Myosin Binding Protein C, Slow Type (MYBPC1) Antibody

Este producto es parte de MYBPC - myosin binding protein C
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221€ (50 µg)

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935106861
info@markelab.com
name
Myosin Binding Protein C, Slow Type (MYBPC1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx327613
tested applications
ELISA, WB

Description

MYBPC1 Antibody is a Rabbit Polyclonal against MYBPC1.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetMyosin Binding Protein C, Slow Type (MYBPC1)
HostRabbit
ReactivityHuman, Mouse, Rat
Recommended DilutionELISA: 1/20000, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationUnconjugated
IsotypeIgG
PurificationPurified by affinity chromatography.
Size 150 µg
Size 2100 µg
FormLiquid
Tested ApplicationsELISA, WB
BufferPBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
AvailabilityShipped within 5-10 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ00872
Gene ID4604
AliasLCCS4,CMYP16,MYBPCC,MYBPCS,MYOTREM,ssMyBP-C,Slow MyBP-C,C-protein skeletal muscle slow isoform
BackgroundAntibody anti-MYBPC1
StatusRUO

Descripción

MYBPC1 is a structural protein predominantly expressed in slow-twitch skeletal muscles, where it plays a critical role in maintaining the structural integrity of sarcomeres and regulating muscle contraction. By interacting with myosin and actin filaments, it modulates their binding interactions and stabilizes the thick filaments within the muscle fibers. This ensures the proper alignment and function of the contractile apparatus. Mutations in MYBPC1 have been associated with various myopathies, including those characterized by muscle weakness and reduced contractility, particularly in conditions affecting slow-twitch muscles. These mutations can lead to disruptions in sarcomere assembly and force transmission. MYBPC1’s role in muscle biomechanics makes it an important focus of research into muscle function and disease mechanisms.

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