Bovine Brucella Ab Test

General Information
Method: Double Antigens Sandwich Method
Sensitivity : 99.5%
Specificity : 98.8%
Specimen : Serum / Plasma
Reading Time : 5- 10 min

Canine brucella ab rapid test is a lateral flow immunoassay for quick detection of brucella canis in serum. Welcome your enquiry!

Specifications
Specimens: serum
Shelf life: 18 months
Storage temperature: room temperature(2-30c degree)

10 tests per kit, sealed in foil pouch

4. Centrifugal tubes (each containing 180 ¦ìl of assay buffer)
5. Product manual


Test procedure

1. Do centrifugation to cattle¡¯s whole blood sample to collect serum or plasma for use.
2. Use small pipette with reticle to transfer 20 ¦ìl (upper reticle) of serum or plasma into the centrifugal tube with assay buffer. Mix them well by the pipette attached in the pouch.
3. Take out the cassette from the foil pouch and place it horizontally.
4. Drip 3 drops (about 100 ¦ìl) of sample mixture into the sample hole.
5. Interpret the result in 5-10 minutes. Result after 10 minutes is considered as invalid.

Interpretation of results

Positive: the presence of both c band and t band, no matter t band is clear or vague.
Negative: only clear c band appears.
Invalid: no colored band appears in c zone, no matter whether t band appears.



Storage

The kit can be stored at room temperature (2-30¡ãc). The test kit is stable through the expiration date (18 months) marked on the foil pouch. Do not freeze. Do not store the test kit in direct sunlight.


Precaution

1. For best results, please strictly adhere to these instructions.
2. All reagents must be at room temperature before running the assay.
3. Do not remove test cassette from its pouch until immediately before use.
4. Do not reuse the test kit.
5. Do not use the test beyond its expiration date marked on the foil pouch.
6. The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.

Limitation

Bovine tuberculosis ab rapid test is for in vitro veterinary diagnosis use only. All results should be considered with other clinical information available from veterinarian. For an accurate result, it is suggested to apply other method such as elisa for final determination in practice.




In house standard

The H pylori can be utilized as a rapid screening process for large populations of patients and highly indicated in the early diagnosis of H pylori infection as the immune response can often precede clinical manifestations of disease From a diagnostic point of view, a high serum level specific antibodies against H pylori must be interpreted as an indication of type B asymptomatic gastritis

Specification:
Specimen:Serum/plasma/whole blood
Sensitivity:96%
Specificity:90%
Packaging:25 cassettes/box,
Certificate:CE and ISO 13485
Raw materials is imported from US
OEM packaging is available

KOSTEC can supply Korean rapid test kits, which are not only faster and easier in test but alsoprovide accurater test results. Also price is very much attractive! If you have any interest in this test kits, do not hesitate to contact me. Thanks!

Product Details:

Number of Reactions(Preps)/Kit :30T
Brand : SD Biosensor
ICMR Approved : Yes
Result Time (Rapid Kits) : 10 min
CAT No : RK019-30
STANDARD Q HIV 1/2 Ab 3-Line performs qualitative analysis by detecting antibodies specific to HIV-1 (including Group O) and HIV-2 in serum, plasma and whole blood using immunochromatography. With a simple test method, HIV infection status can be discriminated, and with its high sensitivity and specificity, the screening test result can be obtained within 10 minutes.

Easy to use, Easy to read and interpret
Discrimination between HIV-1 and HIV-2 antibodies
Room temperature storage
Performance
Sensitivity : 100% (74/74)/ Specificity : 100% (232/232)

The Chagas Ab Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of IgG anti-Trypanosoma cruzi (T. cruzi) in human serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with T. cruzi. Any reactive specimen with the Chagas Ab Rapid Test must be confirmed with alternative testing method(s) and clinical findings.

Chagas disease is an insect-borne, zoonotic infection by the protozoan T. cruzi, which causes a systemic infection of humans with acute manifestations and long term sequelae. It is estimated that 16-18 million individuals are infected worldwide, and roughly 50,000 people die each year from chronic Chagas disease (World Health Organization)1.

Buffy coat examination and xenodiagnosis used to be the most commonly methods2,3 in the diagnosis of acute T. cruzi infection. However, both methods are either time consuming or lack of sensitivity. Recently, serological test becomes the mainstay in the diagnosis of Chagasâ??s disease. In particularly, recombinant antigen based tests eliminate false-positive reactions which are commonly seen in the native antigen tests4-5.

The Chagas Ab Rapid Test is an instant antibody test which detects IgG antibodies the T. cruzi within 15 minutes without any instrument requirements. By utilizing T. cruzi specific recombinant antigen, the test is highly sensitive and specific.

INTENDED USE

Feline Immunodeficiency Virus Ab Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of Feline Immunodeficiency Virus antibody (FIV Ab) in cat's blood.

PRINCIPLE OF THE ASSAY

Feline Immunodeficiency Virus Ab Test is based on sandwich lateral flow immunochromatographic assay. The test device has a testing window. The testing window has an invisible T (test) zone and C (control) zone. When sample is applied into the sample hole on the device, the liquid will laterally flow on the surface of the test strip. If there is enough FIV antibody in the sample, a visible T band will appear. The C band should always appear after a sample is applied, indicating a valid result. By this means, the device can accurately indicate the presence of FIV antibody in the sample.

INTERPRETATION OF RESULTS

Positive: The presence of both C band and T band, no matter T band is clear or vague.

Negative: Only clear C band appears.

Invalid: No colored band appears in C zone, no matter whether T band appears.

STORAGE

The kit can be stored at room temperature (2-30C). The test kit is stable through the expiration date (18 months) marked on the foil pouch. DO NOT FREEZE. Do not store the test kit in direct sunlight.

1. The One Step RV IgG/IgM Test can be performed used on Whole Blood /Serum / Plasma.
2. To collect whole blood, serum or plasma specimens following regular clinical laboratory procedures.
3. Testing should be performed immediately after specimen collection. Do not leave the specimens at room temperature for prolonged periods. For long term storage, specimens should be kept below -20â??. Whole blood should be stored at 2-8â?? if the test is to be run within 2 days of collection. Do not freeze whole blood specimens.
4. Bring specimens to room temperature prior to testing. Frozen specimens must be completely thawed and mixed well prior to testing. Specimens should not be frozen and thawed repeatedly.
Test Procedure
Allow the test, specimen, buffer and/or controls to reach room temperature 15-30â?? (59-86â??) prior to testing.
1. Bring the pouch to room temperature before opening it. Remove the test device from the sealed pouch and use it as soon as possible.
2. Place the test device on a clean and level surface.
3. Hold the dropper vertically and transfer 1 drop of specimen (approximately 10μl) to the specimen well(S) of the test device, then add 2 drops of buffer (approximately 80μl) and start the timer. See illustration below.
4. Wait for the colored line(s) to appear. Read results at 15 minutes. Do not interpret the result after 20 minutes.
Interpretation of Results
Positive: Control line and at least one test line appear on the membrane. The appearance of T2 test line indicates the presence of RV specific IgG antibodies. The appearance of T1 test line indicates the presence of RV specific IgM antibodies. And if both T1 and T2 line appear, it indicates that the presence of both RV specific IgG and IgM antibodies. The lower the antibody concentration is, the weaker the result line is.
Negative: One colored line appears in the control region(C). No apparent colored line appear in the test line region.
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 device. If the problem persists, discontinue using the test kit immediately and contact your local distributor.