Giardia (GIA) is a common intestinal parasitic protozoan that is susceptible to both humans and pets. Giardia is most commonly found in dogs and occasionally in cats.
This kit is used for the detection of Giardia antigen in the feces of canine and feline, and can be used for the screening and auxiliary diagnosis of Giardia infection in canine and feline.

Test principle of the GIA-Ag Test Kit

This product uses rapid immunochromatography technology to detect Giardia antigen in the feces of canine and feline. After the diluted sample was dropped into the sample well, if there was GIA antigen in the sample, it would specifically bind to the recombinant protein labeled with colloidal gold to form a complex that moved along the chromatographic membrane and was captured by GIA antibody coated on the membrane, showing a Burgundy line on the detection line (T). If the GIA antigen is not present in the sample, no visible lines are formed at the T position. No matter the result is negative or positive, the C line should be colored, otherwise the result is invalid.

Sample Requirements

1. Please refer to the instructions for use
2. This kit is only suitable for testing feline whole blood or serum samples (hemolysis and hyperlipidemia samples cannot be used).
3. Collect fresh samples and immediately put into the extraction buffer solution, which should be detected as soon as possible within 1 hour.
4. If samples were not timely detected, store within 24 hours at 2-8°C and store within 1 month at -20°C.

Product Performance Indifelineors

1. Sensitivity ≥ 95%.
2. Specificity ≥ 97.5%.
3. Precision: no more than one false negative and false positive results within the batch; the test lines & control line (cards) between three lots shall be uniform, and no more than one time of color difference between lots.
4. Stability: valid for 24 month if unopened & store 2-30°C.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appear next to “C”.
Positive: In the test window, two distinct colored lines appear next to “T” & “C” simultaneously.
Invalid: No color line visible next to “C”.

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Canine Adenovims TypeⅠbelongs to the family Adenoviridae, the genus of mammalian adenovirus in the classification. It causes canine infectious hepatitis, (an acute septic infectious disease characterized by central necrosis of liver lobules, inclusion bodies in the nuclei of liver parenchymal cells and cortical cells, and prolonged hemorrhage.)
This kit is used to detect canine adenovirus typeⅠantigen in the secretions from the eyes, nose and mouth of dogs, and to screen and assist in the diagnosis of canine adenovirus typeⅠ infection.

Test principle of the CAVⅠ-Ag Test Kit

This product uses rapid immunochromatography technology to detect canine adenovirus type I antigen in the secretions of the eyes, nose and mouth of dogs. If there was CAV I antigen in the sample, it would specifically bind to the recombinant protein labeled with colloidal gold to form a complex that moved along the chromatographic membrane and was captured by CAV I antibody coated on the membrane, showing a wine red line on the detection line (T). If the CAV I antigen is not present in the sample, no visible lines are formed at the T position. No matter the result is negative or positive, the C line should be colored, otherwise the result is invalid.

Sample Requirements

1. Please refer to the instructions for use
2. This kit is only suitable for testing feline whole blood or serum samples (hemolysis and hyperlipidemia samples cannot be used).
3. Collect fresh samples and immediately put into the extraction buffer solution, which should be detected as soon as possible within 1 hour.
4. If samples were not timely detected, store within 24 hours at 2-8°C and store within 1 month at -20°C.

Product Performance Indifelineors

1. Sensitivity ≥ 95%.
2. Specificity ≥ 97.5%.
3. Precision: no more than one false negative and false positive results within the batch; the test lines & control line (cards) between three lots shall be uniform, and no more than one time of color difference between lots.
4. Stability: valid for 24 month if unopened & store 2-30°C.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appear next to “C”.
Positive: In the test window, two distinct colored lines appear next to “T” & “C” simultaneously.
Invalid: No color line visible next to “C”.

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Canine rotavirus is highly resistant to commonly used disinfectants and can survive for months in feces. The specific symptoms of infected canine rotavirus are highly dependent on their age.

This kit detects canine rotavirus antigen in dog feces or vomit and is used for screening and auxiliary diagnosis of canine rotavirus infection.

