LRRC57 Polyclonal Antibody
SKU: E-AB-11371-200
LRRC57 Polyclonal Antibody
| SKU # | E-AB-11371 |
| Reactivity | Human, Mouse, Rat |
| Host | Rabbit |
| Applications | IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | IHC |
| Clonality | Polyclonal |
| Immunogen | Recombinant protein of human LRRC57 |
| Abbre | LRRC57 |
| Synonyms | AA407405, DKFZp686H1865, FLJ36812, LRC57, Leucine rich repeat containing 57, Leucine rich repeat containing protein 57, Leucine-rich repeat-containing protein 57, MGC109337, lrrc57 |
| Swissprot | |
| Cellular Localization | Extracellular region or secreted, extracellular exosome, Other locations: membrane. |
| Concentration | 0.2 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cell Biology |
| 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
LRRC57 (leucine rich repeat containing 57) is a 239 amino acid protein that contains eight LRR repeats and is encoded by a gene that maps to human chromosome 15q15.2. Chromosome 15 houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.