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VetScan Canine Ehrlichia Antibody Test Kit

This page contains information on VetScan Canine Ehrlichia Antibody Test Kit for veterinary use.
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  • VetScan Canine Ehrlichia Antibody Test Kit Indications
  • Warnings and cautions for VetScan Canine Ehrlichia Antibody Test Kit
  • Direction and dosage information for VetScan Canine Ehrlichia Antibody Test Kit

VetScan Canine Ehrlichia Antibody Test Kit

This treatment applies to the following species:
Manufacturer: Abaxis

FOR THE QUALITATIVE DETECTION OF ANTIBODIES TO EHRLICHIA CANIS, CHAFFEENSIS AND/OR EWINGII IN CANINE WHOLE BLOOD, PLASMA OR SERUM

For Veterinary Use Only

Intended Use

The VetScan Canine Ehrlichia Antibody Test Kit is a visual and rapid test for the qualitative detection of antibodies to E. canis, E. chaffeensis and/or E. ewingii in canine whole blood, serum or plasma. This test is for veterinary use only. Gram negative bacteria belonging to these Ehrlichia spp. are obligatory intracellular parasites and cause the disease known as Ehrlichiosis in man, dogs and some other animals. This disease is transmitted by a variety of tick species and has a world-wide distribution. Clinical signs of Ehrlichiosis differ in acute, sub-acute and chronic phases. The acute phase may be characterized by fever, anorexia, lethargy, lymphadenopathy and thrombocytopenia. Hypergammaglobulinemia (polyclonal or sometimes monoclonal gammopathy), thrombocytopenia and anemia are common occurrences in the sub-acute phase. Lethargy, weight loss, pancytopenia, bone marrow suppression and hemorhage eventually leading to death may occur in the chronic phase of Ehrlichiosis. Signs and symptoms as well as the outcome of disease may differ somewhat with the species of Ehrlichia causing the infection.

The VetScan Canine Ehrlichia Antibody Test Kit uses synthetic peptides that bind antibodies produced in dogs in response to certain dominant antigens of the above three Ehrlichia spp. Co-polymers of these synthetic peptides with bovine serum albumin are coated on colloidal gold particles and used in a double antigen sandwich assay to visualize the presence of antibodies binding to such peptides. The antibodies bound to antigen-coated gold particles flows through the strip and are captured by immobilized antigen on the test strip. The accumulation of the captured gold particle / antibody complex causes a color to become visible on the Test line (T). The intensity of the colored line is further enhanced by an amplification mechanism. A procedural Control line (C) will always appear whether the sample is positive or negative.

INSTRUCTION FOR USE

● This Test is for the detection of Ehrlichia spp. antibodies in canine samples.

● Refrigerated or frozen samples must be at room temperature 15° to 27°C (59° to 80°F) before running the assay-DO NOT HEAT.

● Whole canine blood collected in any type of EDTA, heparin, or citrate tubes may be used within one day of collection, provided no visual clotting has occurred. Do not freeze whole blood or use whole blood that has been frozen. If whole blood is not used within two hours of draw, store refrigerated.

● Serum or plasma, either fresh, previously frozen, or stored at 2° to 8°C (35° to 46°F), may be used in this test. Serum or plasma may be stored for use up to 7 days at 2° to 8°C (35° to 46°F). For longer storage, sample should be frozen at -20°C (-4°F) or colder.

● Previously frozen or older serum or plasma samples must be centrifuged at >1600g to remove any particulate material before use.

● Excessive hemolysis may obscure the results.

● EDTA, heparin, or ACID in plasma will not affect the results.

Precautions And Warnings

VetScan Canine Ehrlichia Antibody Test Kit Caution

Important: Do not remove device from the pouch until ready for use.

● Test Device must be used as soon as possible after removing from pouch and within a maximum of 15 minutes.

● For veterinary use only.

● Do not use components after expiration date.

● The Test Device should be used in a horizontal position on a flat surface while the test is performed. The Test Device should not be moved or tilted during the test procedure.

● Use a separate Transfer Pipette for each test.

● The Chase Buffer is not interchangeable from serial (lot) to serial (lot).

● Do not use a Test Device from a pouch that is obviously torn or damaged.

● Do not use a Test Device if it appears cracked, broken, or otherwise damaged.

● The Kit Components must not be frozen.

STORAGE

● The Test Devices and Chase Buffer must be stored at 2° to 27°C (35° to 80°F) and never frozen.

● Test Devices and Chase Buffer are stable until expiration when stored at recommended temperatures.

KIT COMPONENTS

1. Test Devices

2. Chase Buffer Bottle

3. Transfer Pipettes

4. Instruction for Use

TEST PROCEDURE

1. Remove the Test Device from the protective pouch and place on a flat surface. Label the Test Device with the patient I.D. or control identification.

2. Gently mix the sample by inverting.

3. Using the Transfer Pipette provided, transfer one drop of sample (whole blood, serum or plasma) in to the sample well.

4. Let the sample absorb for 30-60 seconds.

5. Holding the Chase Buffer Bottle vertically, add 3 drops of the chase buffer into the sample well. Read the results within 8-10 minutes. High positive results may appear as soon as 1 minute, and low positive results may take up to 8-10 minutes to appear. Do not read results after 15 minutes. Colored lines which appear after 15 minutes are not diagnostic and should be ignored.

INTERPRETATION OF TEST RESULTS

Positive Results

The test is positive if two colored lines appear. One colored line will appear at the Test line (T) area and other in the Control line (C) area. Any intensity of the Test line (T) should be considered positive. Colored lines may be lighter or darker than each other.

Negative Results

The result is negative if only one line appears at the Control line (C) area.

Invalid Results

The test is invalid if no colored line appears at the Control line (C) area even if a colored line appears at the Test line (T) area. Colored lines that appear after 15 minutes are not diagnostic and should be ignored.

EHRLICHIA TEST PROCEDURE

REFERENCES

T. Mark Neer, Edward B. Breitschwerdt, Russell T. Greene, and Michael R. Lappin (2002) Consensus Statement on Ehrlichial Disease of Small Animals from the Infectious Disease Study Group of the ACVIM. J Vet Intern Med. 16:309

Michael J. Day (2011) The Immunopathology of Canine Vector-Borne Diseases. Parasites & Vectors 2011, 4:48

READ ALL INSTRUCTIONS BEFORE BEGINNING THE ASSAY

Manufacturer

Abaxis, Inc., 3240 Whipple Road, Union City, CA 94587

800-822-2947

www.abaxis.com

Authorized Representative In The European Community

Abaxis Europe GmbH, Bunsenstr. 9-11, 64347 Griesheim, Germany

+49 6155 780 210

U.S. Veterinary License No. 424

For patent information, see www.abaxis.com/about_us/patents

510-7010 Rev. B

Presentation: 25 test kit.

CPN: 1740004.0

ABAXIS, INC.
3240 WHIPPLE ROAD, UNION CITY, CA, 94587
Telephone:   510-675-6500
Toll-Free:   800-822-2947
Fax:   510-441-6150
Website:   www.abaxis.com
Email:   abaxis@abaxis.com
Every effort has been made to ensure the accuracy of the VetScan Canine Ehrlichia Antibody Test Kit information published above. However, it remains the responsibility of the readers to familiarize themselves with the product information contained on the US product label or package insert.

Copyright © 2016 North American Compendiums. Updated: 2016-10-31

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