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ACTA1 Rabbit mAb

 
Catalog #
ABZ2301
Application
WB, IF, FC, IP, ICC, IHC-F, IHC-P
Uniprot Id
P68133
Reactivity
Human, Mouse, Rat
Isotype
IgG
 
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  • Western blot analysis of Alpha Skeletal Muscle in rat muscle lysates using alpha Skeletal Muscle Actin antibody.
  • Western blot analysis of muscle Actin in Hela lysates using muscle Actin antibody.
  • Immunohistochemistry analysis of paraffin-embedded Human colon cancer using muscle Actin antibody. High-pressure and temperature Sodium Citrate pH 6.0 was used for antigen retrieval.
  • Immunocytochemistry analysis of muscle Actin(green) in Hela using muscle Actin antibody,and DAPI(blue).
 Catalog #AvailabilitySizeQuantityUnit Price Save For Later Wish List
ABZ2301-100 2 weeks 100 µL $499.00
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ABZ2301-20 2 weeks 20 µL $149.00
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Product Overview

NameACTA1 Rabbit mAb
Accession (Primary)P68133
Host SpeciesRabbit
ClonalityMonoclonal
IsotypeIgG
Species Reactivity
Reacts WithHuman, Mouse, Rat
Calculated MW
Calculated MW: 42 kDa; Observed MW: 42 kDa
Buffer System
Liquid in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.
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;alpha Skeletal Muscle Actin
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