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>   Home   >   Products   >   Primary Antibodies   >   ACTA1 (2B10) Mouse mAb   

ACTA1 (2B10) Mouse mAb

 
Catalog #
ABZ3926
Application
WB, IF, IP, ICC, IHC-F, IHC-P
Uniprot Id
P68133
Reactivity
Human, Mouse, Rat
Isotype
IgG
 
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  • Immunohistochemistry analysis of paraffin-embedded rat liver tissue using alpha Skeletal Muscle Actin (2B10) antibody.High-pressure and temperature Sodium Citrate pH 6.0 was used for antigen retrieval.Negative control was used by secondary antibody only.
  • Western blot analysis of alpha Skeletal Muscle Actin (2B10) in T47D, 3T3, COS7, C6 and Hela lysates using alpha Skeletal Muscle Actin (2B10) antibody
 Catalog #AvailabilitySizeQuantityUnit Price Save For Later Wish List
ABZ3926-100 2 weeks 100 µL $499.00
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ABZ3926-20 2 weeks 20 µL $149.00
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Product Overview

NameACTA1 (2B10) Mouse mAb
Accession (Primary)P68133
Host SpeciesMouse
ClonalityMonoclonal
IsotypeIgG
Species Reactivity
Reacts WithHuman, Mouse, Rat
Calculated MW
Calculated MW: 42 kDa; Observed MW: 42 kDa
Buffer System
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide, pH 7.3.
Storage
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Recommended Dilution
WB-1:500-1:1000; IHC-1:50-1:100; IF-1:50-1:200; IP-1:20
Purification
Affinity Purified
Conjugation
Unconjugated
Modification
Unmodified
Form
Liquid
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 a variety of myopathies, including nemaline myopathy, 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 with manifestations such as hypotonia.

Target Information: ( P68133 )

NameACTA1
Gene ID58
Other Names
ACTA1; ACTA; Actin,alpha skeletal muscle; Alpha-actin-1
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