosis caused by Schistosoma japonicum infection via the HSP47/TGF-β pathway
Y Huang,Parasit Vectors,2020
Combination leflunomide and methotrexate impedes the recovery of liver fibrosis, partly through inhibition of myeloid cell admittance
Mengxin Lin, et al,Molecular Medicine Reports,2019
A Polysaccharide from Amusium Pleuronectes Combined with Praziquantel Treatment Ameliorates Hepatic Fibrosis in Schistosoma Japonicum-Infected Mice
Tang X.et al,Med Sci Monit,2018
Toxoplasma gondii GRA15II effector-induced M1 cells ameliorate liver fibrosis in mice infected with Schistosomiasis japonica.
Xie Y.et al,Cell Mol Immunol.,2016
Role of Hematopoietic Stem Cells in Inflammation of the Pancreas during Diabetes Mellitus.
Dygai AM.et al,Bull Exp Biol Med.,2016