Proteintech beta Actin Mouse anti-Hamster, Human, Mouse, Non-human primate, Rat, Zebrafish, Clone: 2D4H5, Proteintech

Mouse Monoclonal Antibody

Additional Details:
Additional Details: Weight: 0.00010kg



Product Code. 16817505

Quantity Price
1 189.0  € / 150µL
In stock, ready to ship: 25
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Description and Specification

Specification

Antigen beta Actin
Applications Flow Cytometry,Immunocytochemistry,Immunofluorescence,Immunohistochemistry (Paraffin),Immunoprecipitation
Classification Monoclonal
Clone 2D4H5
Concentration 0.43 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.02% sodium azide; pH 7.3
Gene ACTA1
Gene Accession No. P48975, P60709, P60710, P60711, P62736, P62737, P62738, P63259, P63260, P63261, P63267, P63268, P63269, P68032, P68033, P68035, P68133, P68134, P68136
Gene Alias ACTB, Actin, actin, beta, Actin, cytoplasmic 1, B actin, Beta actin, F actin, PS1TP5BP1
Gene Symbols ACTA1, acta1b, acta2, ACTB, actb1, ACTC1, actc1b, Actg1, ACTG2
Host Species Mouse
Purification Method Protein A
Quantity 150 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 100689477, 100758575, 100764022, 100766388, 100768744, 100768972, 11459, 11461, 11464, 11465, 11468, 11475, 25365, 287876, 29275, 29437, 322509, 407658, 57934, 58, 58114, 59, 60, 70, 71, 72, 81633, 81822
Target Species Hamster,Human,Mouse,Non-human Primate,Rat,Zebrafish
Content And Storage -20°C
Product Type Antibody
Form Liquid
Isotype IgG2b

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.