Test principle of the CRV-Ag Test Kit

This product uses a rapid immunochromatographic technique for the detection of canine rotavirus antigens in canine feces or vomit. If there is CRV antigen in the sample, it will specifically bind to the recombinant protein labeled with colloidal gold to form a complex that will move along the chromatographic membrane and be captured by the CRV antibody coated on the membrane, showing a wine red line on the detection line (T). If the CRV antigen is not present in the sample, no visible line is formed at the T position. No matter the result is negative or positive, the C line should be colored, otherwise the result is invalid.

Sample Requirements

1. Please refer to the instructions for use
2. This kit is only suitable for testing feline whole blood or serum samples (hemolysis and hyperlipidemia samples cannot be used).
3. Collect fresh samples and immediately put into the extraction buffer solution, which should be detected as soon as possible within 1 hour.
4. If samples were not timely detected, store within 24 hours at 2-8°C and store within 1 month at -20°C.

Product Performance Indifelineors

1. Sensitivity ≥ 95%.
2. Specificity ≥ 97.5%.
3. Precision: no more than one false negative and false positive results within the batch; the test lines & control line (cards) between three lots shall be uniform, and no more than one time of color difference between lots.
4. Stability: valid for 24 month if unopened & store 2-30°C.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appear next to “C”.
Positive: In the test window, two distinct colored lines appear next to “T” & “C” simultaneously.
Invalid: No color line visible next to “C”.

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Rabies virus belongs to the genus Lyssavirus of the family Rhabdoviridae. It is the pathogen that causes rabies.
This kit is used for the detection of rabies virus antigen in the saliva of canine and feline, and for the screening and auxiliary diagnosis of rabies virus infection in canine and feline.

Test principle of the RBV-Ag Test Kit

This product uses rapid immunochromatography technology to detect rabies virus antigen in the saliva of canine and feline. If the RBV antigen was present in the sample, it would specifically bind to the recombinant protein labeled with colloidal gold to form a complex that moved along the chromatographic membrane and was captured by the RBV antibody coated on the membrane, showing a wine red line on the detection line (T). If the RBV antigen is not present in the sample, no visible lines are formed at the T position. No matter the result is negative or positive, the C line should be colored, otherwise the result is invalid.

Sample Requirements

1. Please refer to the instructions for use
2. This kit is only suitable for testing feline whole blood or serum samples (hemolysis and hyperlipidemia samples cannot be used).
3. Collect fresh samples and immediately put into the extraction buffer solution, which should be detected as soon as possible within 1 hour.
4. If samples were not timely detected, store within 24 hours at 2-8°C and store within 1 month at -20°C.

Product Performance Indifelineors

1. Sensitivity ≥ 95%.
2. Specificity ≥ 97.5%.
3. Precision: no more than one false negative and false positive results within the batch; the test lines & control line (cards) between three lots shall be uniform, and no more than one time of color difference between lots.
4. Stability: valid for 24 month if unopened & store 2-30°C.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appear next to “C”.
Positive: In the test window, two distinct colored lines appear next to “T” & “C” simultaneously.
Invalid: No color line visible next to “C”.

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Infectious canine hepatitis (ICH) is an acute, septic infectious disease caused by the canine hepatitis virus and characterized by hemorrhagic gastroenteritis, circulatory disturbance, centrilobular necrosis, and intranuclear inclusion bodies in liver parenchyma and endothelial cells.

This kit detects hepatitis antigens in canine fece, mouth, eye, and nose secretions and is used for screening and auxiliary diagnosis of canine hepatitis infection.

Test principle of the ICH-Ag Test Kit

This product uses rapid immunochromatography technology to detect canine hepatitis antigen in canine fece, mouth, eye and nose secretions. If ICH antigen is present in the sample, it will specifically bind to the recombinant protein labeled with colloidal gold to form a complex that moves along the chromatographic membrane and is captured by the ICH antibody coated on the membrane, showing a wine red line on the detection line (T). If there is no ICH antigen in the sample, no visible lines will form at the T position. No matter the result is negative or positive, the C line should be colored, otherwise the result is invalid.

Sample Requirements

1. Please refer to the instructions for use
2. This kit is only suitable for testing feline whole blood or serum samples (hemolysis and hyperlipidemia samples cannot be used).
3. Collect fresh samples and immediately put into the extraction buffer solution, which should be detected as soon as possible within 1 hour.
4. If samples were not timely detected, store within 24 hours at 2-8°C and store within 1 month at -20°C.

