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Key Documents

MABN323

Sigma-Aldrich

Anti-Ermin Antibody, clone 160

clone 160, from mouse

Synonyme(s) :

Ermin, Juxtanodin

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About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702
Nomenclature NACRES :
NA.41

Source biologique

mouse

Niveau de qualité

Forme d'anticorps

purified immunoglobulin

Type de produit anticorps

primary antibodies

Clone

160, monoclonal

Espèces réactives

mouse, rat

Technique(s)

immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable

Isotype

IgG2aκ

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

wet ice

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

mouse ... Ermn(77767)

Catégories apparentées

Description générale

Ermin is also known as Juxtanodin (JN). Ermin is involved in cytoskeletal rearrangements during myelinogenesis and in the maintenance and stability of the myelin sheath in adults. Ermin is also thought to be important in oligodendroglia maturation, myelin/Ranvier node formation during CNS development, and in the plasticity of related structures in the mature CNS. Ermin is exclusively expressed by oligodendrocytes in the brain and spinal cord, where it appears in the late stages of myelination, and in the mature nerves, it is localized in the outer cytoplasmic lip of the myelin sheath and the paranodal loops.

Immunogène

Recombinant protein corresponding to mouse Ermin.

Application

Anti-Ermin Antibody, clone 160 is a highly specific mouse monoclonal antibody, that targets Ermin & has been tested in western blotting, ICC & IHC.
Immunohistochemistry Analysis: A representative lot from an independent laboratory detected Ermin in mouse wild type sagittal brain sections, and demonstrated a loss of signal in mouse OL-ablated sagittal brain sections (Brockschnieder, D., et al. (2006). J Neurosci. 26(3):737-762).

Immunocytochemistry Analysis: A representative lot from an independent laboratory detected Ermin in certain mouse brain and optic nerve sections (Brockschnieder, D., et al. (2006). J Neurosci. 26(3):737-762).
Research Category
Neuroscience
Research Sub Category
Developmental Neuroscience

Qualité

Evaluated by Western Blotting in mouse brain tissue lysate.

Western Blotting Analysis: 1 µg/mL of this antibody detected Ermin in 10 µg of mouse brain tissue lysate.

Description de la cible

~42 kDa observed. The calculated molecular weight of this protein is 32 kDa; however, it has been observed at ~42 kDa (Brockschnieder, D., et al. (2006). J Neurosci. 26(3):737-76.).

Forme physique

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG2aκ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Stockage et stabilité

Stable for 1 year at 2-8°C from date of receipt.

Remarque sur l'analyse

Control
Mouse brain tissue lysate

Autres remarques

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Clause de non-responsabilité

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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Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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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

Damian Brockschnieder et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 26(3), 757-762 (2006-01-20)
Oligodendrocytes form an insulating multilamellar structure of compact myelin around axons, thereby allowing rapid propagation of action potentials. Despite the considerable clinical importance of myelination, little is known about the molecular mechanisms that enable oligodendrocytes to generate their specialized membrane
Carola I Radulescu et al.
Neurobiology of disease, 135, 104744-104744 (2020-01-14)
Structural and molecular myelination deficits represent early pathological features of Huntington disease (HD). Recent evidence from germ-free (GF) animals suggests a role for microbiota-gut-brain bidirectional communication in the regulation of myelination. In this study, we aimed to investigate the impact

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