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Actin, Muscle Specific (ABT-MSA) IHC kit

-IHCM6142

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Catalog: IHCM6142
Size
Price
Status
Qty.
100mL
$2,960.00
3 weeks

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10mL
$356.00
3 weeks

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3mL
$156.00
3 weeks

0

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Main Information
Target

Actin_Muscle Specific

Host Species

Mouse

Reactivity

Human, Mouse, Rat, Monkey, Bovin, Pig, Chick,

Applications

IHC

Conjugate/Modification


Unmodified

Detailed Information
Specificity
The antibody can specifically recognize proteins from smooth muscle, myocardium and skeletal muscle α actin and smooth muscle derived γ actin, and β actin or non smooth muscle derived γ actin does not respond.
Purification
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage
2°C to 8°C/1 year
Modification
Unmodified
Clonality
Monoclonal
Clone Number
ABT-MSA
Isotype
IgG1,Kappa
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human Actin, Muscle Specific AA range: 2-50
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Specificity:
The antibody can specifically recognize proteins from smooth muscle, myocardium and skeletal muscle α actin and smooth muscle derived γ actin, and β actin or non smooth muscle derived γ actin does not respond.
show all
Gene Name:
Actin, Muscle Specific
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Protein Name:
Actin, Muscle Specific
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Database Link:
Organism Gene ID SwissProt
Human P68032;P68133;P63267;P62736;
Background:
Actins are highly conserved proteins that are involved in various types of cell motility. Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to four others. The protein encoded by this gene belongs to the actin family which is comprised of three main groups of actin isoforms, alpha, beta, and gamma. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. Defects in this gene have been associated with idiopathic dilated cardiomyopathy (IDC) and familial hypertrophic cardiomyopathy (FHC). [provided by RefSeq, Jul 2008],
Function:
Disease:Defects in ACTC1 are the cause of cardiomyopathy dilated type 1R (CMD1R) [MIM:102540]. Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death.,Disease:Defects in ACTC1 are the cause of cardiomyopathy familial hypertrophic type 11 (CMH11) [MIM:612098]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.,Function:Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells.,miscellaneous:In vertebrates 3 main groups of actin isoforms, alpha, beta and gamma have been identified. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins coexist in most cell types as components of the cytoskeleton and as mediators of internal cell motility.,similarity:Belongs to the actin family.,subunit:Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to 4 others.,
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Cellular Localization:
Cytoplasmic
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Tissue Expression:
Muscle,Tongue,
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Research Areas:
>>Cardiac muscle contraction ;
>>Adrenergic signaling in cardiomyocytes ;
>>Hypertrophic cardiomyopathy ;
>>Dilated cardiomyopathy
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Catalog: IHCM6142
Size
Price
Status
Qty.
100mL
$2,960.00
3 weeks

0

10mL
$356.00
3 weeks

0

3mL
$156.00
3 weeks

0

Add to cart

Collected

Collect

Customized Service

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