Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

DISC1 Protein (Transcript Variant L) (Myc-DYKDDDDK Tag)

DISC1 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2719502
  • Target See all DISC1 Proteins
    DISC1 (Disrupted in Schizophrenia 1 (DISC1))
    Protein Type
    Recombinant
    Protein Characteristics
    Transcript Variant L
    Origin
    • 3
    • 2
    • 2
    Human
    Source
    • 5
    • 2
    HEK-293 Cells
    Purification tag / Conjugate
    This DISC1 protein is labelled with Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human DISC1 (transcript variant L) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product DISC1 Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    DISC1 (Disrupted in Schizophrenia 1 (DISC1))
    Alternative Name
    Disc1 (DISC1 Products)
    Synonyms
    DISC1 Protein, C1orf136 Protein, SCZD9 Protein, disrupted in schizophrenia 1 Protein, disrupted in schizophrenia 1 protein Protein, disc1 Protein, DISC1 Protein, LOC100580606 Protein, Disc1 Protein
    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(111)(q42.1q14.3) translocation which segregates with schizophrenia and related psychiatric disorders in a large Scottish family. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
    Molecular Weight
    93.4 kDa
    NCBI Accession
    NP_061132
    Pathways
    Regulation of Cell Size
You are here:
Support