Anuradha Enterprises

• Specimen 

  Whole blood, serum, plasma

• Test time 

  15-20mins (Inaccurate results after 20 minutes)

• Sensitivity 

  92.9% (184/198)

• Specificity 

  98.7% (222/225)

• Storage temperature 

  2-40℃ / 36-104℉

The test is designed to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with dengue virus.

Any use or interpretation of this preliminary test result must also rely on other clinical findings and the professional judgment of health care providers. Alternative test method(s) should be considered to confirm the test result obtained by this device.

Recommended for use:

Any person presenting with clinical signs or symptoms within 9 days consistent with acute dengue infection or dengue fever including: high fever, severe headaches, severe pain behind the eyes, severe joint and muscle pain, fatigue, nausea, vomiting, and/or skin rash.

Dengue NS1 antigen is detectable in human blood from the first day after the onset of fever up to 9 days, which allows early detection and prompt treatment of infection with dengue virus.

This test is intended to be used for the simultaneous detection and differentiation of IgG and IgM antibodies to Leptospira interrogans (L. interrogans) in human serum, plasma or whole blood. It is intended to be used as a screening test by professionals, and provides a preliminary test result to aid in the diagnosis of infection with L. interrogans. Any interpretation or use of this test result must also rely on other clinical findings as well as on the professional judgment of health care providers.

Recommended for use:

• Accuracy: 100% specificity and 100% sensitivity in comparison with a reference rapid test on the market
• Cross Reactivity: No false positive results were observed on specimens from TP, HIV, Dengue, TB, Typhoid Ab , HBsAg, HCV Ab, HEV Ab, H.P Ab, HAV, HCG, RF, ANA, HAMA
• Interference: No interference were seen with substances: Salicylic acid: 4.34 mmol/L; Glucose: 55 mmol/L; Sodium citrate: 3.8 %; Heparin: 3,000 U/L;  Creatinine:  442 μmol/L; Bilirubin:  20 mg/dL; EDTA: 3.4 μmol/L; Hemoglobin: 2g/L; Human IgG: 1000 mg/dL; AlbuminL 60 g/L
• Shelf life: 24 month
• Individually sealed foil pouches containing:
  • One cassette device
  • One desiccant
• 5 μL capillary tubes
• Sample diluent (REF SB-R0101, 5 mL/bottle)
• One package insert (instruction for use)

Product Details:-
STANDARD Q Dengue NS 1 Ag qualitatively analyzes NS1 antigens specific to Dengue virus in serum, plasma and whole blood using immunochromatography. By detecting Dengue NS1 antigens, the initial infection status of Dengue virus can be discriminated, and the screening test result can be obtained within 15 minutes with its high sensitivity and specificity.
Note:
One Step Rapid, immunochromatographic test for the detection dengue NS1 Ag in human serum, plasma or whole blood

Products available as per the customer requirement, Our products is highly appreciated by customers.

Products available as per the customer requirement, Our products is highly appreciated by customers.A rapid antigen test (RAT), sometimes called a rapid antigen detection test (RADT), antigen rapid test (ART), or loosely just a rapid test, is a rapid diagnostic test suitable for point-of-care testing that directly detects the presence or absence of an antigen. RATs are a type of lateral flow test detecting antigens, rather than antibodies (antibody tests) or nucleic acid (nucleic acid tests). Rapid tests generally give a result in 5 to 30 minutes, require minimal training or infrastructure, and have significant cost advantages.[citation

TRUSTwell AntiMullerian hormone AMH ELISA kitAccuracy: R2 = 0.918 with CLIA as reference.

Analytical Sensitivity: 1.2 ng/mL.

Specificity: No cross-reactivity to non-hydroxylated vitamin D2 and Vitamin D3.

Intra & Inter-assay precision: CV <=10%.

Higher linearity: 0-150 ng/mL.

1 step less procedure, faster result.

High & Low level assay controls included.

Accuracy: R2 = 0.918 with CLIA as reference.

Analytical Sensitivity: 1.2 ng/mL.

Specificity: No cross-reactivity to non-hydroxylated vitamin D2 and Vitamin D3.

Intra & Inter-assay precision: CV <=10%.

Higher linearity: 0-150 ng/mL.

1 step less procedure, faster result.

High & Low level assay controls included