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FERR Real Time PCR Kits FIA IVD Rapid Quantitative Test Kit By NIR-1000

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FERR Real Time PCR Kits FIA IVD Rapid Quantitative Test Kit By NIR-1000

Country/Region china
City & Province shenzhen
Categories Incontinence Care
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Product Details

【Product name】 FERR.pdf

Diagnostic Kit for Serum Ferritin(Immunochromatographic assay)

 

 

【Intended use】

It is used to quantitatively detect the content of ferritin in human serum. Clinically, it is mainly used for the auxiliary diagnosis of iron metabolism related diseases, such as hemochromatosis and iron deficiency anemia.

 

【Test principle】

The principle of immunofluorescence chromatography was applied to the kit. The Ferr antigen in the sample was first bound with the conjugated compound of fluorescent labeled Ferr monoclonal antibody, then moved and combined with another Ferr monoclonal antibody fixed on the nitrocellulose membrane, and the double antibody sandwich complex was formed at the detection line of the cellulose nitrate membrane. The quantitative detection results were obtained by NIR-1000 dry fluoroimmunoassay analyser.

 

【Main components】

It is composed of fluorescent pad (coated with fluorescent labeled Ferr monoclonal antibody), nitrocellulose membrane (coated with Ferr monoclonal antibody and Goat anti mouse IgG antibody), absorbent paper and backing

The components in different batches of kits cannot be used interchangeably.

 

【Applicable instruments】

NIR-1000 dry fluoroimmunoassay analyser produced by WWHS Biotech. Inc.

 

【Sample requirements】

  1. The sample types of this product are EDTA·K2 anticoagulant plasma, EDTA·Na2 anticoagulant plasma, sodium citrate (anticoagulant tube with the ratio of sodium citrate volume to blood collection volume of 1:9), EDTA·K2 anticoagulant whole blood, EDTA·Na2 anticoagulant whole blood and sodium citrate (anticoagulant tube with the ratio of sodium citrate volume to blood collection volume of 1:9).
  2. Venous blood was collected according to routine laboratory methods to avoid hemolysis.
  3. After clinical samples were collected, the detection was completed within 4 hours at room temperature (15℃~30℃). The whole blood sample can be stored for 24 hours at 2℃~8℃; Plasma samples can be stored at 2℃ to 8℃ for 7 days; The plasma sample was at - 20℃. It can be stored for 30 days at room temperature.
  4. Before testing, the sample must return to room temperature (15℃~30℃). The frozen samples should be completely thawed, rewarming and mixed evenly before use, and repeated freezing and thawing should be avoided.

 

【Reference interval】

Through the determination of serum samples from 301 healthy people aged 10 ~ 87, the results were statistically analyzed.

Gender

2.5th

(ng/mL)

97.5 percentile

(ng/mL)

Male24335
Female11307

 

 

【Limitations of methods】

  1. This kit is only used to detect human plasma/whole blood samples
  2. Due to the limitations of immunoassay methods of antigen and antibody reaction, the results cannot be used as the only basis for clinical diagnosis, but should be evaluated with all the existing clinical and experimental data.
  3. The content of triglyceride in the sample shall not exceed 15mg/ml, the content of hemoglobin shall not exceed 5mg/ml, and the content of bilirubin shall not exceed 0.5mg/ml, and the relative deviation of the test results shall not exceed ±15%.
  4. When the concentration of Ferr in the sample is less than 1000ng/ml, there is no hook effect.
  5. HAMA effect was not produced when the concentration of human anti rat in the sample was less than 50ng/ml.
  6. When RF concentration in the sample is less than 2000IU/ml, the relative deviation of the test results is within ±15%.

【Note】

1. This kit is only used for in vitro diagnosis.

2. The test card and sample diluent are disposable and cannot be reused.

3. Please check the integrity and validity of the kit package before use, and then open the package. When it is stored at low temperature, it should be restored to room temperature (15℃~30℃) before opening the package for use. The reagents with damaged inner package and beyond the validity period cannot be used.

4. The requirements of specimen collection and storage should be strictly observed. If the specimen is turbid, it should be centrifuged and discarded before use.

5. The used kits should be treated as potential infectious substances, and all samples, reagents and potential pollutants should be disinfected and treated according to the relevant local regulations.

 

 

 

cat#.Product ItemSpecimenReaction TimeMeasure RangeClinical RangeIntended Use
47FERRSerum5min.10-500ng/mlMale:24ng/mL~335ng/mL,
Female:11ng/mL~307ng/mL
iron metabolism related diseases, such as hemochromatosis and iron deficiency anemia

 

 

 

 

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