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Prostate Specific Antigen Kit ELISA

Ce kit ELISA Colorimetric est conçu pour la mesure quantitative de Humain Prostate Specific Antigen. Il y a 1 publication disponible.
N° du produit ABIN577067

Aperçu rapide pour Prostate Specific Antigen Kit ELISA (ABIN577067)

Antigène

Voir toutes Prostate Specific Antigen (PSA) Kits ELISA
Prostate Specific Antigen (PSA)

Reactivité

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Humain

Méthode de détection

Colorimetric

Type de méthode

Sandwich ELISA

Application

ELISA
  • Fonction

    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

    Analytical Method

    Quantitative

    Sensibilité

    Estimated to be 1 ng/mL PSA antigen in human serum.

    Ingrédients

    Standards: 1 set/2 vials
  • Plaque

    Pre-coated

    Restrictions

    For Research Use only
  • Agent conservateur

    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." dans: PLoS ONE, Vol. 9, Issue 3, pp. e89772, (2014) (PubMed).

  • Antigène Voir toutes Prostate Specific Antigen (PSA) Kits ELISA

    Prostate Specific Antigen (PSA)

    Sujet

    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

    Système du Complément
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