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The protein encoded by L1CAM is an axonal glycoprotein belonging to the immunoglobulin supergene family. Additionally we are shipping L1 Cell Adhesion Molecule Kits (37) and L1 Cell Adhesion Molecule Proteins (18) and many more products for this protein.
Showing 10 out of 214 products:
Human Polyclonal L1CAM Primary Antibody for EIA, WB - ABIN951209
Schäfer, Schmitz, Diestel: L1CAM ubiquitination facilitates its lysosomal degradation. in FEBS letters 2010
Show all 4 references for ABIN951209
Human Polyclonal L1CAM Primary Antibody for IF, ELISA - ABIN1532555
Hlavin, Lemmon: Molecular structure and functional testing of human L1CAM: an interspecies comparison. in Genomics 1992
Report high frequency of L1CAM expression in high-risk endometrial cancers associated with mutant p53 (show TP53 Antibodies) expression.
L1CAM is frequently expressed in testicular germ cell tumors but not in normal testis.
Our results suggest that the overexpression of L1CAM may be related to several established markers of poor prognosis in breast cancer patients.
L1-CAM (show CALM1 Antibodies) and N-CAM (show NCAM1 Antibodies): From Adhesion Proteins to Pharmacological Targets
the CE7-epitope of L1-CAM (show CALM1 Antibodies) is a cell adhesion molecule (show MCAM Antibodies) aberrantly expressed in several cancers and may have a role in immunotherapy
novel missense variant in L1CAM was identified in two Caucasian families with mild-moderate intellectual disability without obvious L1 syndrome features
This study identified predicted pathogenic, hemizygous variants on chromosome X in disease genes L1CAM.
Our findings establish Slug (show SNAI2 Antibodies)-induced L1CAM expression as a mediator of a chemoresistant and migratory phenotype in pancreatic adenocarcinoma cells.
the expression level of L1CAM were negatively correlated with miR (show MLXIP Antibodies)-503 levels in osteosarcoma tissues.
L1CAM is expressed in triple-negative breast cancers and is inversely correlated with androgen receptor (show AR Antibodies)
Heterozygous L1CAM-deficient mice express an autism-like phenotype.
tumors in stressed animals demonstrated markedly enhanced expression of VEGFR-2 (show KDR Antibodies) and L1CAM mRNA as well as pERK (show EIF2AK3 Antibodies), MMP-2 (show MMP2 Antibodies) and MMP-9 (show MMP9 Antibodies) protein expression.
Function-triggering antibodies to the adhesion molecule (show NCAM1 Antibodies) L1 enhance recovery after injury of the adult mouse femoral nerve.
We suggest that L1 stimulates neuritogenesis by activating CK2alpha leading to decreased levels of PTEN (show PTEN Antibodies) and p53 (show TP53 Antibodies) via a novel, L1-triggered and CK2alpha-mediated signal transduction pathway.
a positive relationship between L1 and pPKD1 in both cultured cerebellar neurons and human cerebellar tissue, suggesting that L1 functions in the modulation of PKD1 (show PKD1 Antibodies) phosphorylation.
Myelin basic protein (show MBP Antibodies) cleaves cell adhesion molecule (show MCAM Antibodies) L1 and promotes neuritogenesis and cell survival.
These results demonstrate that L1 promotes neuronal differentiation from ESCs (show NR2E3 Antibodies) through the L1-mediated enhancement of FUT9 (show FUT9 Antibodies) and ST3Gal4 (show ST3GAL4 Antibodies) expression.
L1 stimulation triggers sumoylation and cleavage of L1, thus generating the L1-70 fragment which is cleaved by cathepsin E (show CTSE Antibodies)
the neurite outgrowth promoted by Neural Cell Adhesion Molecule L1 was strongly inhibited by siRNA against FGF21 (show FGF21 Antibodies) gene or a treatment of cells with FGFR (show FGFR2 Antibodies) inhibitor
we investigated the role of L1CAM during metastasis formation
The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting of several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause three X-linked neurological syndromes known by the acronym CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of a neuron-specific exon is thought to be functionally relevant.
neural cell adhesion molecule L1
, antigen identified by monoclonal antibody R1
, N-CAM L1
, nerve-growth factor-inducible large external glycoprotein
, neuron-glia cell adhesion molecule (Ng-CAM)
, neuronal-glial cell adhesion molecule