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6- Monoacetylmorphine 6- MAM Rdt Kit Of Drug Abuse Diagnosis 10ng / Ml

Product Details:

Place of Origin:China
Brand Name:AllTest
Certification:CE, ISO13485
Model Number:DAP-X14

Payment & Shipping Terms:

Minimum Order Quantity:N/A
Price:Negotiation
Packaging Details:25 cassette/box
Delivery Time:2-4 Weeks
Payment Terms:Ex works
Supply Ability:10 M tests/month
Detailed Product Description
Format: AllTest Specimen: Powder
Kit Size: 10 T/Kit Storage: 2-30℃
Cut-off: 10ng/ml Certificate: CE

 

High Quality 6-Monoacetylmorphine (6-MAM)  Drug Abuse Diagnosis 10ng/ml Test Panel Kit With CE 

 

Application And Description:  

 

6-Monoacetylmorphine (6-MAM) or 6-acetylmorphine (6-AM) is one of three active metabolites of heroin (diacetylmorphine), the others being morphine and the much less active 3-monoacetylmorphine (3-MAM). 6-MAM is rapidly created from heroin in the body, and thenis either metabolized into morphine or excreted in the urine. 6-MAM remains in the urine for no more than 24 hours. So a urine specimen must be collected soon after the last heroin use, but the presence of 6-MAM guarantees that heroin was in fact used as recently as within the last day. 6-MAM is naturally found in the brain, but in such small quantities that detection of this compound in urine virtually guarantees that heroin has recently been consumed.
The 6-MAM Rapid Test Cassette is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes a monoclonal antibody to selectively detect elevated levels of 6-MAM in urine. The 6-MAM Rapid Test Cassette yields a positive result when 6-MAM in urine reaches 10ng/ml. This is the suggested screening cut-off for positive specimens set by the Substance Abuse and Mental Health Services Administration (SAMHSA, USA).

 

How to use?

 

Test device (in closed pouches), samples, and controls should be brought to room temperature (15-30°C) prior to testing. Do not open pouches until ready to perform the assay.
Remove the test device from its protective pouch and label the device with patient’s identification or control label.
FOR SURFACES
1.Wipe with the panel over the surface in which the drugs are expected
2. Take off the cap of supplied tube;
3. Fill all buffers from the supplied tube of buffer into the protection cover.
4. Insert the Multi Test slowly and carefully into the protection cover with buffer
5. Wait for lines to appear on the membrane and read the results after 5 minutes and do not interpret the result after 10 minutes.

6- Monoacetylmorphine 6- MAM Rdt Kit Of Drug Abuse Diagnosis 10ng / Ml


FOR SOLIDS
1. Open the tube and put the solid in to the buffer.
2. Close the tube with dropper and cap. Shake it a short time. Wait for 30 sec.
3. Take off the cap of supplied tube;
4. Fill all buffers with dissolved substances into the protection cover.
5. Insert the Multi Test slowly and carefully into the protection cover with buffer.
6. Wait for lines to appear on the membrane and read the results after 5 minutes and do not interpret the result after 10 minutes.

6- Monoacetylmorphine 6- MAM Rdt Kit Of Drug Abuse Diagnosis 10ng / Ml

 

 

 

INTERPRETATION OF RESULTS
(Please refer to the illustration above)
6- Monoacetylmorphine 6- MAM Rdt Kit Of Drug Abuse Diagnosis 10ng / Ml

NEGATIVE:* A colored line appears in the Control region (C) and colored lines appear in the Test region (T). This negative result means that the concentrations in the sample are below the designated cut-off levels for a particular drug tested.


*NOTE: The shade of the colored lines(s) in the Test region (T) may vary. The result should be considered negative whenever there is even a faint line.

6- Monoacetylmorphine 6- MAM Rdt Kit Of Drug Abuse Diagnosis 10ng / Ml

POSITIVE: A colored line appears in the Control region (C) and NO line appears in the Test region (T). The positive result means that the drug concentration in the sample is greater than the designated cut-off for a specific drug.


6- Monoacetylmorphine 6- MAM Rdt Kit Of Drug Abuse Diagnosis 10ng / Ml

 

INVALID: No line appears in the Control region (C). Insufficient specimen volume or incorrect procedural techniques are the most likely reasons for Control line failure. Read the directions again and repeat the test with a new test card. If the result is still invalid, contact your manufacturer.

Contact Details
Hangzhou AllTest Biotech CO.,LTD

Tel:86-571-56267891

Fax:86-571-56267856

Contact Person: Mrs. Selina

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