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Merck

D8281

Anti-Desmin antibody produced in rabbit

whole antiserum

Synonyme(s) :

Anti-Desmin, Desmin Detection Antibody, Rabbit Anti-Desmin

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A propos de cet article

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
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Nom du produit

Anti-Desmin antibody produced in rabbit, whole antiserum

biological source

rabbit

conjugate

unconjugated

antibody form

whole antiserum

antibody product type

primary antibodies

clone

polyclonal

contains

15 mM sodium azide

species reactivity

chicken, bovine, human, mouse

enhanced validation

independent
Learn more about Antibody Enhanced Validation

technique(s)

indirect immunofluorescence: 1:20 using cultured cells
indirect immunofluorescence: 1:20 using human skeletal muscle sections
western blot: 1:100 using animal or human skeletal muscle.

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Gene Information

human ... DES(1674)
mouse ... Des(13346)

Catégories apparentées

Application

Anti-Desmin antibody produced in rabbit has been used in:
  • immunohistochemistry of zebrafish intestines sections
  • immunodetection in fish embryo samples
  • immunolabeling of myofibers

Anti-desmin antibody can be used in immunocytochemistry and western immunoblotting. It can also be used in indirect immunofluorescence.

Biochem/physiol Actions

Desmin plays a crucial role in providing mechanical strength to muscle tissues. Mutations in desmin gene contributes to imbalance in skeletal proteins, resulting in desminopathies. Missense mutations in desmin gene leads to hypertrophic cardiomyopathy and systemic myopathy. Mutations in desmin gene impairs the stability of intermediary filaments in cardiomyocytes, contributing to pathophysiology of cardiac diseases.

Disclaimer

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.

General description

Desmin is an intermediate filament protein found mainly in skeletal, cardiac, and smooth muscle cells. It acts as a marker for tumor origin. It also facilitates mechanical support for muscles, mitochondrial localization, myofibrillogenesis, gene expression regulation, and intracellular signalling. Anti-desmin antibody can be used for immunocytochemical localization of intermediate filaments in all types of muscle cells. It can also be used to stain a wide desmin band of 50,000 to 55,000 molecular weight using immunoblotting assays. Rabbit anti-desmin antibody reacts specifically with desmin in bovine, mouse, chicken and human.
Desmin is mapped to human chromosome 2q35. The desmin protein comprises of a head domain, four α-helical segments, three non-helical rod segments and a tail domain. It exists as dimer and tetramer assemblies. In smooth and striated muscles, desmin is localized in the periphery of Z-disk.

Immunogen

desmin from chicken gizzard

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Classe de stockage

10 - Combustible liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Aberrant Mitochondrial Fission Is Maladaptive in Desmin Mutation-Induced Cardiac Proteotoxicity.
Alam S, et al.
Journal of the American Heart Association, 7(14), e009289-e009289 (2018)
Functional characterization of the novel DES mutation p. L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect.
Brodehl A, et al.
Journal of Molecular and Cellular Cardiology, 91(1), 207-214 (2016)
Imbalances in protein homeostasis caused by mutant desmin.
Winter L, et al.
Neuropathology and Applied Neurobiology (2018)
Myogenin promotes myocyte fusion to balance fibre number and size.
Ganassi M, et al.
Nature Communications, 9(1), 4232-4232 (2018)
Phenotypic expression of a novel desmin gene mutation: hypertrophic cardiomyopathy followed by systemic myopathy.
Harada H, et al.
Journal of Human Genetics, 63(2), 249-249 (2018)

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