ACTA1 Mouse anti-Human, Clone: 3B3, Abnova™
Manufacturer: Abnova Corporation
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | 89-933-511-Each-of-1 | In Stock | ₹ 85,173.00 |
89-933-511 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 85,173.00
GST (18%): ₹ 15,331.14
Total Price: ₹ 1,00,504.14
Antigen
ACTA1
Classification
Monoclonal
Conjugate
Unconjugated
Dilution
ELISA Immunohistochemistry (Frozen sections) (1:100-1:1000) Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (10 ug/mL) Western Blot (1:1000-1:5000) The optimal working dilution should be determined by the end user.
Gene Alias
ACTA/ASMA/CFTD/CFTD1/CFTDM/MPFD/NEM1/NEM2/NEM3
Host Species
Mouse
Purification Method
Protein G purification
Regulatory Status
RUO
Gene ID (Entrez)
58
Content And Storage
Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.
Isotype
IgG1
Applications
ELISA, Immunohistochemistry (Frozen), Immunohistochemistry (PFA fixed), Western Blot
Clone
3B3
Description
Mouse monoclonal antibody raised against human ACTA1.
Formulation
In PBS (0.09% sodium azide).
Gene Symbols
ACTA1
Immunogen
A synthetic peptide corresponding to N-terminus region of human ACTA1.
Quantity
50 μg
Primary or Secondary
Primary
Target Species
Human
Form
Liquid
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
- [provided by RefSeq] Sequence: DEDETTALVC