This product is quite robust and versatile. It has been found suitable for use in a number of applications - flow cytometry, immunocytochemistry, immunohistochemistry, immunoprecipitation, microarray and western blot - however it has not tested for use in electron microscopy. It would be up to the end user to determine suitability. Should this be of interest, please see the link below to learn more about the Antibody Guarantee program:
https://www.sigmaaldrich.com/US/en/technical-documents/technical-article/protein-biology/immunohistochemistry/bioguarantee-antibodies
L4543
Anti-L1CAM antibody, Mouse monoclonal
clone UJ127.11, purified from hybridoma cell culture
Synonyme(s) :
L1CAM Antibody - Anti-L1CAM antibody, Mouse monoclonal, L1Cam Antibody, Anti-CAML1, Anti-L1 Cell Adhesion Molecule, Anti-MIC5, Anti-Neural Cell Adhesion Molecule L1
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About This Item
Le tarif et la disponibilité ne sont pas disponibles actuellement.
Produits recommandés
Source biologique
mouse
Niveau de qualité
Conjugué
unconjugated
Forme d'anticorps
purified immunoglobulin
Type de produit anticorps
primary antibodies
Clone
UJ127.11, monoclonal
Forme
buffered aqueous solution
Poids mol.
antigen 220-240 kDa
Espèces réactives
human
Conditionnement
antibody small pack of 25 μL
Concentration
~2 mg/mL
Technique(s)
flow cytometry: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
microarray: suitable
western blot: 0.25-0.5 μg/mL using cell extracts of G361 cells (human melanoma)
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
human ... L1CAM(3897)
Description générale
Anti-L1CAM antibody, Mouse monoclonal (mouse IgG1 isotype) is derived from the hybridoma UJ127.11 produced by the fusion of mouse myeloma cells (P3- X63-Ag8-653 cells) and splenocytes from mice immunized with human fetal brain. L1 cell adhesion molecule (L1CAM) protein belongs to the family of cell adhesion molecules (CAM).
The gene L1CAM (L1 cell adhesion molecule) encodes a member of the immunoglobulin supergene family. The encoded protein contains a cytoplasmic intracellular domain, one single-pass transmembrane region and an extracellular domain containing six immunoglobulin- (Ig) and five fibronectin (Fn) III-like motifs. The gene is mapped to human chromosome Xq28. It contains 29 exons that encode a protein of 1257 amino acids containing a 19 amino acid signal peptide and a functional L1 protein of 1238 amino acids. It is mainly expressed in the nervous system.
Immunogène
L1CAM from human fetal brain.
Application
Anti-L1CAM antibody has been used in immunohistochemistry.[1]
Anti-L1CAM antibody, Mouse monoclonal has been used for:
- immunohistochemistry
- immunoprecipitation
- immunoblotting
- immunocytochemistry
- flow cytometry
Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunohistochemistry (1 paper)
Western Blotting (1 paper)
Immunohistochemistry (1 paper)
Western Blotting (1 paper)
Actions biochimiques/physiologiques
L1 cell adhesion molecule (L1CAM) is critical for central nervous system (CNS) development in humans. This protein is responsible for many activities among them: neurite outgrowth, adhesion, fasciculation and myelination. These activities are mediated by the interaction of L1CAM with various members of the CAM protein family, extracellular matrix molecules and signaling receptors, through interactions that involve the extracellular domain of L1CAM. Mutations in the L1CAM gene may be linked to several brain disorders such as type 1 X-linked spastic paraplegia (SPG1), MASA syndrome and ACC (agenesis of corpus callosum).
The gene L1CAM (L1 cell adhesion molecule) encodes a glycoprotein that functions in axon growth during development and axon bundling. It interacts with Schwann cells and axons, and mediates neuronal cell migration, and neuronal cell survival. Overexpression of this protein is associated with tumor progression. It has been found to mediate therapeutic resistance in ovarian and pancreatic cancer cells.
Forme physique
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
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)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
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Les clients ont également consulté
Luiz M Nova-Camacho et al.
Archives of pathology & laboratory medicine (2022-09-29)
In 2019, papillary renal neoplasm with reverse polarity (PRNRP) was defined as a new neoplasm because it has a predominately tubulopapillary pattern lined by a single layer of cuboidal and eosinophilic cells with apically located round nuclei. Immunohistochemically, this neoplasm
Meredith Stevers et al.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 32(1), 88-99 (2018-09-02)
Well-differentiated papillary mesothelioma is an uncommon mesothelial neoplasm that most frequently arises in the peritoneal cavity of women of reproductive age. Whereas malignant mesothelioma is an aggressive tumor associated with poor outcome, well-differentiated papillary mesothelioma typically exhibits indolent behavior. However
Dario Van Meenen et al.
International journal of molecular sciences, 23(20) (2022-10-28)
A disintegrin and metalloproteinase (ADAM) family proteins, acting as sheddases, are important factors in a number of pathologies, including cancer, and have been suggested as promising therapeutic targets. The study presented focuses on the involvement of ADAM10 and ADAM17 in
L1 cell adhesion molecule (L1CAM) in invasive tumors
Raveh S, et al.
Cancer letters, 282(2), 137-145 (2009)
Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): mutations in the L1CAM gene
Weller S and Gartner J
Human Mutation, 18(1), 1-12 (2001)
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I can use this anthibody for electron microscopy? Or could you advise me how to try L1CAM in electron microscopy?
1 answer-
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