Awareness Technology Chemistry Analyzers - Make the Right Choice [Infographics]December 18th, 2017
QBC STAR™ Dry Hematology System for Faster CBC TestingDecember 15th, 2017
AACC Annual Scientific Meeting and Clinical Lab Expo
Medlab - The World’s Largest Expo
DubaiBooth No.: Z5 G 42
MEDICA 2017 - World Forum for Medicine
Düsseldorf, GermanyBooth No.: 3/D35-2
69th AACC Annual Meeting and Clinical Lab Expo - July 30 - August 3, 2017
SAN DIEGO, CA, USA
Thanks to Block Scientific, I was able to procure the re-certified Bayer DCA 2000+ without hassles and get the lab back in operation. The
device works perfectly and I look forward to doing more business with Block Scientific.
--- Mathew Anderson, New Jersey
The DRG Cytomegalie Virus (CMV) IgM Enzyme Immunoassay Kit provides materials for determination of IgMclass antibodies to Cytomegalie Virus in serum. In the United States, this kit is intended for Research Use Only.
The DRG Cytomegalie Virus (CMV) IgM ELISA Kit is a solid phase enzyme-linked immunosorbent assay (ELISA) Donor samples are diluted with Sample Diluent and additionally incubated with IgG-RF-Sorbent, containing hyperimmune anti-human IgG-class antibody to eliminate competitive inhibition from specific IgG and to remove rheumatoid factors. This pretreatment avoids false negative or false positive results.
Microtiter wells as a solid phase are coated with inactivated Cytomegalie Virus antigen (strain 169). Pretreated donor specimens and ready-for-use controls are pipetted into these wells. During incubation Cytomegalie Virus-specific antibodies of positive specimens and controls are bound to the immobilized antigens.
After a washing step to remove unbound sample and control material horseradish peroxidase conjugated anti-human IgM antibodies are dispensed into the wells. During a second incubation this anti-IgM conjugate binds specificly to IgM antibodies resulting in the formation of enzyme-linked immune complexes.
After a second washing step to remove unbound conjugate the immune complexes formed (in case of positive results) are detected by incubation with TMB substrate and development of a blue color. The blue color turns into yellow by stopping the enzymatic indicator reaction with sulfuric acid.The intensity of this color is directly proportional to the amount of Cytomegalie Virus-specific IgM antibody in the donor specimen. Absorbance at 450 nm is read using an ELISA microtiter plate reader.