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Point-of-care testing (POCT), or bedside testing is defined as medical diagnostic testing at or near the point of care—that is, at the time and place of patient care.[1] This contrasts with the historical pattern in which testing was wholly or mostly confined to the medical laboratory, which entailed sending off specimens away from the point of care and then waiting hours or days to learn the results, during which time care must continue without the desired information.
 
Point-of-care tests are simple medical tests that can be performed at the bedside. In many cases the simplicity was not achievable until technology developed not only to make a test possible at all but then also to mask its complexity. For example, various kinds of urine test strips have been available for decades, but portable ultrasonography did not reach the stage of being advanced, affordable, and widespread until the 2000s and 2010s. Today portable US is often viewed as a "simple" test, but there was nothing simple about it until the more complex technology was available. Similarly, pulse oximetry can test arterial oxygen saturation in a quick, simple, noninvasive, affordable way today, but in earlier eras this required an intraarterial needle puncture and a laboratory test; and rapid diagnostic tests such as malaria antigen detection tests rely on a state of the art in immunology that did not exist until recent decades. Thus, over decades, testing continues to move toward the point of care more than it formerly had been. A recent survey in five countries (Australia, Belgium, the Netherlands, the UK and the US) indicates that general practitioners / family doctors would like to use more POCTs.
 
The driving notion behind POCT is to bring the test conveniently and immediately to the patient. This increases the likelihood that the patient, physician, and care team will receive the results quicker, which allows for better immediate clinical management decisions to be made. POCT includes: blood glucose testing, blood gas and electrolytes analysis, rapid coagulation testing (PT/INR, Alere, Microvisk Ltd), rapid cardiac markers diagnostics (TRIAGE, Alere), drugs of abuse screening, urine strips testing, pregnancy testing, fecal occult blood analysis, food pathogens screening, hemoglobin diagnostics (HemoCue), infectious disease testing and cholesterol screening.
 
POCT is often accomplished through the use of transportable, portable, and handheld instruments (e.g., blood glucose meter, nerve conduction study device) and test kits (e.g., CRP, HBA1C, Homocystein, HIV salivary assay, etc.). Small bench analyzers or fixed equipment can also be used when a handheld device is not available—the goal is to collect the specimen and obtain the results in a very short period of time at or near the location of the patient so that the treatment plan can be adjusted as necessary before the patient leaves. Cheaper, faster, and smarter POCT devices have increased the use of POCT approaches by making it cost-effective for many diseases, such as diabetes, carpal tunnel syndrome (CTS) and acute coronary syndrome. Additionally, it is very desirable to measure various analytes simultaneously in the same specimen, allowing a rapid, low-cost, and reliable quantification. Therefore, multiplexed point-of-care testing (xPOCT) has become more important for medical diagnostics in the last decade.
MSLRDT007 HIV 1.2.O Rapid Test Cassette
Product Name:  MSLRDT007 HIV 1.2.O Rapid Test Cassette
Latest Price:
Model No.:  MSLRDT007
Weight:  Net weight: Kg
Minimum Order Quantity:  1 Set Set/Sets
Supply Ability:  300 Sets per Year
Payment Terms:  T/T,L/C,D/A,D/P,Western Union,MoneyGram,PayPal
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Quick Details

1. Fast: get the result in 10 mins.

2. High sensitivity and specificity.

3. Simple to use.

4. Accurate and reliable.

5. Ambient storage.

6. Early screening of HIV-1, HIV-2 and Subtype O infection, suitable for African region.

Packaging & Delivery

Packaging detail:Standard export package
Delivery detail:within 7-10 workdays after receipt of payment

Specifications

MSLRDT007 HIV 1.2.O Rapid Test Cassette

1. Fast: get the result in 10 mins.

2. High sensitivity and specificity.

3. Simple to use.

4. Accurate and reliable.

5. Ambient storage.

6. Early screening of HIV-1, HIV-2 and Subtype O infection, suitable for African region.

Catalog No.

MSLRDT007

Product name

HIV 1.2.O Rapid Test Cassette (Whole Blood/Serum/Plasma)

Analyte

HIV-1, HIV-2, Subtype O

Test method

Colloidal Gold

Sample type

WB/Serum/Plasma

Sample volume

1 drop of serum/plasma, 2 drops of WB

Reading time

10 mins

Sensitivity

>99.9%

Specificity

99.9%

Storage

2~30℃

Shelf life

24 months

Qualification

/

Format

Cassette

Package

40T/kit

hiv test

MSLRDT007 HIV 1.2.O Rapid Test Cassette

PRINCIPLE

The HIV  1.2.O  Rapid Test  Cassette (Whole  Blood/Serum/Plasma) is  a qualitative,  membrane based

immunoassay for the detection  of antibodies to HIV-1,  HIV-2, and Subtype O in whole  blood, serum or

plasma. The membrane is pre-coated with recombinant HIV  antigens in the test line regions, T1 and T2.

The T1 test line is  pre-coated with HIV-1 and Subtype O antigen and the  T2 test line is pre-coated with

HIV-2  antigen. During  testing, the  whole  blood, serum  or  plasma specimen  reacts with  HIV  antigen

The following potentially interfering substances were added to HIV negative and positive specimens.

chromatographically by  capillary action and  reacts with recombinant  HIV antigen on  the membrane  in

the  test line  region.  If the  specimen  contains antibodies  to  HIV-1 and/or  Subtype  O, or  HIV-2,  one

colored  line will  appear  in the  test  line region;  if  the specimen  contains  antibodies  to HIV-1  and/or

Subtype  O, and  HIV-2, two  colored lines  will  appear in  the test  line region.  Both  indicate a  positive

result. If the specimen  does not contain HIV-1, Subtype O, and/or HIV-2  antibodies, no colored line will

appear in  the test line  region indicating a  negative result. To  serve as a  procedural control, a  colored

line will  always appear  in the control  line region  indicating that  proper volume of  specimen has  been

added and membrane wicking has occurred.

REAGENTS

The test  contains HIV  type 1, type  2, and  Subtype O  recombinant antigens coated  particles and HIV

type 1, type 2, and Subtype O recombinant antigens coated on the membrane.

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