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IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic

IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic

Place of Origin:

CN

Brand Name:

WWHS

Certification:

CE

Model Number:

IL-6

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Product Details
Application:
Renal Injury
Type:
One Step Assay
Storage:
At Room Temperature
Feature:
High Sensitivity
Formal Name:
Interleukin-6
Reactivity:
Human
Throughput:
3000 Tests/Day
Sample:
WB / Serum / Plasma
Reaction Time:
10 Min.
Advantage:
High Accuracy
Payment & Shipping Terms
Minimum Order Quantity
1000
Price
Negotiable
Packaging Details
Colorful Paper Box
Delivery Time
7 Days
Payment Terms
T/T
Supply Ability
20000 Kits per Week
Product Description

【Product name】

Diagnostic Kit for Interleukin-6(Immunochromatographic assay)

 

【Packing specification】

25 Tests/kit

 

【Intended use】

The kit is used for quantitative determination of Interleukin-6 (IL-6) in human whole blood, plasma and serum.

Interleukin 6 is a member of the family of interleukins. It plays an important role in the inflammatory response and is a sensitive indicator for the early diagnosis of acute infection.

 

【Test principle】

The kit is a one-step chromatographic sandwich immunoassay designed for the quantitative measurement of IL-6. The IL-6 antigen in the sample was first bound with the conjugated compound of fluorescent labeled IL-6 monoclonal antibody, then moved and combined with another IL-6 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.

 

【Components】

Name Quantity Component
Test cards 25 It is composed of fluorescent pad (coated with fluorescently-labeled IL-6 monoclonal antibody), nitrocellulose membrane (coated with IL-6 monoclonal antibody and Goat anti mouse IgG antibody), absorbent paper and backing.
Sample diluent 25 (0.3mL/ tube) Phosphate buffer
ID card 1 With specific stand curve file

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

 

【Storage conditions and validity】

The kit should be stored at 4℃~30℃, out of direct sunlight. It is valid for 18 months. The test card should be used within 15 minutes after unsealing under the environment of 15℃~30℃ and 20% ~ 90% relative humidity.

The production date, batch number and expiration date are shown in the outer package of the product.

 

【Applicable instrument】

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

 

【Sample requirements】

  1. Plasma, serum and whole blood can be used as samples. The whole blood should be collected in a tube containing heparin, citrate or EDTA as the anticoagulant. If the serum procedure is used, collect blood in a tube without anticoagulant and allow clotting. Hemolyzed samples should not be used.
  2. Venous blood was collected according to routine laboratory methods to avoid hemolysis.
  3. It is highly recommended to use fresh samples instead of keeping the samples at room temperature for a long time. After samples were collected, the detection should be completed within 4 hours at room temperature (15℃~30℃). The whole blood sample can be stored at 2℃~8℃ for 24 hours. Plasma and serum samples can be stored at 2℃~ 8℃ for 7 days, -20℃ for 30 days.
  4. Before testing, the sample should return to room temperature (15℃~30℃). The frozen samples should be completely thawed, rewarming and mixed evenly before use. Repeated freeze-thaw cycles should be avoided.

 

【Test procedure】

  1. Before the test, please read the instructions completely. If the test card and sample are stored in cold storage, they should be balanced at room temperature (15-30)℃ for not less than 30min before use.
  2. Start NIR-1000 dry fluoroimmunoassay analyser according to the instruction manual of the instrument, and carry out quality control verification according to the instruction manual of the instrument(Note: the reagent has been calibrated in advance, and the calibration curve parameters of each batch of reagent have been stored in the ID card. The test can be carried out only after the quality control is passed. Otherwise, the cause should be found out before testing.)
  3. Remove the test card from the aluminum foil bag and use it within 15 minutes.
  4. Place the test card on a clean horizontal table and mark it horizontally.
  5. Mix 100 µL of patient sample with 300µL of sample diluent. Apply 100 µL of diluted samples to the well of the test card.
  6. Insert the test card into NIR-1000 dry fluoroimmunoassay analyser, read and record the results at 10 minutes after addition of samples, then dispose of used test appropriately.

 

【Reference interval】

The normal reference value is less than 10pg/mL in this assay. It is strongly recommended that each laboratory should determine its own normal and abnormal values.

 

【Interpretation of test results】

  1. This reagent is only used for auxiliary detection. If the test results are abnormal, it should be reviewed in time and judged in combination with clinical symptoms.
  2. For samples with IL-6 concentration lower than 5.00pg/mL and higher than 4000.00pg/mL, the detection results are reported as "<5.00pg/mL "and ">4000.00pg/mL ", respectively.

 

【Limitation of rest method】

  1. This kit is only used to detect human serum/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 30mg/mL, the content of hemoglobin shall not exceed 10mg/mL, and the content of bilirubin shall not exceed 0.25mg/mL, and the relative deviation of the test results shall not exceed ±15%.

4. When the concentration of IL-6 in the sample is less than 10000ng/mL, there is no hook effect.

  1. HAMA effect was not produced when the concentration of human anti rat in the sample was less than 50ng/ml.
  2. When RF concentration of samples is less than 2000IU/mL, relative deviation of test result is limited to ±15.0%.

 

【Performance】

1. Limits of detection

No higher than 5.00 pg/mL.

2. Accuracy

The relative deviation from the target value is limited to ±15.0%.

3. Repeatability

The within and between assay coefficient of variations are within 15.0%.

4. Linearity range

Within the linear range (5.00~ 4000.00)ng/mL, the linear correlation coefficient R≥0.990.

 

【Note】

1. The kit can be used for in vitro diagnosis only.

2. Test card and buffer solution are single-use and they 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. Take the test card out of the aluminum foil bag and carry out experiment in 15min. Do not place it in the air for a long time to avoid dampness.

5. It is required to strictly comply with the requirements for sample collection and storage. If the sample is turbid, please centrifuge and precipitate it before use.

6. The kit used should be disposed of as latent infective material, and all samples, reagents and latent contaminants should be disinfected and disposed of according to relevant local regulations.

 

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IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic 3IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic 4IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic 5IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic 6IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic 7IL-6 Rapid Test Kit IFA IVD CE FDA Medical Supply One Step PCR Antigen Rapid Diagnostic 8

 

About NIR-1000 Dry Fluoroimmunoassay Analyser

 

It is a fluorescence immunochromatographic analysing system with internal temperature control,

which can help diagnose conditions such as infection, diabetes, cardiovascular diseases, renal injury and cancers, etc.

Immunofluorescence technology

Testing time less than 15 minutes

Easy-to-use touch-screen platform,multi-language system

Reagents stored at room temperature for 12 months

 

Smarter Operation

 

1. High Quality: Imported Major Components with Advanced German Technology

2.User-Friendly Design: 7 Inch touch screen, great touch feeling, simple graphic interface

3. Built-In Lithium Battery: High Mobility for first aid&amulance

4. Two Test Mode: Internal&External mode for different clinical needs

5. Smart Report: Auto Printing

6. Visual Results: Able to connect with LIH/HIS

 

FAQ:

 

1. What is the MOQ?

 

Generally if you choose the different products, our minimum order qty. also will be different. One sample available.

 

2. What about the delivery time?

 

The goods need 7-21 work days to be made upon deposit.

 

3. What's your shipping method?

 

We provide comprehensive shipping methods.

 

For small quantity orders we ship by DHL Air-Express, or EMS/TNT/UPS/FEDEX Express service, it is safe and fast.

 

For large quantity orders we ship by Air transportation or sea transportation, we can also ship order to buyer’s cargo agent in China.

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