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Steroid Testing Kit Drug Abuse Test Kit For Zolpidem Qualitative Detection

Product Details:

Place of Origin:CHINA
Brand Name:AllTest
Certification:CE, FDA 510K
Model Number:cassette

Payment & Shipping Terms:

Minimum Order Quantity:500
Packaging Details:50T/Kit,40T/kit,25T/kit
Supply Ability:100 Million a year
Detailed Product Description
Format: Dipstick,Cassette, Panel Specimen: Urine
Kit Size: 50T/Kit,40T/kit,25T/kit Cut-Off: 50 Ng/mL
Storage: 2-30℃ Shelf Time: 24 Months

 

A rapid test for the qualitative detection of Zolpidem in human urine. For professional CE certified

 

 

Applications: 

 

The ZOL Rapid Test Panel is a rapid chromatographic immunoassay for the detection of Zolpidem in human urine at the cut-off concentration of 50ng/ml. Please refer to Analytical Specificity table in this package insert for details on reactivity.

This assay provides only a qualitative, preliminary, analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. Gas chromatography/mass spectrometry (GC/MS) is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

 

 

Description: 

 

Zolpidem (brand names Ambien, Ambien CR, Intermezzo, Stilnox, Stilnoct, Sublinox, Hypnogen, Zonadin, Sanval and Zolsana) is a prescription medication used for the treatment of insomnia and some brain disorders.1 It is a short-acting nonbenzodiazepine hypnotic of the imidazopyridine class.1

That potentiates GABA, an inhibitory neurotransmitter, by binding to GABA receptors at the same location as benzodiazepines.2 It works quickly, usually within 15 minutes, and has a short half-life of two to three hours.

Zolpidem may be detected in blood or plasma to confirm a diagnosis of poisoning in hospitalized patients, provide evidence in an impaired driving arrest, or to assist in a medico-legal death investigation. Blood or plasma Zolpidem concentrations are usually in a range of 30–300 μg/l in persons receiving the drug therapeutically, 100–700 μg/l in those arrested for impaired driving, and 1000–7000 μg/l in victims of acute overdosage. Analytical techniques, in general, involve gas or liquid chromatography.3,4,5

The ZOL Rapid Test Panel is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes monoclonal antibodies to selectively detect elevated levels of Zolpidem in urine. The ZOL Rapid Test Panel yields a positive result when Zolpidem in urine reaches 50ng/ml.

 

 

How to use? 

 

Allow the test, urine specimen, and/or controls to reach room temperature (15-30ºC) prior to testing.

  1. Bring the pouch to room temperature before opening it. Remove the test panel from the sealed pouch and use it within one hour.
  2. Remove the cap.
  3. With the arrow pointing toward the urine specimen, immerse the test panel vertically in the urine specimen for at least 10 to 15 seconds. Immerse the strip to at least the level of the wavy lines, but not above the arrow on the test panel.
Steroid Testing Kit Drug Abuse Test Kit For Zolpidem Qualitative Detection

 

 

INTERPRETATION OF RESULTS

 

(Please refer to the illustration above)

 

NEGATIVE:* Two lines appear. One color line should be in the control region (C), and another apparent color line should be in the test region (T). This negative result indicates that the Zolpidem concentration is below the detectable cutoff level.

 

*NOTE:  The shade of color in the test region (T) may vary, but it should be considered negative whenever there is even a faint color line.

 

POSITIVE: One color line appears in the control region (C). No line appears in the test region (T). This positive result indicates that the Zolpidem concentration is above the detectable cutoff level.

 

INVALID: Control line fails to appear. Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for control line failure. Review the procedure and repeat the test with a new test Panel. If the problem persists, discontinue using the test Panel immediately and contact your local distributor.

 

QUALITY CONTROL

 

A procedural control is included in the test. A color line appearing in the control region (C) is considered an internal procedural control. It confirms sufficient specimen volume and correct procedural technique.

Control standards are not supplied with this test Panel; however it is recommended that positive and negative controls be tested as good laboratory testing practices to confirm the test procedure and to verify proper test performance.

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Tel:86-571-56267891

Fax:86-571-56267856

Contact Person: Mrs. Selina

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