Rabbit anti-ACTA1 Polyclonal Antibody
| Specifications | |
|---|---|
| Type: | Primary Antibody |
| Clonality: | Polyclonal |
| Host: | Rabbit |
| Reactivity: | Human, Mouse, Rat |
| Isotype: | IgG |
| Label: | Unconjugated |
| Concentration: | 0.5 mg/mL |
| Buffer: | PBS with 0.05% sodium azide and 50% glycerol, PH7.4 |
| Additional Information | |
|---|---|
| Synonyms: | a actin, ACTA, ACTA1, Actin alpha skeletal muscle, Actin, actin, alpha 1, skeletal muscle 1, actin, alpha 1, skeletal muscle, Actin, alpha skeletal muscle, actina, actine, ACTS, aktin, Alpha Actin 1, Alpha skeletal muscle Actin, alpha skeletal muscle, alpha-actin, Alpha-actin-1, ASMA, CFTD, CFTD1, CFTDM, MPFD, NEM1, NEM2, NEM3, nemaline myopathy type 3 |
| UniProt ID: | P68133 |
Applications
WB, IHC, ELISA
Recommended Dilution
WB 1:500-1:2000, IHC 1:50-1:200
Immunogen
Recombinant protein of human ACTA1
Purification/Format
Affinity purification
Background
The product encoded by this gene belongs to the actin family of proteins, which are highly conserved proteins that play a role in cell motility, structure and integrity. Alpha, beta and gamma actin isoforms have been identified, with alpha actins being a major constituent of the contractile apparatus, while beta and gamma actins are involved in the regulation of cell motility. This actin is an alpha actin that is found in skeletal muscle. Mutations in this gene cause nemaline myopathy type 3, congenital myopathy with excess of thin myofilaments, congenital myopathy with cores, and congenital myopathy with fiber-type disproportion, diseases that lead to muscle fiber defects.
- Catalog Number
RD77698A-120-RDB - Supplier
Reddot Biotech - Size
- Shipping
Blue Ice
Price
602,00 €
