Sciteck™ SVT™ Adulteration Specific Gravity Reagent

Description

For in vitro diagnostic use to determine specific gravity of solution

• Colorimetric: endpoint
• Based on pKa change of pretreated polyelectrolytes in response to ionic concentration of test sample
• Reaction produces a color change monitored at 600nm

Sciteck™ Specimen Validity Testing (SVT™)

• In accordance with SAMHSA's FWDTP guidelines as specified by Executive Order 12564 and delineated in the Federal Register Vol. 53 FR 11970-11989 and Vol. 59 FR 29908-29931; and other federally mandated programs (DOT, DOE, NRC and FHWA) for employment drug screening
• Sciteck evolved from Chimera Research, providing liquid reagents to laboratories for specimen validity testing in urine specimens submitted for DAU testing since 1989
• Adulteration testing products to include extensive SVT adulteration and EIA™ Drugs of Abuse single and multi-assay(s) (4-in-1™) reagent line
• SVT line consists of assays for pH, specific gravity, nitrite (non-corrosive), aldehydes, oxidants, chromate, creatinine, and halogens (bleach)
• AdultaCheck™ for on-site adulteration products

Specifications

• Content And Storage: 2°C to 10°C
• Type: SVT™ Specific Gravity Calibrator 1.005 and 1.030
• Intended Use: In-vitro diagnostic use to determine the specific gravity of a solution, forensic/toxicology use
• Quantity: 2 x 60 mL
• Source: Human Urine
• Wavelength: 600nm

U.S. and Foreign Patents Pending: 5,753,451.