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C9672

Sigma-Aldrich

Monoclonal Anti-Neural Cell Adhesion Molecule antibody produced in mouse

clone NCAM-0B11, ascites fluid

Synonyme(s) :

Anti-CD56-CY, Anti-NCAM

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

mouse

Niveau de qualité

Conjugué

unconjugated

Forme d'anticorps

ascites fluid

Type de produit anticorps

primary antibodies

Clone

NCAM-0B11, monoclonal

Poids mol.

antigen 140-180 kDa

Contient

15 mM sodium azide

Espèces réactives

rat, human

Technique(s)

immunocytochemistry: suitable using cells and tissues
western blot: 1:100 using a freshly prepared extract from newborn and adult rat brain, or rat cerebral cortex extract

Isotype

IgG1

Numéro d'accès UniProt

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

Description générale

Monoclonal Anti-N-CAM (mouse IgG1 isotype) is derived from the hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse. Neural cell adhesion molecule (N-CAM), the best characterized CAM, exists in adult brain. It belongs to the family of sialoglycoproteins, which arise from alternative splicing of mRNA transcribed from a single gene. Immunocytochemical data indicate that in the adult, N-CAM is expressed mainly in cells of the nervous system. There are indications that N-CAM may also be expressed by non-neural cells in the adult, as it has been found in studies of various embryonic developmental stages.
Mouse monoclonal clone NCAM-0B11 anti-Neural Cell Adhesion Molecule antibody localizes the high molecular weight isoform of N-CAM (neural cell adhesion molecule) in human and several other mammalian species. The antibody shows a strong reaction to N-CAM A/N-CAM 180, however it also recognizes N-CAM B/N-CAM 140. In an immunoblot, the product reacts with polysialated N-CAM in embryonic material. Breakdown products of N-CAM may be stained; they appear as bands lower than 100 kD on the immunoblot.

Immunogène

growth cone enriched plasma membrane fraction from E17 rat forebrain.

Application

Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunofluorescence (1 paper)
Immunohistochemistry (3 papers)
Monoclonal Anti-Neural Cell Adhesion Molecule antibody produced in mouse has been used in:
  • Immunofluorescence
  • Immunohistochemistry
  • Immunoblotting

Actions biochimiques/physiologiques

Neural cell adhesion molecule (N-CAM) are believed to be involved in cell-cell interactions and probably play an important role in embryogenesis and development.

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

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

nwg

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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Les clients ont également consulté

Neural cell adhesion molecule (NCAM) isoform expression is associated with neuroblastoma differentiation status
Winter C, et al.
Pediatric Blood & Cancer, 51(1), 10-16 (2008)
The ubiquitous neural cell adhesion molecule (N-CAM)
Weledji EP and Assob JC
Annals of medicine and surgery, 3(3), 77-81 (2014)
Nephron Progenitor But Not Stromal Progenitor Cells Give Rise to Wilms Tumors in Mouse Models with
Huang L, et al.
Neoplasia, 18(2), 71-81 (2016)
Kif3a controls murine nephron number via GLI3 repressor, cell survival, and gene expression in a lineage-specific manner
Chi L et al.
Testing, 8(6), e65448-e65448 (2013)
Expression and localization of neural cell adhesion molecule and polysialic acid during chick corneal development
Mao X, et al.
Investigative Ophthalmology & Visual Science, 53(3), 1234-1243 (2012)

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