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Prostate Specific Antigen ELISA Kit

PSA Reaktivität: Human Colorimetric Sandwich ELISA
Produktnummer ABIN577067
  • Target Alle Prostate Specific Antigen (PSA) ELISA Kits anzeigen
    Prostate Specific Antigen (PSA)
    Reaktivität
    • 14
    • 9
    • 7
    • 2
    • 2
    • 2
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    • 1
    • 1
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    Human
    Nachweismethode
    Colorimetric
    Methodentyp
    Sandwich ELISA
    Applikation
    ELISA
    Verwendungszweck
    This PSA enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific for PSA. Standards or samples are then added to the microtiter plate wells and PSA, if present, will bind to the antibody pre-coated on the wells. In order to quantify the amount of PSA present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated monoclonal antibody, specific for PSA are added to each well to
    Analytische Methode
    Quantitative
    Sensitivität
    Estimated to be 1 ng/mL PSA antigen in human serum.
    Bestandteile
    Standards: 1 set/2 vials
    Top Product
    Discover our top product PSA ELISA Kit
  • Plattentyp
    Pre-coated
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konservierungsmittel
    Without preservative
  • Petiwala, Berhe, Li, Puthenveetil, Rahman, Nonn, Johnson: "Rosemary (Rosmarinus officinalis) extract modulates CHOP/GADD153 to promote androgen receptor degradation and decreases xenograft tumor growth." in: PLoS ONE, Vol. 9, Issue 3, pp. e89772, (2014) (PubMed).

  • Target Alle Prostate Specific Antigen (PSA) ELISA Kits anzeigen
    Prostate Specific Antigen (PSA)
    Abstract
    PSA Produkte
    Hintergrund
    Hepatitis resulting from infection with viruses other than Hepatitis A Virus (HAV) and Hepatitis B (HBV) virus was previously referred to as non-A, non-B hepatitis. The first characterised non-A, non-B hepatitis agent was that responsible for parentally transmitted non-A, non-B hepatitis, or what is now called Hepatitis C Virus. This was followed by the cloning of a portion of the fecal-orally-transmitted agent, the Hepatitis E Virus (HEV). Hepatitis E Virus has been referred to as enterically transmitted non-A, non-B hepatitis. Epidemics of enterically transmitted Hepatitis E Virus have been recognised worldwide but occur principally in developing countries. They have been reported in Southeast Asia, central Asia, Africa, Mexico, and Central America. In these areas, contaminated water has been implicated as the principal vehicle of virus transmission. Although HEV and HAV are transmitted in a similar manner, there are major differences in the clinical, pathological, and epidemiological courses of these two viruses. In particular, the mortality rate for HEV infection is 1 to 2%, or approximately 1-fold greater than that seen for HAV. Infection with HEV is particularly fatal for pregnant women, for whom the mortality rate can be as high as 1 to 2%
    Pathways
    Komplementsystem
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