FBN1 Polyclonal Antibody Store at -20°C
SKU: E-AB-12404-200
FBN1 Polyclonal Antibody Store at -20°C
| SKU # | E-AB-12404 |
| Reactivity | Human, Mouse |
| Host | Rabbit |
| Applications | IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide of human FBN1 |
| Abbre | FBN1 |
| Synonyms | 350 kDa glycoprotein component extracellular microfibril, ACMICD, FBN, FBN 1, FBN1, Fibrillin 15, Fibrillin-1, Fibrillin1, Fibrillin15, GPHYSD2, MASS, MFS 1, MFS1, Marfan syndrome, OCTD, SGS, SSKS, WMS, WMS2, Weill Marchesani syndrome |
| Swissprot | |
| Cellular Localization | Secreted>extracellular space>extracellular matrix. |
| Concentration | 0.3 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Signal Transduction |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
Related Reagents
| Applications | Recommended Dilution |
| IHC | 1:50-1:200 |
Background
This gene encodes a member of the fibrillin family. The encoded protein is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated witHuman, Mousearfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.