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10ng/ML AB-PINACA ABP Drug Abuse Test Kit Urine Vitro Diagnostic

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10ng/ML AB-PINACA ABP Drug Abuse Test Kit Urine Vitro Diagnostic

City & Province	hangzhou zhejiang
Categories	Testing & Analyse Equipment

Product Details

Cassette / Dipstick / Panel Accurate Drug Abuse Test Kit Urine AB-PINACA (ABP) CE Certificate

Product features	Parameters
Principle	Chromatographic Immunoassay
Format	Dipstick, Cassette, Panel, Cup
Specimen	Urine
Certificate	CE
Reading Time	5 minutes
Pack	40T/50T
Storage Temperature	2-30°C
Shelf Life	2 Years
Sensitivity	92.00%
Specificity	97.10%
Accuracy	95.80%
Cut-Off	10 ng/mL*

AB-PINACA (ABP) rapid test for the qualitative detection of 10 ng/mL in human urine. For medical and other professional in vitro diagnostic use only.

Application:

The ABP Rapid Test Dipstick (Urine) is a rapid chromatographic immunoassay for the detection of AB-PINACA in human urine at a cut-off concentration of 10ng/mL.

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) or Liquid Chromatography/mass spectrometry (LC/MS) are the preferred confirmatory methods. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

Description:

AB-PINACA is a compound that was first identified as a component of synthetic can/nabis products in Japan in 2012. It was originally developed by Pfizer in 2009 as an analgesic medication.2 AB-PINACA acts as a potent agonist for the CB1 receptor (Ki = 2.87 nM, EC50 = 1.2 nM) and CB2 receptor (Ki = 0.88 nM, EC50 = 2.5 nM) and fully substitutes for Δ9-THC in rat discrimination studies, while being 1.5x more potent.

How to use?

Allow the test, urine specimen, and/or controls to reach room temperature (15-30°C) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test cassette from the sealed pouch and use it within one hour.

2. Place the test cassette on a clean and level surface. Hold the dropper vertically and transfer 3 full drops of urine (approx. 120μL) to the specimen well (S) of the test cassette, and then start the timer. Avoid trapping air bubbles in the specimen well (S). See the illustration below.

3. Wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10minutes.

DIRECTIONS FOR PANEL 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.
4. Replace the cap and place the test panel on a non-absorbent flat surface.
5. Start the timer and wait for the colored line(s) to appear.
6. The result should be read at 5 minutes. Do not interpret the result after 10 minutes.

DIRECTIONS FOR DIPSTICK 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 dipstick from the sealed pouch and use it within one hour.
2. With arrows pointing toward the urine specimen, immerse the test dipstick vertically in the urine specimen for at least 10-15 seconds. Do not pass the maximum line (MAX) on the Test Dipstick when immersing the strip. See the illustration below.
3. Place the test dipstick on a non-absorbent flat surface, start the timer and wait for the colored line(s) to appear. Read results at 5 minutes. Do not interpret the result after 10 minutes.

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 AB-PINACA (ABP) concentration is below the detectable 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 AB-PINACA (ABP) concentration is above the detectable 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 Cassette. If the problem persists, discontinue using the Test Cassette immediately and contact your local distributor.

Cat. No.	Product Description	Specimen	Format	Kit Size	Cut-Off	Status
Cat. No.	Product Description	Specimen	Format	Kit Size	Cut-Off	Status
DABP-102	AB-PINACA (ABP) Rapid Test Cassette	Urine	Cassette	40 T	10 ng/mL*	CE
DABP-114	AB-PINACA (ABP) Rapid Test Panel	Urine	Panel	40 T		CE
DABP-101	AB-PINACA (ABP) Rapid Test Dipstick	Urine	Dipstick	50 T		CE