| Detection range: | 0.312-20ng/mL |
| Sensitivity: | 0.106ng/mL |
| Type: | Traditional COL7 ELISA kit |
| Synonyms: | COL7-A1; COL7A1; EBD1; EBDCT; EBR1; Long-chain collagen; Epidermolysis Bullosa,Dystrophic,Dominant And Recessive; Collagen Alpha-1(VII)chain |
| Species: | Mouse |
| Sample type: | serum, plasma or other biological fluids. |
| Experimental method: | Sandwich |
| Shelf life: | 12 months |
| Gene ID: | 12836 |
| UniProt ID: | Q63870 |
| Components: | 1. Pre-coated, ready to use 96-well strip plate 1 2. Plate sealer for 96 wells 2 3. Standard 2 4. Diluents buffer: 1×45 mL 5. Detection Reagent A: 1×120 μL 6. Detection Reagent B: 1×120 μL 7. TMB Substrate: 1×9 mL 8. Stop Solution: 1×6 mL 9. Wash Buffer (30× concentrate): 1×20 mL |
Background
Predicted to enable collagen binding activity and platelet-derived growth factor binding activity. Acts upstream of or within several processes, including extracellular matrix organization; lung development; and skeletal muscle tissue development. Located in sarcolemma. Is active in several cellular components, including lysosome; myofibril; and sarcoplasmic reticulum. Is expressed in several structures, including alimentary system; brain; genitourinary system; heart and pericardium; and sensory organ. Used to study Bethlem myopathy and Ullrich congenital muscular dystrophy. Human ortholog(s) of this gene implicated in Bethlem myopathy and Ullrich congenital muscular dystrophy 1A. Orthologous to human COL6A1 (collagen type VI alpha 1 chain).
