L1CAM anticorps
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- Antigène Voir toutes L1CAM Anticorps
- L1CAM (L1 Cell Adhesion Molecule (L1CAM))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp L1CAM est non-conjugé
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Application
- Western Blotting (WB)
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human L1CAM
- Isotype
- IgG
- Top Product
- Discover our top product L1CAM Anticorps primaire
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- Indications d'application
- WB 1:500 - 1:2000
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- L1CAM (L1 Cell Adhesion Molecule (L1CAM))
- Autre désignation
- L1CAM (L1CAM Produits)
- Synonymes
- anticorps l1cam-a, anticorps CAML1, anticorps CD171, anticorps HSAS, anticorps HSAS1, anticorps MASA, anticorps MIC5, anticorps N-CAM-L1, anticorps N-CAML1, anticorps NCAM-L1, anticorps S10, anticorps SPG1, anticorps L1, anticorps Hsas, anticorps Hyd, anticorps NCAML1, anticorps L1 cell adhesion molecule S homeolog, anticorps L1 cell adhesion molecule, anticorps l1cam.S, anticorps L1CAM, anticorps L1cam
- Sujet
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Synonyms: Antigen identified by monoclonal R1,CAML1,CD171,CD171 antigen,HSAS,HSAS1,Hyd,L1,L1 cell adhesion molecule,L1-NCAM,L1cam,L1CAM,MASA,MIC5,N CAML1,N-CAM-L1,NCAM-L1,NCAML1,Nerve-growth factor-inducible large external glycoprotein,Neural cell adhesion molecule L1,NILE,OTTHUMP00000025992,S10,SPG1
Background: 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 X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing of this gene results in multiple transcript variants, some of which include an alternate exon that is considered to be specific to neurons.
- Poids moléculaire
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Observed_MW: 200kDa
Calculated_MW: 138kDa/139kDa/140kDa
- ID gène
- 3897
- UniProt
- P32004
- Pathways
- Synaptic Membrane
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