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L1CAM antibody (PE)

The PE-conjugated Rabbit Monoclonal anti-L1CAM antibody (Clone DM155) (ABIN7867348) specifically detects L1CAM in FACS. The antibody is reactive with Human samples.
Catalog No. ABIN7867348
$927.69
Plus shipping costs $50.00
100 tests
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for L1CAM antibody (PE) (ABIN7867348)

Target

See all L1CAM Antibodies
L1CAM (L1 Cell Adhesion Molecule (L1CAM))

Reactivity

  • 159
  • 44
  • 40
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 116
  • 48
  • 2
  • 1
Rabbit

Clonality

  • 87
  • 79
  • 1
Monoclonal

Conjugate

  • 100
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  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This L1CAM antibody is conjugated to PE

Application

  • 89
  • 56
  • 50
  • 49
  • 25
  • 15
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  • 13
  • 10
  • 5
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  • 1
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Flow Cytometry (FACS)

Clone

DM155
  • Purpose

    PE-conjugated Anti-CD171 antibody(DM155), Rabbit mAb

    Purification

    Purified from cell culture supernatant by affinity chromatography

    Isotype

    IgG
  • Application Notes

    Flow Cyt 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid PBS with 0.05 %  Proclin300, 1 % BSA

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Storage Comment

    Store at 2°C-8°C for 6 months

    Expiry Date

    6 months
  • Target

    L1CAM (L1 Cell Adhesion Molecule (L1CAM))

    Alternative Name

    CD171

    Background

    Synonyms: CAML1, CD171, HSAS, HSAS1, MASA, MIC5, N-CAM-L1, N-CAML1, NCAM-L1, S10, SPG1

    Target 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.

    UniProt

    P32004

    Pathways

    Synaptic Membrane
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