L1CAM Polyclonal Antibody
€0.00
In stock
SKU
E-AB-40465
Catalog Number: E-AB-40465
Isotype: Rabbit IgG
Reactivity: mouse, rat
Applications: IHC
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: mouse, rat
Applications: IHC
Datasheet, Questions? Contact us!
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.
Research Area: Signal Transduction, Neuroscience
Synonyms:
Antigen identified by monoclonal antibody R1, CAML1, CD171, CD171 antigen, HSAS, HSAS1, Hyd, L1 cell adhesion molecule, L1, MASA, L1cam, MIC5, NCAML1, Nerve-growth factor-inducible large external glycoprotein, Neural cell adhesion molecule L1, NILE, OTTHUMP00000025992, S10, SPG1
Immunogen: Recombinant Mouse Neural cell adhesion molecule L1 protein
Swissprot: P11627
Gene ID: 16728
Purification Method: Antigen Affinity Purification
Buffer: PBS with 0.05% Proclin300, 50% glycerol, pH7.3.
Concentration: 1mg/mL
Dilution: IHC 1:200-1:500
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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.
Research Area: Signal Transduction, Neuroscience
Synonyms:
Antigen identified by monoclonal antibody R1, CAML1, CD171, CD171 antigen, HSAS, HSAS1, Hyd, L1 cell adhesion molecule, L1, MASA, L1cam, MIC5, NCAML1, Nerve-growth factor-inducible large external glycoprotein, Neural cell adhesion molecule L1, NILE, OTTHUMP00000025992, S10, SPG1
Immunogen: Recombinant Mouse Neural cell adhesion molecule L1 protein
Swissprot: P11627
Gene ID: 16728
Purification Method: Antigen Affinity Purification
Buffer: PBS with 0.05% Proclin300, 50% glycerol, pH7.3.
Concentration: 1mg/mL
Dilution: IHC 1:200-1:500
Storage:
Store at -20℃. Avoid freeze / thaw cycles.
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