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A NEW PEPTIDE-BASED MAGNETIC PARTICLE EIA for individual detection of IgG
antibodies against recombinant p24 (CORE), synthetic peptides to gp41 (TM1), synthetic
peptides to gp120/recombinant gp41 (ENV) and synthetic peptides to gp36 (TM2)
Reagents:
Everything needed for performing the assay is included in the kit. The reagents are
supplied “ready to use” in droppers. Very robust reagents. 12 months shelf life.
No reduction in shelf life after opening the kit. No temperature critical steps
Testing station:
The testing station to be used with the Bionor™ HIV-1&2 Confirmatory Test, consists
of a
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Company:
Date:
November 10, 2008
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Rapid, Visual Chromatographic Assqy for Detection of HIV Antibodies
- For Field & Healthcare Professional Use
- Sensitivity more than 99 per cent
- Specificity more than 99 per cent
- Panel Confirmation: 100 per cent
- Detect HIV 1&2 and HIV 1 subtype "O"
- Less than 1 minute hands-on time
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Company:
Date:
March 03, 2009
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HIV Confirmatory Tests
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Company:
Date:
November 10, 2008
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Sensitive and more specific than western blot
bullet 90 Minute Procedure - comparison chart to western blot
bullet FDA Cleared for use as "primary" HIV-1 Confirmation
bullet Cost Effective
bullet Easy to learn and use
bullet Serum, Plasma and Dry Blood Spot Procedures
bullet Over 10 Years of Uninterrupted Supply!
bullet Used by Public Health, Blood Bank, Plasma, Hospital and Private Labs
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Company:
Date:
November 10, 2008
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The Genetic Systems™ HIV-1 Western Blot is a supplemental,
more specific test for the detection of antibodies to
HIV-1. The solid phase antigens are derived
from LAV strain of HIV-1 grown in the CEM
cell line. Use of the CEM cell line, which is
devoid of HLA Class ll antigens, helps
reduce cross reactivity to cell related, nonviral
bands. In addition, the Genetic
Systems HIV-1 Western Blot offers a
same-day procedure for faster turn around,
as well as a dried blood spot protocol for
applications requiring this type of specimen.
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Company:
Date:
November 10, 2008
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PRIMACY Medical is supplied as standard with the normal adjustable end cap, as illustrated, for conventional blood sampling form the finger tips. Instructions for this method of sampling are provided with the device.
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Company:
Date:
November 30, 2009
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Reliable & clear visible results in short time.
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Company:
Date:
April 26, 2010
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Reliable results in just 20 minutes
Greater than 99 accuracy
The only approved HIV-1/2 test for:
o Oral Fluid
o Plasma
o Venipuncture Whole Blood
o Fingerstick Whole Blood
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Company:
Date:
November 10, 2008
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The OraQuick® rapid test platform for fingerstick whole blood, has been appoved by the FDA for testing for HIV-1 antibodies. The company is working on extending the intended use of the device to other samples like oral fluid and serum/plasma for the presence of various antigens. After collection, the pad is inserted into a vial containing a pre-mixed amount of developer solution and allowed to develop.
When whole blood, serum or plasma is to be tested, a loop collection device is used to collect the sample and insert it into the developer solution, after which the collection pad is inserted in
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Company:
Date:
November 10, 2008
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The OraSure® Oral Specimen Collection Device is a generic device which was developed and FDA approved for the purpose of collecting, preserving, and transporting oral fluid specimens.
The OraSure device uses a simple, two minute collection procedure which can be performed by any trained personnel. It completely eliminates the risk associated with handling needles and blood.
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Company:
Date:
November 10, 2008
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