Myosin Binding Protein C, Cardiac (MYBPC3) Antibody (FITC)

Este producto es parte de MYBPC - myosin binding protein C
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169€ (20 µg)

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935106861
info@markelab.com
name
Myosin Binding Protein C, Cardiac (MYBPC3) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx107594

Description

Myosin-binding protein C, cardiac-type Antibody (FITC) is a Rabbit Polyclonal antibody against Myosin-binding protein C, cardiac-type conjugated to FITC.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetMyosin Binding Protein C, Cardiac (MYBPC3)
HostRabbit
ReactivityRat
Recommended DilutionOptimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationFITC
IsotypeIgG
Purity> 95%
PurificationPurified by Protein G.
Size 120 µg
Size 250 µg
Size 3100 µg
Size 4200 µg
Size 51 mg
FormLiquid
Buffer0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDP56741
Gene ID295929
AliasFHC,CMH4,CMD1MM,LVNC10,MYBP-C,cMyBP-C,C-protein cardiac muscle isoform,Cardiac MyBP-C,Myosin-binding protein C, cardiac-type
BackgroundAntibody anti-MYBPC3
StatusRUO

Descripción

MYBPC3 is a crucial component of the sarcomere in cardiac muscles, where it regulates cardiac contractility and stabilizes the structural framework of the thick filament. Through its interactions with myosin and actin, it modulates the force and efficiency of cardiac muscle contraction, playing a central role in maintaining the heart’s mechanical function. Mutations in MYBPC3 are a common genetic cause of hypertrophic cardiomyopathy (HCM), a condition characterized by the abnormal thickening of the heart muscle that can lead to heart failure and arrhythmias. These mutations often result in impaired sarcomere function and contribute to maladaptive cardiac remodeling. Research on MYBPC3 focuses on its role in cardiomyopathy pathogenesis and its potential as a therapeutic target for improving heart function in affected individuals.

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