1. Principle
This test kit is based on the competitive enzyme immunoassay for the detection of Florfenicol in the tissue (chicken,pork), fish, shrimp , honey. The coupling antigen is pre-coated on the micro-well stripes. The Florfenicol in the testing sample competes with the coupling antigen pre-coated on the micro-well stripes for the antibody against Florfenicol. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the testing sample has a negative correlation with the content of Florfenicol in it. This value is compared to the standard curve and the content of the corresponding Florfenicol is subsequently obtained.
2. Technical specifications
Sensitivity : 0.5ppb
Detection limit:
Honey1.5ppb
Meat,liver,shrimp ,fish0.5ppb
Recovery rate
Honey70%10%
Meat,liver,shrimp ,fish80%10%
Cross-reaction rate:
Florfenicol100%
Thiamphenicol¼T0.1%
Chloramphenicol¼T0.1%
96 wells
H-fabp fast test kit (immunofluorescence assay) is intended for use together with getein1100 immunofluorescence quantitative analyzer (getein1100) or getein1600 immunofluorescence quantitative analyzer (getein1600) to quantitatively determine the concentrations of h-fabp in human serum, plasma, or whole blood specimens in point-of care and laboratory settings. H-fabp fast test kit (immunofluorescence assay) is intended for in vitro quantitative determination of heart-type fatty acid binding protein (h-fabp) in serum, plasma or whole blood. This test is used in the early diagnosis of ami and pulmonary embolism, and monitoring of chronic heart failure.
Intended use: Toxoplasma IGG/IGM rapid test is a rapid immunochromatographic test for the simultaneous detection of IGM and IGG antibodies to toxoplasma gondii in human serum/plasma. The test can be used as a screening test for toxoplasma infection and as an aid for differential diagnosis of the self limiting primary toxoplasma infections and the potentially fatal secondary toxoplasma infections in conjunction with other criteria. Test principle: The toxoplasma IGG/IGM rapid test is a lateral flow chromatographic immunoassay. The test cassette consists of: 1) A burgundy colored conjugate pad containing toxoplasma recombinant envelope antigens conjugated with colloid gold (toxoplasma conjugates) and rabbit igg-gold conjugates, 2) A nitrocellulose membrane strip containing two test bands (t1 and t2 bands) and a control band (c band). The t1 band is pre-coated with the antibody for the detection of IGM anti-toxoplasma, t2 band is coated with antibody for the detection of igg anti-toxoplasma, and the c band is pre-coated with goat anti rabbit IGG. Absence of any t bands (t1 and t2) suggests a negative result. The test contains an internal control (c band) which should exhibit a burgundy colored band of the immunocomplex of goat anti rabbit igg/rabbit igg-gold conjugate regardless of the color development on any of the t bands. Otherwise, the test result is invalid and the specimen must be retested with another device. Reagents and materials supplied : 1. Test cassette individually foil pouched with a desiccant. 2. Plastic dropper 3. Buffer 4. Package insert. Storage and stability: The kit must be stored at 2-30pc. Warning and precautions: 1. For in vitro diagnostic use only. Not for medicinal use. 2. Do not use beyond expiry date. 3. Read the instructions careful y before performing the test. 4. Handle all specimen as potential y infectious. 5. Follow standard biosafety guidelines for handling and disposal of potential y infective material.
1. Principle This test kit is based on the competitive enzyme immunoassay for the detection of Clenbuterol in the pork. The coupling antigen is pre-coated on the micro-well stripes. The Clenbuterol in the testing sample competes with the coupling antigens pre-coated on the micro-well stripes for the antibodies against Clenbuterol. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the testing sample has a negative correlation with the content of Clenbuterol in it. This value is compared to the standard curve and the content of the corresponding Clenbuterol is subsequently obtained. 2. Technical specifications Sensitivity : 0.1 ppb Detection limit: Tissue0.1ppb Urine, serum0.1ppb Feed50 ppb Recovery rate Urine, serum9010% Tissue8010% Feed8015% Cross-reaction rate: Clenbuterol100% Terbutalin< 1% Salbutamal< 19% Ractopamine< 1% 96 well
We have just achieved a major breakthrough in the development of dengue igg/igm antibody early test. Our new product is capable to detect the presence of dengue igm antibody in human serum within 3-5 days since primary infection (tested and verified with reference standard blood sample from usa cdc), while similar products currently found on the market can only detect it after at least 10-15 days. The significance of this achievement is that the new dengue igg/igm antibody early test now can diagnose dengue infection at a very early stage, which previously could only be done with a dengue ns1 antigen test. Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Sensitivity: 95.3% Specificity: 95.0% Specimen: whole blood/serum/plasma .
Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Sensitivity: 94.3% Specificity: >98.9% Specimen: whole blood/serum/plasma .
Highest accuracy Fast result interpretation Cost effective Made with best choices of materials Type: immunoassay system Brand name: ntbio/oem/private label Place of origin: british columbia, canada Size: 60mm x 300mm Cut-off value: 1000 ng/ml Sensitivity: 99.5% Specificity: >99.7% Specimen: urine .
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