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Reelin antibody

RELN Reactivity: Human WB, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7269893
  • Target See all Reelin (RELN) Antibodies
    Reelin (RELN)
    Reactivity
    • 36
    • 24
    • 9
    Human
    Host
    • 35
    • 10
    • 2
    • 1
    Rabbit
    Clonality
    • 29
    • 19
    Polyclonal
    Conjugate
    • 25
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This Reelin antibody is un-conjugated
    Application
    • 29
    • 23
    • 14
    • 9
    • 8
    • 6
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (IHC)
    Purpose
    RELN Rabbit pAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human RELN.
    Isotype
    IgG
    Top Product
    Discover our top product RELN Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000,IHC,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Reelin (RELN)
    Alternative Name
    RELN (RELN Products)
    Synonyms
    LIS2 antibody, PRO1598 antibody, RL antibody, reeler antibody, rl antibody, Reelen antibody, Rl antibody, reln antibody, RELN antibody, MGC172539 antibody, reelin antibody, reelin L homeolog antibody, RELN antibody, Reln antibody, reln antibody, reln.L antibody, LOC579060 antibody
    Background
    This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined. [provided by RefSeq, Jul 2008],ETL7,LIS2,PRO1598,RL,RELN,Cell Biology & Developmental Biology,Cell Adhesion,Neuroscience,Cell Type Marker,RELN
    Gene ID
    5649
    UniProt
    P78509
    Pathways
    Synaptic Membrane
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