SE Ag

SE Ag

Product catalog summary
Storage and Handling Instructions:
  • The test device must be stored away from light at room temperature (4-30℃) and should not be frozen.
  • Use the test device before the expiration date on the package label.
Sample Collection Procedure:
  • Use a swab to collect fresh avian feces or a fecal sample from the rectum.
  • Insert the swab into the buffer or open the extraction tube containing the buffer and place it in the workstation.
  • Rotate the swab more than 10 times to ensure effective specimen collection.
Test Description:
  • The Salmonella Antigen Rapid Test is a lateral flow immunoassay for the qualitative detection of Salmonella (SE) antigen in fresh feces or rectal swab samples.
  • It is intended for avian use only and helps determine SE infection.
Precautions:
  • Humidity and temperature may influence results.
  • Ensure the foil pouch is undamaged before opening and perform the test immediately after opening.
  • Do not reuse test components or use them after the expiry date.
  • Do not mix components from different lot numbers.
  • Wear protective gloves when handling samples and wash hands thoroughly afterward.
  • Decontaminate and dispose of all samples, used kits, and potentially contaminated materials safely according to regulations.
Test Components:
  • Test devices, swabs, extraction tubes, disposable droppers, package insert, and workstation.
Testing Procedure:
  • Ensure the test operation is at room temperature (15–30 ℃).
  • Place the test device on a clean, flat surface, open the extraction tube cap, and use a dropper to add three drops (about 90 μL) of the mixed sample into the specimen well (S) of the test device.
Interpretation of Results:
  • Negative (-): Only a clear C line appears.
  • Positive (+): Both C line and T line appear, regardless of T line intensity.
  • Invalid: No colored line appears in the C region, regardless of T line appearance.
Additional Notes:
  • While the test is accurate, false results may occur. Further clinical or laboratory tests may be required for questionable results.
  • A definitive diagnosis should not be based solely on this test but should be made by a veterinarian after evaluating all clinical and laboratory findings.
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Catalog excerpts

SE Ag-1

Salmonella Antigen Rapid Test(SE Ag) Intended Use Salmonella Antigen Rapid Test is a lateral flow immunoassay intended for the qualitative detection of specific antigen from Salmonella (SE) in fresh feces or rectal swab sample. The test is useful for determination of SE infection. Reagent and Materials Provided • Test devices • Extraction tubes • Disposable droppers ■ Package insert • Workstation Materials Required but not Provided The test device is sealed and should be stored away from light at a room temperature (4-30C). Do not freeze. The test device should be used before the expiration date marked on the package label. Warnings, Precautions and Safety Information 1. The test device is used for avian only. 2. The results may be influenced by humidity and temperature 3. Make sure that the foil pouch containing the test is not damaged before open. Perform the test immediately when the pouch package is opened. 4. Do not reuse the test components. 5. Do not use after the expiry date. 6. Do not mix product components in different lot numbers 7. As all samples are potentially infectious. Operators should wear protective gloves while handling samples and wash hands thoroughly afterwards. 8. Decontaminate and dispose of all samples, used kits and potentially contaminated materials safely in accordance with national and local regulations. STEP 1 CHECK THE KIT CONTENTS BEFORE USE Test device Swab Disposable Extraction Package Workstation dropper tube insert Check the product contents and make sure the test operation is under the room temperature (15—30 C) before testing. STEP 2 TEST PROCEDURE Open the cap of the extraction Place the extraction tube tube containing the buffer. in the workstation. Use the swab to collect some fresh avian feces or fecal sample from its rectum. And then put the swab into the buffer. Rotate the swab more than 10 times and make sure the specimen is effectively collected. Take the test device out of the aluminum foil bag, and place it on a clean, flat table. Open the cap of the extraction tube. Use a dropper to draw some mixed sample and add three drops (about 90 pL) vertically into the specimen well (S) of the test device. STEP 3 INTERPRETATION OF TEST RESULT Read the result at 5-10 minutes. The result is invalid after 15 minutes. Positive (+): The presence of both C line and T line, regardless of T line being strong or faint. Negative (-): Only clear C line appears. Invalid: No colored line appears in C region, regardless of T line’s appearance. Although the Salmonella Antigen Rapid Test is very accurate in detecting Salmonella Antigen, a low incidence of false results may be occurred. Other clinically or laboratory tests might be required if questionable results are obtained. As other diagnostic tests, a definitive clinical diagnosis should not be based on the result of a single test, but should be diagnosed by the veterinarian after all clinical and laboratory findings have been evaluated. | |VD | in vitro diagnotic medical device temperature limitation OS contains sufficient for <n> tests ml Hangzhou Antlgenne Technology Co., Ltd Address: Block A, Building 3, No. 8, Xiyuan 9th Road, Xihu District, Hangzhou, Zhejiang, 310030 P.R. China

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