Tests from Roche, Siemens and Becton Dickinson Get FDA Approval in MarchApril 20th, 2018
Eppendorf Starts Off 2018 Introducing Two New Benchtop CentrifugesApril 18th, 2018
MEDICA 2017 - World Forum for Medicine
Düsseldorf, GermanyBooth No.: 3/D35-2
AACC Annual Scientific Meeting and Clinical Lab Expo
ChicagoBooth No.: 3849
Medlab - The World’s Largest Expo
DubaiBooth No.: Z5 G 42
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 Herpes Simplex Virus Type 1 + 2 IgM Enzyme Immunoassay Kit is for determination of IgM-class antibodies to Herpes Simplex Virus Type 1 + 2 in human serum. This kit is intended for Research Use Only.
The DRG Herpes Simplex Virus Type 1 + 2 IgM ELISA Kit is a solid phase enzyme-linked immunosorbent assay (ELISA) Samples are diluted with Sample Diluent and additionally incubated with IgG-RF-Sorbent, containing hyper-immune 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 Herpes Simplex Virus Type 1 + 2 antigen.
Pretreated specimens and ready-for-use controls are pipetted into these wells. During incubation Herpes Simplex Virus Type 1 + 2-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 specifically 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 Herpes Simplex Virus Type 1 + 2-specific IgM antibody in the specimen. Absorbance at 450 nm is read using an ELISA microtiter plate reader.