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BAT1 antibody (C-Term)

DDX39 Reactivity: Human WB, FACS, IHC (p) Host: Rabbit Polyclonal RB22515 unconjugated
Catalog No. ABIN1881102
  • Target See all BAT1 (DDX39) Antibodies
    BAT1 (DDX39) (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39 (DDX39))
    Binding Specificity
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 351-380, C-Term
    Reactivity
    • 11
    • 5
    • 4
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 7
    • 4
    Rabbit
    Clonality
    • 8
    • 3
    Polyclonal
    Conjugate
    • 10
    • 1
    This BAT1 antibody is un-conjugated
    Application
    • 10
    • 5
    • 2
    • 2
    • 2
    • 2
    • 1
    Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Predicted Reactivity
    M, Rat, B, C, D, Pig
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This BAT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 351-380 amino acids from the C-terminal region of human BAT1.
    Clone
    RB22515
    Isotype
    Ig Fraction
  • Application Notes
    WB: 1:1000. WB: 1:1000. IHC-P: 1:10~50. FC: 1:10~50
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Expiry Date
    6 months
  • Choudhary, Kumar, Gnad, Nielsen, Rehman, Walther, Olsen, Mann: "Lysine acetylation targets protein complexes and co-regulates major cellular functions." in: Science (New York, N.Y.), Vol. 325, Issue 5942, pp. 834-40, (2009) (PubMed).

  • Target
    BAT1 (DDX39) (DEAD (Asp-Glu-Ala-Asp) Box Polypeptide 39 (DDX39))
    Alternative Name
    BAT1 (DDX39 Products)
    Synonyms
    dxd39 antibody, MGC53693 antibody, MGC130793 antibody, ddx39 antibody, MGC53944 antibody, DDX39 antibody, 2610307C23Rik antibody, BAT1 antibody, DDXL antibody, Ddx39a antibody, URH49 antibody, bat1 antibody, uap56 antibody, D6S81E antibody, UAP56 antibody, Bat1 antibody, Bat1a antibody, p47 antibody, DEAD-box helicase 39A S homeolog antibody, nuclear RNA helicase antibody, DExD-box helicase 39A antibody, DEAD-box helicase 39A antibody, ATP-dependent RNA helicase DDX39 antibody, ATP-dependent RNA helicase DDX39A antibody, DEAD (Asp-Glu-Ala-Asp) box polypeptide 39b antibody, DEAD (Asp-Glu-Ala-Asp) box polypeptide 39 antibody, DEAD-box helicase 39B L homeolog antibody, DExD-box helicase 39B antibody, ddx39a.S antibody, ddx39 antibody, DDX39A antibody, ddx39a antibody, LOC100084960 antibody, ddx39b antibody, Ddx39 antibody, ddx39b.L antibody, DDX39B antibody, Ddx39b antibody
    Background
    Component of the THO subcomplex of the TREX complex. The TREX complex specifically associates with spliced mRNA and not with unspliced pre-mRNA. It is recruited to spliced mRNAs by a transcription-independent mechanism. Binds to mRNA upstream of the exon-junction complex (EJC) and is recruited in a splicing-and cap-dependent manner to a region near the 5' end of the mRNA where it functions in mRNA export. The recruitment occurs via an interaction between THOC4 and the cap-binding protein NCBP1. UAP56 functions as a bridge between THOC4 and the THO complex. The TREX complex is essential for the export of Kaposi's sarcoma-associated herpesvirus (KSHV) intronless mRNAs and infectious virus production. The recruitment of the TREX complex to the intronless viral mRNA occurs via an interaction between KSHV ORF57 protein and THOC4. Splice factor that is required for the first ATP-dependent step in spliceosome assembly and for the interaction of U2 snRNP with the branchpoint. It has both RNA-stimulated ATP binding/hydrolysis activity and ATP-dependent RNA unwinding activity. Even with the stimulation of RNA, the ATPase activity is weak. It can only hydrolyze ATP but not other NTPs. The RNA stimulation of ATPase activity does not have a strong preference for the sequence and length of the RNA. However, ssRNA stimulates the ATPase activity much more strongly than dsRNA. It can unwind 5' or 3' overhangs or blunt end RNA duplexes in vitro. The ATPase and helicase activities are not influenced by U2AF2 and THOC4.
    Molecular Weight
    48991
    NCBI Accession
    NP_004631, NP_542165
    UniProt
    Q13838
    Pathways
    Ribonucleoprotein Complex Subunit Organization
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