Recombinant CD171/N-CAML1/L1CAM Monoclonal Antibody (AN300178P)
For research use only.
| Verified Samples |
Verified Samples in IHC: Human appendix Verified Samples in IF: Hela Verified Samples in FCM: HeLa |
| Dilution | IHC-P 1:100-1:500, ICC/IF 1:20-1:100, FCM 1:25-1:100, |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human |
| Applications | IHC-P, FCM, ICC/IF |
| Clonality | Rabbit Monoclonal |
| Immunogen | Recombinant Human CD171 / N-CAML1 / L1CAM protein |
| Abbre | L1CAM |
| Synonyms | MIC, SPG, CAML, N-CAML, NCAM-L, N-CAM-L, L1CAM, CAML1, CD171, HSAS, HSAS1, MASA, MIC5, N-CAM-L1, N-CAML1, NCAM-L1, S10, SPG1, N-CAM L1, L1 antigen, CAML1, CD171, HSAS, HSAS1, L1cam, MASA, MIC5, S10, SPG1, Antigen identified by monoclonal antibody R1, Antigen identified by monoclonal R1, CD171 antigen, Hyd, L1 cell adhesion molecule, L1-NCAM, N CAML1, NCAML1, Nerve-growth factor-inducible large external glycoprotein, Neural cell adhesion molecule L1, NILE, OTTHUMP00000025992 |
| Swissprot | |
| Cellular Localization | Cell membrane, Cell projection, Growth cone, Axon, Dendrite. |
| Concentration | 1 mg/mL |
| Buffer | 0.2 μm filtered solution in PBS |
| Purification Method | Protein A |
| Research Areas | Signal Transduction, Neuroscience |
| Clone No. | 8B9 |
| Conjugation | Unconjugated |
| Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
| Shipping | Ice bag |
| 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. |
Other Clones
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Other Formats
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Unconjugated
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