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SAB3501005

Sigma-Aldrich

Anti-MYBPC1 antibody produced in rabbit

affinity isolated antibody

Sinônimo(s):

Anti-LCCS4, Anti-MYBPCC, Anti-MYBPCS, Anti-MYOTREM, Anti-ssMyBP-C

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

fonte biológica

rabbit

conjugado

unconjugated

forma do anticorpo

affinity isolated antibody

tipo de produto de anticorpo

primary antibodies

clone

polyclonal

forma

buffered aqueous solution

reatividade de espécies

mouse, human, rat

concentração

1 mg/mL

técnica(s)

ELISA: suitable
immunoblotting: suitable
immunofluorescence: suitable

nº de adesão NCBI

NP_002456

nº de adesão UniProt

Q00872

Condições de expedição

wet ice

temperatura de armazenamento

−20°C

modificação pós-traducional do alvo

unmodified

Informações sobre genes

human ... MYBPC1(4604)

Imunogênio

Antibody was raised against an 18 amino acid synthetic peptide near the amino terminus of human MYBPC1.

Características e benefícios

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Ligação

The action of this antibody can be blocked using blocking peptide SBP3501005.

forma física

Supplied at 1 mg/mL in PBS with 0.02% sodim azide.

Exoneração de responsabilidade

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Código de classe de armazenamento

10 - Combustible liquids

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

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Natasha Ranu et al.
Acta neuropathologica communications, 10(1), 185-185 (2022-12-18)
Nemaline myopathy (NM) is one of the most common non-dystrophic genetic muscle disorders. NM is often associated with mutations in the NEB gene. Even though the exact NEB-NM pathophysiological mechanisms remain unclear, histological analyses of patients' muscle biopsies often reveal
Janelle Geist Hauserman et al.
JCI insight, 6(19) (2021-08-27)
Myosin binding protein-C slow (sMyBP-C) comprises a subfamily of cytoskeletal proteins encoded by MYBPC1 that is expressed in skeletal muscles where it contributes to myosin thick filament stabilization and actomyosin cross-bridge regulation. Recently, our group described the causal association of
Janelle Geist et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, fj201800624R-fj201800624R (2018-06-07)
Myosin binding protein-C slow (sMyBP-C) comprises a family of accessory proteins in skeletal muscles that bind both myosin and actin filaments. Herein, we examined the role of sMyBP-C in adult skeletal muscles using in vivo gene transfer and clustered regularly
Christina Geraldine Kantzer et al.
Journal of neuroscience research, 99(9), 2228-2249 (2021-06-02)
The formation of the cerebellum is highly coordinated to obtain its characteristic morphology and all cerebellar cell types. During mouse postnatal development, cerebellar progenitors with astroglial-like characteristics generate mainly astrocytes and oligodendrocytes. However, a subset of astroglial-like progenitors found in

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