Product Performance Indifelineors

1. Sensitivity ≥ 95%.
2. Specificity ≥ 97.5%.
3. Precision: no more than one false negative and false positive results within the batch; the test lines & control line (cards) between three lots shall be uniform, and no more than one time of color difference between lots.
4. Stability: valid for 24 month if unopened & store 2-30°C.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appear next to “C”.
Positive: In the test window, two distinct colored lines appear next to “T” & “C” simultaneously.
Invalid: No color line visible next to “C”.

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Feline Infectious Peritonitis FIP belongs to the family Coronaviridae and the genus Coronavirus.

This kit can be used to detect feline infectious peritonitis antibody in feline blood or serum, and can be used for feline AIDS infection screening and auxiliary diagnosis.

Test principle of the Feline FIP-Ab Test Kit

This product uses a rapid immunochromatographic technique for the detection of antibodies to feline infectious peritonitis in feline whole blood or serum. If the FIP antibody was present in the sample, it would bind specifically to the recombinant protein labeled with colloidal gold to form a complex that moved along the chromatographic membrane and was captured by the FIP antigen coated on the membrane, showing a wine red line on the detection line (T). If the FIP antibody is not present in the sample, no visible line is formed at the T position. No matter the result is negative or positive, the C line should be colored, otherwise the result is invalid.

Sample Requirements

1. Please refer to the instructions for use
2. This kit is only suitable for testing feline whole blood or serum samples (hemolysis and hyperlipidemia samples cannot be used).
3. Collect fresh samples and immediately put into the extraction buffer solution, which should be detected as soon as possible within 1 hour.
4. If samples were not timely detected, store within 24 hours at 2-8°C and store within 1 month at -20°C.

Product Performance Indifelineors

1. Sensitivity ≥ 95%.
2. Specificity ≥ 97.5%.
3. Precision: no more than one false negative and false positive results within the batch; the test lines & control line (cards) between three lots shall be uniform, and no more than one time of color difference between lots.
4. Stability: valid for 24 month if unopened & store 2-30°C.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appears next to “C”
Positive: In the test window, two distinct colored lines appear simultaneously next to “T” & “C”
Invalid: no color line visible next to “C”

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Canine Parvovirus (CPV) belongs to the Parvoviridae family, the genus Parvovirus. Canine parvovirus is highly resistant to commonly used disinfectants and can survive in feces for months to years. Canine parvovirus is highly contagious and can be infected by dogs of different ages, genders and breeds, especially juvenile puppies.

Dogs infected with canine parvovirus have acute onset and high mortality. Clinical manifestations are vomiting and diarrhea. This kit detects parvovirus antibodies by detecting canine whole blood, serum or plasma.

Test principle of the CPV-Ab Test Kit

The kit is made by the principle of colloidal gold immunochromatography. After the sample is added to the sample hole, it moves along the chromatographic membrane together with the colloidal gold marker. If there is CPV antibody in the sample, the detection line will display purple-red. If there is no CPV in the sample Antibodies do not produce a color reaction.

The Canine Parvovirus test kit is able to detect Canine Parvovirus antigen concentration, demonstrating quantitative results. The test serves only as an aid to the diagnosis. For professional use only. And the quantitative results are trackable.

Intend Use

For rapid screening of Canine Parvovirus in canine whole blood, serum, or plasma (CPV).

Sample Requirements

1. This Canine Adenovirus Antigen Test Kit is only suitable for testing canine whole blood, serum or plasma samples.
2. The sample for the test must be collected immediately, the sample should be put into the dilution solution immediately after sampling, and the diluted sample should be tested as soon as possible, within 1 hour.
3. Diluted samples can be stored at 2-8°C for 24 hours and can be stored at -20°C for one month.

How to Use Canine Parvovirus Antibody Test Kit

1. Collect dog whole blood, serum or plasma samples, add the samples to the diluent after collection, tighten the lid, and mix by inversion.
2. Tear open the aluminium foil bag of the test card, take out the test card, and put it on a flat and clean table.
3. Pipe 3 drops of sample solution (about 80μL), and add to the sample well of the test card.
4. Read test results within 10-15 min at room temperature, and those results beyond 20 min are invalid.

