Myosin Binding Protein C, Slow Type (MYBPC1) 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, Slow Type (MYBPC1) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx336653

Description

MYBPC1 Antibody (FITC) is a Rabbit Polyclonal against MYBPC1.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Myosin Binding Protein C, Slow Type (MYBPC1)
Host
Rabbit
Reactivity
Human
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
FITC
Isotype
IgG
Purity
> 95%
Purification
Purified by Protein G.
Size 1
20 µg
Size 2
50 µg
Size 3
100 µg
Size 4
200 µg
Size 5
1 mg
Form
Liquid
Buffer
0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q00872
Gene ID
4604
Alias
LCCS4,CMYP16,MYBPCC,MYBPCS,MYOTREM,ssMyBP-C,Slow MyBP-C,C-protein skeletal muscle slow isoform
Background
Antibody anti-MYBPC1
Status
RUO

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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