ACTA1 Recombinant Rabbit Monoclonal Antibody (4C1), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | FEMA550196-Each-of-1 | In Stock | ₹ 37,202.00 |
FEMA550196 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 37,202.00
GST (18%): ₹ 6,696.36
Total Price: ₹ 43,898.36
Antigen
ACTA1
Classification
Recombinant Monoclonal
Concentration
0.28 mg/mL
Formulation
PBS with 50% glycerol and 0.02% sodium azide, pH 7.4
Gene Accession No.
P68133
Gene Symbols
ACTA1
Immunogen
A synthesized peptide derived from Human ACTA1
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
Applications
ELISA, Flow Cytometry, Immunohistochemistry (Paraffin)
Clone
4C1
Conjugate
Unconjugated
Gene
ACTA1
Gene Alias
AA959943, ACTA, Acta1, Acta-2, actin alpha 1, actin alpha 1, skeletal muscle, actin, alpha 1, skeletal muscle, actin, alpha skeletal muscle, Actin, alpha skeletal muscle, intermediate form, Acts, Actsk-1, alpha actin 1, alpha-actin-1, ASMA, beta actin, CFTD, CFTD1, CFTDM, cytoplasmic beta-actin, LOW QUALITY PROTEIN: actin, alpha skeletal muscle, MPFD, NEM1, NEM2, NEM3, nemaline myopathy type 3, SHPM, skeletal alpha actin, unnamed protein product
Host Species
Rabbit
Purification Method
Affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
58
Content And Storage
-20°C or -80°C if preferred
Isotype
IgG
Related Products
Description
- 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.