Search Results - "Roman, M.G"

  • Showing 1 - 4 results of 4
Refine Results
  1. 1

    Shelf life and Clostridium botulinum toxin development during storage of modified atmosphere-packaged fresh catfish fillets by Reddy, N.R. (FDA, Summit-Argo, IL.), Roman, M.G, Villanueva, M, Solomon, H.M, Kautter, D.A, Rhodenhamel, E.J

    Published in Journal of food science (01-07-1997)
    “…Shelf life (onset of sensory spoilage) and potential for toxin production by Clostridium botulinum type E in retail type packages of fresh catfish fillets in…”
    Get full text
    Journal Article
  2. 2

    Toxin development by Clostridium botulinum in modified atmosphere-packaged fresh tilapia fillets during storage by REDDY, N.R., PARADIS, A., ROMAN, M.G., SOLOMON, H.M., RHODEHAMEL, E.J.

    Published in Journal of food science (01-05-1996)
    “…Potential for toxin development by Clostridium botulinum type E was investigated in retail-type packages of fresh tilapia fillets packaged in high barrier film…”
    Get full text
    Journal Article
  3. 3

    Sensitive enzyme-linked immunosorbent assay for detection of Clostridium botulinum neurotoxins A, B, and E, using signal amplification via enzyme-linked coagulation assay by Doellgast, G.J, Triscott, M.X, Beard, G.A, Bottoms, J.D, Cheng, T, Roh, B.H, Roman, M.G, Hall, P.A, Brown, J.E

    Published in Journal of Clinical Microbiology (01-09-1993)
    “…A new immunoassay amplification method has been applied to the measurement of toxins A, B, and E from Clostridium botulinum. The technique is a modified…”
    Get full text
    Journal Article
  4. 4

    Enzyme-linked immunosorbent assay and enzyme-linked coagulation assay for detection of Clostridium botulinum neurotoxins A, B, and E and solution-phase complexes with dual-label antibodies by Doellgast, G J, Beard, G A, Bottoms, J D, Cheng, T, Roh, B H, Roman, M G, Hall, P A, Triscott, M X

    Published in Journal of Clinical Microbiology (1994)
    “…The measurement of toxins A, B, and E from Clostridium botulinum was accomplished by use of a modified sandwich enzyme-linked immunosorbent assay (ELISA)…”
    Get full text
    Journal Article