Actin Muscle Monoclonal Antibody (MSA06 (HUC1-1)), Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIMA511874-Each-of-1 | In Stock | ₹ 38,715.00 |
PIMA511874 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 38,715.00
GST (18%): ₹ 6,968.70
Total Price: ₹ 45,683.70
Antigen
Actin Muscle
Classification
Monoclonal
Concentration
0.2 mg/mL
Formulation
PBS with 0.2% BSA and 0.09% sodium azide; pH 7.4
Gene Accession No.
P62739, P68138, Q3ZC07, P62736, P68032, P68133, P62737, P68033, P68134, P68137, P62738, P68035, P68136
Gene Symbols
ACTA1, ACTA2, ACTC1
Immunogen
Purified actin
Quantity
500 μL
Primary or Secondary
Primary
Target Species
Bovine, Canine, Equine, Human, Mouse, Porcine, Rat
Product Type
Antibody
Isotype
IgG1 κ
Applications
Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
Clone
MSA06 (HUC1-1)
Conjugate
Unconjugated
Gene
ACTA2
Gene Alias
actin, alpha skeletal muscle, alpha skeletal muscle actin, alpha-actin-1, alpha-sma
Host Species
Mouse
Purification Method
Protein G
Regulatory Status
RUO
Gene ID (Entrez)
100057678, 100062175, 100065454, 100152267, 100154254, 11459, 11464, 11475, 281592, 29275, 29437, 477587, 478250, 488984, 515610, 533219, 58, 59, 70, 733615, 81633
Content And Storage
4° C
Form
Liquid
Related Products
Description
- This antibody reacts with alpha-smooth muscle, alpha-skeletal and alpha-cardiac (sarcomeric)
- This pan muscle actin antibody reacts with tumors arising from smooth muscle (leiomysarcomas) as well as skeletal muscle tumors (rhabdomyosarcomas)
- 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.