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DISC1 antibody

DISC1 Reactivity: Human WB, IF Host: Rabbit Monoclonal unconjugated
Catalog No. ABIN7266799
  • Target See all DISC1 Antibodies
    DISC1 (Disrupted in Schizophrenia 1 (DISC1))
    Reactivity
    • 70
    • 25
    • 14
    • 1
    Human
    Host
    • 69
    • 4
    • 1
    • 1
    Rabbit
    Clonality
    • 72
    • 5
    Monoclonal
    Conjugate
    • 42
    • 6
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This DISC1 antibody is un-conjugated
    Application
    • 47
    • 31
    • 26
    • 14
    • 14
    • 11
    • 11
    • 7
    • 6
    • 5
    • 5
    • 3
    • 1
    Western Blotting (WB), Immunofluorescence (IF)
    Purpose
    DISC1 Rabbit mAb
    Cross-Reactivity
    Human, Mouse, Rat
    Characteristics
    Monoclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    A synthesized peptide derived from human DISC1
    Isotype
    IgG
    Top Product
    Discover our top product DISC1 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000,IF,1:50 - 1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,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
    DISC1 (Disrupted in Schizophrenia 1 (DISC1))
    Alternative Name
    DISC1 (DISC1 Products)
    Synonyms
    DISC1 antibody, C1orf136 antibody, SCZD9 antibody, disrupted in schizophrenia 1 antibody, disrupted in schizophrenia 1 protein antibody, disc1 antibody, DISC1 antibody, LOC100580606 antibody, Disc1 antibody
    Background
    This gene encodes a protein with multiple coiled coil motifs which is located in the nucleus, cytoplasm and mitochondria. The protein is involved in neurite outgrowth and cortical development through its interaction with other proteins. This gene is disrupted in a t(1,11)(q42.1,q14.3) translocation which segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008],C1orf136, SCZD9,Cell Biology & Developmental Biology,Cell Cycle,Cell Cycle_Centrosome,Epigenetics & Nuclear Signaling,Neurodegenerative Diseases,Neurodegenerative Diseases_Amyloid Plaque and Neurofibrillary Tangle Formation in Alzheimers Disease,Neuroscience,DISC1
    Molecular Weight
    100kDa
    Gene ID
    27185
    UniProt
    Q9NRI5
    Pathways
    Regulation of Cell Size
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