α-SMA rabbit pAb

α-SMA rabbit pAb

AO-06-ES3850-100

α-SMA rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES3850
Product nameα-SMA rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameACTA1; ACTA; Actin, alpha skeletal muscle; Alpha-actin-1; ACTA2; ACTSA; ACTVS; GIG46; Actin, aortic smooth muscle; Alpha-actin-2; Cell growth-inhibiting gene 46 protein; ACTC1; ACTC; Actin, alpha cardiac muscle 1; Alpha-cardiac actinACTA1; ACTA; Actin, alpha skeletal muscle; Alpha-actin-1; ACTA2; ACTSA; ACTVS; GIG46; Actin, aortic smooth muscle; Alpha-actin-2; Cell growth-inhibiting gene 46 protein; ACTC1; ACTC; Actin, alpha cardiac muscle 1; Alpha-cardiac actin
Size100μL
Unit price ($)248
Human gene ID59
Human Swiss-ProtP68133
SourceRabbit
IsotypeIgG
TargetActin skeletal muscle α
Fields
Gene nameACTA1/ACTA2/ACTC1
Protein nameActin alpha skeletal muscle/Actin aortic smooth muscle/Actin alpha cardiac muscle 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID11459
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP68134
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID29437
Rat gene linkView Rat Gene
Rat Swiss-ProtP68136
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from the C-terminal region of human α-SMA.
Specificityα-SMA Polyclonal Antibody detects endogenous levels of α-SMA protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. IHC-p: 1:100-300 ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)42kD
BackgroundThe 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, Jul 2008],
Functiondisease:Defects in ACTA1 are a cause of congenital myopathy with excess of thin myofilaments (CM) [MIM:102610].,disease:Defects in ACTA1 are a cause of congenital myopathy with fiber-type disproportion (CFTD) [MIM:255310]; also known as congenital fiber-type disproportion myopathy (CFTDM). CFTD is a genetically heterogeneous disorder in which there is relative hypotrophy of type 1 muscle fibers compared to type 2 fibers on skeletal muscle biopsy. However, these findings are not specific and can be found in many different myopathic and neuropathic conditions.,disease:Defects in ACTA1 are the cause of nemaline myopathy type 3 (NEM3) [MIM:161800]. Nemaline myopathy (NEM) is a form of congenital myopathy characterized by abnormal thread- or rod-like structures in muscle fibers on histologic examination. The clinical phenotype is highly variable, with differing age at onset and severity.,func
Subcellular locationCytoplasm, cytoskeleton.
ExpressionEpithelium,Skeletal muscle,

Additional Images

Image 1
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Western Blot analysis of MFC cells using α-SMA Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunohistochemical analysis of paraffin-embedded rat-muscle, antibody was diluted at 1:100
Image 3
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Immunohistochemical analysis of paraffin-embedded rat-muscle, antibody was diluted at 1:100
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Immunohistochemical analysis of paraffin-embedded mouse-muscle, antibody was diluted at 1:100
: AO-06-ES3850-100
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