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D8168

Sigma-Aldrich

Anti-Dystrophin Antibody

mouse monoclonal, MANDYS8

Sinônimo(s):

Dystrophin Antibody, Dystrophin Antibody - Monoclonal Anti-Dystrophin antibody produced in mouse

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100 μL
R$ 2.504,00
0.2 ML
R$ 3.276,00

R$ 2.504,00


Previsão de entrega em29 de maio de 2025

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100 μL
R$ 2.504,00
0.2 ML
R$ 3.276,00

About This Item

Número MDL:
Código UNSPSC:
12352203
NACRES:
NA.41

R$ 2.504,00


Previsão de entrega em29 de maio de 2025

Um anticorpo recombinante, sem conservantes, está disponível para seu alvo. Tente ZMS1051

Solicite uma grande encomenda

Nome do produto

Monoclonal Anti-Dystrophin antibody produced in mouse, clone MANDYS8, ascites fluid

fonte biológica

mouse

Nível de qualidade

conjugado

unconjugated

forma do anticorpo

ascites fluid

tipo de produto de anticorpo

primary antibodies

clone

MANDYS8, monoclonal

reatividade de espécies

chicken, rat, human, pig, rabbit, mouse

técnica(s)

indirect ELISA: suitable
indirect immunofluorescence: 1:400 using frozen human or animal muscle tissue sections.
microarray: suitable
western blot: suitable

Isotipo

IgG2b

nº de adesão UniProt

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

modificação pós-traducional do alvo

unmodified

Informações sobre genes

human ... DMD(1756)
mouse ... Dmd(13405)
rat ... Dmd(24907)

Descrição geral

Monoclonal Anti-Dystrophin (mouse IgG2b isotype) is derived from the MANDYS8 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse. Dystrophin is a structural protein on the inner face of the membrane, consisting of a 25-repeat, rod-like, triple-helical domain separating an N-terminal actin binding domain from two C-terminal domains, one of which is rich in cysteine.

Imunogênio

recombinant human dystrophin fragment.

Aplicação

Monoclonal Anti-Dystrophin antibody produced in mouse has been used in
  • immunohistochemistry
  • immunofluorescence[1]
  • double immunofluorescence terminal dUTP nick-end labeling (TUNEL)[1]
  • immunoblotting

Monoclonal anti-dystrophin antibody can be used for localization of dystrophin using immunochemical assays like ELISA and immunohistochemistry. The antibody can also be used in immunoblotting for brain dystrophin. Further, it can be used in western blotting and double immunofluorescent labelling (diluted 1: 500) of dystrophin.

Ações bioquímicas/fisiológicas

Dystrophin deficiency is associated with severe Duchenne muscular dystrophy (DMD). Becker muscular dystrophy (BMD) show less pronounced abnormalities of dystrophin protein expression. Since abnormalities in the protein expression occur specifically in patients with these types of muscular dystrophy, dystrophin analysis may be used to distinguish these conditions from other neuromuscular diseases.

Descrição-alvo

The rod domain of the human dystrophin molecule is present in normal muscle tissue and in nearly all Becker muscular dystrophies. It is absent in the cases of Duchenne muscular dystrophies and in the dystrophic mouse (mdx).

Outras notas

This product can be found as purified product that was produced using cell culture hybridoma product.
SAB4200764 Anti-Dystrophin antibody, Mouse monoclonal
clone MANDYS8, purified from hybridoma cell culture

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Effects of long-term resveratrol-induced SIRT1 activation on insulin and apoptotic signalling in aged skeletal muscle
Sin TK, et al.
Acta Diabetologica, 52(6), 1063-1075 (2015)
Myospryn is a calcineurin-interacting protein that negatively modulates slow-fiber-type transformation and skeletal muscle regeneration
Kielbasa OM, et al.
Faseb Journal, 25(7), 2276-2286 (2011)
Rachel Blitzblau et al.
Brain research, 1218, 21-34 (2008-06-06)
Muscular dystrophy patients often show cognitive impairment, in addition to muscle degeneration caused by dystrophin gene defects. The cognitive impairments lead to speculation that the dystrophin protein family may play a key role at neuronal synapses. Dystrophin regulates the stability
The dystrophin complex: structure, function, and implications for therapy
Gao QQ and McNally EM
Comprehensive Physiology, 5(3), 1223-1239 (2011)
Juliette A Strauss et al.
Physiological reports, 4(1) (2016-01-07)
Synaptosomal-associated protein 23 (SNAP23) is a SNARE protein expressed abundantly in human skeletal muscle. Its established role is to mediate insulin-stimulated docking and fusion of glucose transporter 4 (GLUT4) with the plasma membrane. Recent in vitro research has proposed that SNAP23

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