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SV40 Large T and Small Ts antibody

Reactivity: Virus IF, IP, IHC, WB Host: Mouse Monoclonal PAb 108 unconjugated
Catalog No. ABIN967412
  • Target
    SV40 Large T and Small Ts
    Reactivity
    Virus
    Host
    Mouse
    Clonality
    Monoclonal
    Application
    Immunofluorescence (IF), Immunoprecipitation (IP), Immunohistochemistry (IHC), Western Blotting (WB)
    Brand
    BD Pharmingen™
    Characteristics
    1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
    2. Please refer to us for technical protocols.
    3. Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
    Purification
    The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
    Immunogen
    SV40-transformed BALB/c mouse cells
    Clone
    PAb 108
    Isotype
    IgG2a
  • Application Notes
    By SDS-PAGE, T-ag migrates at 90-100 kDa and t-ag at 15-20 kDa. COS-7 kidney monkey cells (ATCC CRL 1651), other established SV40-transformed cell lines, SV40-virus infected cells, or cells transfected with SV40 DNA should be used as a positive control. Other applications include immunoprecipitation, Western blot analysis, immunofluorescence microscopy, immunohistochemical staining of acetone-fixed, tissue culture cells (cytospin) and SV40 origin DNA binding assays, although this application has not been. The biotin-conjugated antibody, ABIN967413 is recommended for cytospin staining and IHC applications.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.5 mg/mL
    Buffer
    Aqueous buffered solution containing ≤0.09 % 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
    Storage Comment
    Store undiluted at 4°C.
  • Gurney, Tamowski, Deppert: "Antigenic binding sites of monoclonal antibodies specific for simian virus 40 large T antigen." in: Journal of virology, Vol. 57, Issue 3, pp. 1168-72, (1986) (PubMed).

    Hinzpeter, Fanning, Deppert: "A new sensitive target-bound DNA binding assay for SV40 large T antigen." in: Virology, Vol. 148, Issue 1, pp. 159-67, (1986) (PubMed).

    Mellor, Smith: "Characterization of the amino-terminal tryptic peptide of simian virus 40 small-t and large-T antigens." in: Journal of virology, Vol. 28, Issue 3, pp. 992-6, (1979) (PubMed).

  • Target
    SV40 Large T and Small Ts
    Target Type
    Viral Protein
    Background
    Simian virus 40 (SV40) is a small DNA virus encoded by 5.2 kb of double-stranded DNA. SV40 large T-antigen (T-ag) is a multifunctional ~85 kDa phosphoprotein, which is the sole viral protein required for SV40 replication. All other factors are provided by the infected host cell. In addition to its role in SV40 DNA replication, T-ag also causes transformation of susceptible cell lines. Studies of various mutant T-ag proteins have shown that the replication and transformation fractions of T-ag can be separated. The multifunctional nature of this protein has resulted in its use as a model system in a wide variety of disciplines. T-ag exercises negative regulation on the transcription of SV40 early mRNA by feedback inhibition and exerts positive regulation on transcription from the late promoter. In addition to transcriptional regulation, T-ag is involved in viral DNA replication. Specific biochemical functions required for DNA synthesis that are inherent to the T-ag include high-affinity binding to sites within the viral origin of DNA synthesis, ATPase, and helicase activities. Other functions attributed to T-ag include cellular transformation, induction of cellular DNA synthesis, induction of rRNA synthesis, and provision of a host-range function for viral replication. However, functions of T-ag are influenced by a wide range of post-translational modifications including phosphorylation, glycosylation, acetylation, acylation, and adenylation. T-ag exists in monomeric as well as polymeric forms, and associates with the tumor suppressor proteins p53 and retinoblastoma protein (Rb). Most of T-ag is transported to the nucleus, while a small fraction is localized at the cell surface. Small t-Ag is a polypeptide which shares 82 N-terminal amino acids with large T antigen and has a unique C-terminal region. Clone PAb 108 recognizes an N-terminal epitope within the first 82 amino acids of T-ag and small t antigen (t-ag). B4 SV40-transformed BALB/c mouse fibroblasts were used as immunogen. PAb 108 was originally produced and characterized as part of a panel of antibodies designated PAb 102-117.
    Molecular Weight
    90-100 kDa
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