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Description
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. [provided by RefSeq
Specifications
Specifications
| Antigen | L1CAM |
| Applications | ELISA, Western Blot |
| Classification | Monoclonal |
| Clone | 3B10 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a partial recombinant L1CAM. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | L1CAM |
| Gene Accession No. | NM_000425 |
| Gene Alias | CAML1/CD171/HSAS/HSAS1/MASA/MIC5/N-CAML1/S10/SPG1 |
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