Human HSPG2 (Basement membrane-specific heparan sulfate proteoglycan core protein) ELISA Kit
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name
Human HSPG2 (Basement membrane-specific heparan sulfate proteoglycan core protein) ELISA Kit
category
ELISA Kits
provider
FineTest
reference
EH0955
tested applications
ELISA
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | ELISA Kits |
| Reactivity | Human |
| Detection Method | Colorimetric |
| Assay Data | 4 hours |
| Assay Type | Sandwich ELISA, Double Antibody |
| Test Range | 0.625-40ng/ml |
| Sensitivity | 0.375ng/ml |
| Size 1 | 96T |
| Tested Applications | ELISA |
| Sample Type | Serum, Plasma, Cell Culture Supernatant, cell or tissue lysate, Other liquid samples |
| Availability | Shipped within 10-14 working days. |
| Storage | 2-8 °C for 12 months |
| UniProt ID | P98160 |
| Alias | PLC,SJA,SJS,HSPG,SJS1, PRCAN,HSPG,Perlecan,Basement membrane-specific heparan sulfate proteoglycan core protein,Schwartz-Jampel syndrome 1,chondrodystrophic myotonia |
| Background | Elisa kits for HSPG2 |
| Status | RUO |
Heparan sulfate proteoglycan 2 (HSPG2), also known as perlecan, is a significant component of the extracellular matrix (ECM) in many tissues, including basement membranes. HSPG2 plays a crucial role in various physiological processes such as cell adhesion, proliferation, differentiation, and migration. It is synthesized as a large multidomain protein and is extensively glycosylated. Perlecan is ubiquitous in the body, present in vascular endothelial cells, the central nervous system, skeletal muscle, and other tissues. Its importance is underscored by its involvement in numerous developmental and pathological conditions, including cancer, cardiovascular diseases, and genetic disorders like Schwartz-Jampel syndrome and Dyssegmental Dysplasia Silverman-Handmaker type.
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