TPM2 Polyclonal Antibody Store at -20°C
SKU: E-AB-12435-200
TPM2 Polyclonal Antibody Store at -20°C
| SKU # | E-AB-12435 |
| Reactivity | Human |
| Host | Rabbit |
| Applications | WB, IHC |
Product Details
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Immunogen | Synthetic peptide of human TPM2 |
| Abbre | TPM2 |
| Synonyms | AMCD1, Alpha tropomyosin, Arthrogryposis multiplex congenital distal type 1, Beta tropomyosin, Beta-tropomyosin, Cytoskeletal tropomyosin TM30, DA1, DA2B, FLJ41118, HEL-S-273, HTM al, Heat stable cytoskeletal protein 30 kDa, epididymis secretory protein Li 273, hscp30 |
| Swissprot | |
| Calculated MW | 33 kDa |
| Cellular Localization | Cytoplasm>cytoskeleton. |
| Concentration | 0.4 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | 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 |
| WB | 1:500-1:2000 |
| IHC | 1:50-1:200 |
Background
This gene encodes beta-tropomyosin, a member of the actin filament binding protein family, and mainly expressed in slow, type 1 muscle fibers. Mutations in this gene can alter the expression of other sarcomeric tropomyosin proteins, and cause cap disease, nemaline myopathy and distal arthrogryposis syndromes. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. TPM2 has been shown to interact with RRAD, PDLIM7 and TPM1.