Leishmania Ab Test
INTENDED USE
Leishmania Ab Rapid Test is a sandwich lateral flow immunochromatographic assay for the qualitative detection of leishmania antibody (LSH Ab) in dog’s serum or plasma.
Assay Time: 5-10 min
Sample: Serum or plasma.
PRINCIPLE OF THE ASSAY
Leishmania Ab Rapid 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 leishmania antibodies 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 leishmania antibodies in the sample.
KIT COMPONENT
- 10×foil pouches, each containing a cassette, pipette and desiccant
- 10×assay buffer tubes (0.5 mL each)
- 10×centrifugal tubes
- Product Manual
PRECAUTIONS
- For best results, please strictly adhere to these instructions.
- All reagents must be at room temperature before running the assay.
- Do not remove test cassette from its pouch until immediately before use.
- Do not reuse the test kit.
- Do not use the test beyond its expiration date marked on the foil pouch.
- The components in this kit have been quality control tested as standard batch unit. Do not mix components from different lot numbers.
LIMITATION
Leishmania 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 IFA for final determination in practice.
Nico Lee
Product Manager
Skype: live:nico_5218
Tel: +86(755)89589611
Fax: +86(755)89580096
Email: nico@spanbio.com
Web:
中文
