Filariasis IgG/IgM Test Card
Filariasis IgG/IgM Test Card (丝虫病IGG/IgM检测试纸卡) is a one-step qualitative lateral flow rapid diagnostic test kit, based on the Colloidal Gold Chromatographic Immuno Indirect principle, which is used to detect Filariasis IgG/IgM Antibodies in human Serum, Whole Blood or Plasma specimen.
Please refer to the Instruction for Use (IFU) of the Filariasis IgG/IgM Test Card. (For reference only; Read the package insert in the test kit before performing any test.)
Detailed information of Filariasis IgG/IgM Test Card
- General and Technical information of this FILA test kit;
- Packing specification of this FILA Card style test kit (gross weight in full kit package and in bulk packing);
- Specimen used to carry out the assay, and the requirements on specimen collection, storage and processing; and,
- Specific immuno assay principle used in this Filariasis Test Kit.
Main technical information of this Filariasis IgG/IgM test kit is listed in the following table:
|Catalog No.:||FILA 461|
|Description:||Filariasis IgG/IgM Test Card|
|Category:||Arthropod Borne Disease|
|Specimen:||Serum, WB, Plasma|
|No. of Step:||One Step|
|Reading Time:||15 Minutes|
|Quan. or Qual.:||Qualitative|
|Assay Principle:||Colloidal Gold Chromatographic Immuno Indirect|
The standard kit size of this Filariasis Card test kit is 25 tests per box; 40 boxes per carton.
To save freight cost, sometimes bulk packing is used, meaning test strip, cassette or multi-test panel is packed in single aluminum pouch; 50 or 100 pouches in one plastic bag; and then plastic bags are packed in cartons along with the unfolded boxes for the test kits. In this way, the customers can easily pack the tests into test kits after receiving the bulk packed goods.
|Tests per Kit:||25 Tests|
|Dimension of Kit Box:||21.0 * 12.5 * 6.5 CM|
|Boxes per Carton:||40 Kits|
|Tests per Carton (BULK):||1600 Tests|
|G.W. per Carton (Boxed):||14.0 KG|
|G.W. per Carton (Bulk):||16.5 KG|
|Carton Dimension:||53 * 45 * 36 CM|
|Carton Volume:||0.085 CBM|
- Test cassette in single foil pouch with desiccant;
- Disposable sample dropper;
- Specimen Diluents;
- Instruction leaflet.
To carry out the assay with a Filariasis IgG/IgM Test Card, Serum, WB or Plasma should be collected according to the instructions given in the Instruction For Use included in the test kit. After collecting, it is preferable to perform the testing as early as possible; if not viable, the specimen should be stored properly. A general introduction about the collection, and storage of the specimens is given below.
Collect blood specimen into a red top blood collection tube by vein puncture, which contains no anticoagulants.
Allow the blood to clot, or separate the serum by centrifugation.
Carefully withdraw the serum into a new pre-labeled tube.
Whole Blood Collection
Whole blood can be collected with blood collection tube with venipuncture into blood collection tube (containing EDTA, citrate or heparin).
Or, by lancet lancing. Clean the area to be lanced with an alcohol swab. Squeeze the end of the fingertip and pierce with a sterile lancet. Wipe away the first drop of blood with sterile gauze or cotton. Take a dropper provided, while gently squeezing the dropper tube, immerse the open end in the blood drop and then gently release the pressure to draw blood into the dropper.
Collect blood specimen into a lavender, blue or green top blood collection tube, containing EDTA, citrate or heparin, respectively, by vein puncture.
Separate the plasma by centrifugation.
Carefully withdraw the plasma into a new pre-labeled tube.
Serum, WB, Plasma Storage Condition
Test specimens as soon as possible after collecting.
The specimens can be stored up to 3 days at 2-8°C if not tested immediately. The specimens should be frozen at -20°C for longer time storage. Don’t freeze and thaw the specimens for many times.
Prior to testing, bring frozen specimens to room temperature slowly and mix gently.
Specimens containing visible particulate matter should be clarified by centrifugation before testing.
Do not use samples demonstrating gross lipemia, gross hemolysis or turbidity in order to avoid interference on result interpretation.
Colloidal Gold Chromatographic Immuno Indirect method is used in this Filariasis IgG/IgM Test Card to detect the Filariasis IgG/IgM Antibodies in human Serum, WB or Plasma specifically. The introduction of this Colloidal Gold Chromatographic Immuno Indirect testing principle is given blow.
In the lateral flow indirect chromatographic rapid test, recombinant or purified antigens are immobilized in the test band region. In the end of the Conjugate pad of the membrane strip where the samples are supposed to be added, rabbit or mouse anti-human IgG antibodies conjugated with colloidal gold particles is embedded.
During the testing process, specimen is added to the end of the membrane strip. anti-IgG colloidal gold particles resolve into the specimen, where the anti-IgG conjugate will react and bound with the target IgG antibody, if present.
This complex of IgG and anti-IgG will move along the membrane strip to the testing band region, under capillary effect, where the immobilized antigen captures the IgG antibody. When the antigen-IgG-Anti-IgG complex accumulate on the test band region, the congregated colloidal gold particle will develop red or pink color, indicating there are target IgG antibodies in the specimen.
If there is no target IgG antibody in the specimen, the secondary anti-IgG conjugate will not bind to the immobilized antigen in the test band region, and no color will develop.
As a procedural quality control, a secondary antibody or recombinant antigen will be immobilized in the control band region. When the specimen climb to this region, the unbound anti-IgG colloidal gold particle will be captured, thus a red band will always develop. This inner control process ensure that enough specimen is added, proper testing procedure has been followed, and the reagent has not deteriorated.