Note: The above reading time is conducted at the room temperature of 15-30℃. If the temperature is lower than 15℃, the reading time should be extended. If the temperature is higher than 30℃, the reading time should be shortened.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appears next to “C”.
Positive: In the test window, two distinct colored lines appear simultaneously next to “T” & “C”.
Invalid: no color line visible next to “C”.

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Interpretation of Test Results

1. The negative test results indicate the absence of canine parvovirus antibody in the samples. The infection cannot be ruled out if the corresponding acute symptoms occur.
2. The test results were positive, indicating samples containing canine parvovirus antibody
3. Multiple reasons may cause invalid results and should be re-tested.

Limitations of Canine Parvovirus Antibody Test Kit

• This kit can only detect the presence of canine parvovirus antibody in the samples examined.
• The test results are for clinical reference only and are not the basis for diagnosis.

Canine adenovirus (CAV) is the most pathogenic of the mammalian adenovirus genus. There are two serotypes. Type I can cause both canine infectious hepatitis (an acute septic infectious disease characterized by central necrosis of the liver lobules, the appearance of inclusion bodies in the nuclei of liver parenchymal cells and cortical cells, and prolonged hemorrhage.) It can also cause fox encephalitis, so it is also called fox encephalitis and canine infectious hepatitis disease. Type II can cause canine infectious laryngotracheitis and enteritis. The Canine Adenovirus Antigen Test Kit is used to detect canine adenovirus antigens in canine eye secretions, nasal fluid, and saliva.

Test principle of the CAV-Ag Test Kit

The Canine Adenovirus Antigen Test Kit uses a rapid immunochromatographic assay to detect canine adenovirus antigens. You add a sample of your dog’s eye discharge, nasal fluid, or saliva to the spiking well of the test strip and move it along the chromatographic membrane with a colloidal gold-labeled anti-CAVt monoclonal antibody. If the CAV antigen is present in the sample, it will show red when bound to the antibody on the detection line. No color reaction is produced if the CAV antigen is not present in the sample.

The Canine Adenovirus Antigen Test Kit is able to detect Canine Adenovirus antigen concentration, demonstrating quantitative results. The test serves only as an aid to the diagnosis. For professional use only.

Intend Use

For rapid screening of Canine Adenovirus in canine eye secretions, nasal fluid, saliva and vomit. (CAV).

Sample Requirements

1. This Canine Adenovirus Antigen Test Kit is only suitable for testing eye secretions, nasal fluids, and saliva samples from dogs.
2. The sample for the test must be collected immediately, the sample should be put into the dilution solution immediately after sampling, and the diluted sample should be tested as soon as possible, within 1 hour.
3. Diluted samples can be stored at 2-8°C for 24 hours and can be stored at -20°C for one month.

How to Use Canine Adenovirus Antigen Test Kit

1. Disposable swabs were used to collect samples of eye secretions, nasal fluids, and saliva from the dogs, and then the swabs were placed in the diluted solution and mixed and left to stand for 1 minute. Remove the swab, tighten the cap, and turn the sample tube upside down to mix.
2. Tear open the aluminium foil bag of the test card, take out the test card, and put it on a flat and clean table.
3. Pipe 3 drops of sample solution (about 80μL), and add to the sample well of the test card.
4. Read test results within 10-15 min at room temperature, and those results beyond 20 min are invalid.

Note: The above reading time is conducted at the room temperature of 15-30℃. If the temperature is lower than 15℃, the reading time should be extended. If the temperature is higher than 30℃, the reading time should be shortened.

Interpretation of Results

Negative: In the test window, only one fuchsia-colored line appears next to “C”.
Positive: In the test window, two distinct colored lines appear simultaneously next to “T” & “C”.
Invalid: no color line visible next to “C”.

NOTE: Invalid test results can be caused by various reasons and should be re-tested.

Interpretation of Test Results

1. The negative test results indicate the absence of canine adenovirus antigen in the samples. The infection cannot be ruled out if the corresponding acute symptoms occur.
2. The test results were positive, indicating samples containing canine adenovirus.
3. Multiple reasons may cause invalid results and should be re-tested.

Limitations of Canine Adenovirus Antigen Test Kit

• This kit can only detect the presence of canine adenovirus antigen in the samples examined.
• The test results are for clinical reference only and are not the basis for diagnosis.