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PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved

WWHS Biotech.Inc(exclusive marketed by Dawin)
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    Buy cheap PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved from wholesalers
     
    Buy cheap PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved from wholesalers
    • Buy cheap PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved from wholesalers
    • Buy cheap PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved from wholesalers
    • Buy cheap PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved from wholesalers
    • Buy cheap PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved from wholesalers

    PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved

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    Brand Name : WWHS
    Certification : ISO 13485, CE
    Price : Negotiable
    Payment Terms : L/C, T/T
    Supply Ability : 20000 Kits per Week
    Delivery Time : 7 Days
    Model Number : D-Dimer
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    PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved

    【Product name】

    D-Dimer Rapid Quantitative Test(Fluorescence immunoassay)

    【Package specification】

    20 Tests/box

    【Intended use】

    This kit is used for quantitative determination of D-dimer in human whole blood and plasma.

    【Inspection principle】

    The principle of immunofluorescence chromatography was applied to the kit. The D-dimer antigen in the sample was first bound with the conjugated compound of fluorescent labeled D-dimer monoclonal antibody, then moved and combined with another D-dimer 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】

    NameQuantityComponent
    Test card25It is composed of fluorescent pad (coated with fluorescent labeled D-dimer monoclonal mouse antibody), nitrocellulose membrane (coated with D-dimer monoclonal mouse antibody and Goat anti mouse IgG antibody), absorbent paper and backing
    Sample buffer25(300μL/tube)Phosphate buffer
    ID card1Record the standard curve information of this kit

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

    【Storage conditions and validity】

    The test card should be stored at 4℃~30℃, dry, dark and no freezing. It should be stored in sealed aluminum foil bag and valid for 12 months. The test card should be returned to room temperature (15℃~30℃) before opening. It 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 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.

    【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 information card. The information card is inserted before use, so it is not necessary to calibrate again, and 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 10 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, press the [timing detection] key, automatically time for 10 minutes, automatically judge the test results, and display the quantitative results on the screen. Or insert the test card into the analyzer after timing for 10 minutes, and press the [real time detection] key, and the instrument will automatically interpret the test results.

    【Reference interval】

    By measuring 268 healthy people aged between 19 and 79, statistical analysis shows that the reference interval is less than 500 ng/ml. According to the characteristics of the local population, the reference intervals of the laboratories were established.

    【Interpretation of 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 D-dimer concentration lower than 40ng/ml and higher than 10000ng/ml, the detection results are reported as "< 40ng/ml" and "> 10000ng /ml", respectively.

    【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 D-dimer in the sample is less than 20000ng/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%.

    【Performance】

    1. Analysis sensitivity

    No more than 40ng/ml.

    2. Accuracy

    The relative deviation from the target value is within ±15%.

    3. Precision

    The within and between assay coefficient of variations are within 15%.

    4. Linear range

    Within the linear range (40 ~ 10000ng/ml), the linear correlation coefficient R≥0.990.

    【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.

    PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved


    WWHS Assay list     
    Cardiac     
    cat#.Product itemSpecimenReaction TimeMeasure RangeClinical RangeItended Use
    1cTnIWB/Serum/Plasma12min.0.1-40ng/ml<0.3ng/mlseveral heart diseases including myocardial infarction and heart failure.
    2MyoWB/Serum/Plasma12min.5-400ng/ml<58ng/mlacute myocardial infarction (AMI) in early stage.
    3CK-MBWB/Serum/Plasma12min.1-200ng/ml<5ng/mlacute myocardial infarction (AMI) in early stage.
    4NT-proBNPWB/Serum/Plasma10min.20-35000pg/mlUnder 75:0~347pg/mL,
    Over 75:0~449pg/mL
    heart failure .
    5D-DimerWB/Plasma10min.40-10000ng/ml<500ng/mldisseminated intravascular coagulation (DIC),deep vein thrombosis (DVT),pulmonary embolism (PE), myocardial infarction, cerebral infarction, etc.
    6cTnI+Myo+CKMBWB/Serum/Plasma12min.same with single itemsame with single itemTriple marker of myocardial infarction.
    7ST2WB/Serum/Plasma10min.10-400ng/ml<35ng/mlheart failure .
    8Lp-PLA2WB/Serum/Plasma10min.10-900ng/ml<175ng/mlRisk evaluation of ACS and atherosclerotic ischemic stroke patients.
    9S100-βWB/Serum/Plasma10min.0.05-10ng/ml<0.2ng/mlCerebral infarction, cerebral injury.
    Inflammation     
    10CRP / hs-CRPWB/Serum/Plasma3min.0.5-200mg/LCRP<10mg/L,hs-CRP<1mg/Lnonspecficity inflammatory marker.
    11SAASerum5min.1-200mg/L<10mg/Linflammation&infection.
    12PCTWB/Serum/Plasma10min.0.2-100ng/ml<0.5ng/mlSepsis
    13CRP+SAAWB/Serum/Plasma5min.same with single itemsame with single iteminflammation&infection.
    14IL-6WB/Serum/Plasma10min.5-4000pg/ml10pg/mldiabetes,rheumatoid arthritis,etc
    Thyroid Hormone     
    15TSHSerum/Plasma15min.0.3-100mU/L0.35-5mU/Lhyperthyroidism and hypothyroidism
    16TT3Serum/Plasma15min.0.5-10nmol/L1.3-3.1nmol/Lthyroid dysfunction
    17TT4Serum/Plasma15min.5-300nmol/L66-181nmol/Lthyroid dysfunction
    18FT3Serum/Plasma15min.1-100pmol/L4-10pmol/Lthyroid dysfunction
    19FT4Serum/Plasma15min.5-300pmol/L19-39pmol/Lthyroid dysfunction
    Tumor Marker     
    20AFPSerum/Plasma15min.2.5-200ng/ml<20ng/mlpregnancy cancer
    21CEASerum/Plasma15min.1-200ng/ml<5ng/mlcolon cancer, colorectal cancer,etc.
    22NSESerum/Plasma15min.1-400ng/ml<16ng/mlnon-small cell lung cancer
    23FOBfecal specimens10min.50-1000ng/ml<100ng/mlAbnormal recessive gastrointestinal bleeding
    24PG IISerum/Plasma15min.1-100ug/LPGI/PGII>3.0gastric abnormalities
    25PG ISerum/Plasma15min.2.5-200ug/L>70ng/mlgastric abnormalities
    26TPSASerum/Plasma15min.0.5-40ng/ml<4ng/mlprostate cancer
    27FPSASerum/Plasma15min.0.1-10ng/ml<1ng/mlprostate cancer
    28CA12-5Serum/Plasma15min.20-500U/ml<35U/mlovarian cancer
    29CA15-3Serum/Plasma15min.10-400U/ml< 25 U/mLbreast cancer
    30HE4Serum/Plasma15min.50-2000pmol/L<140 pmol/Lovarian cancer
    31CA19-9Serum/Plasma15min.10-400U/ml< 27 U/mLpancreatic cancer
    32β-HCGSerum/Plasma15min.5-400mIU/ml<10 mIU/mLEarly pregrancy, ectopic HCG cancer,incomplete abortion
    33CK19(Cyfra21-1)Serum/Plasma15min.0.5-50ng/ml<2.5ng/mlnon-small cell lung cancer
    Fertility     
    34HCG / β-HCGSerum/Plasma10min.5-20000mIU/ml<5 mIU/mLearly pregrancy.
    35AMHSerum/Plasma10min.0.1-16ng/mlMale: 20-60 years old, 0.92-13.89 ng/mL
    Female: 20-29 years old, 0.88-10.35 ng/mL
    30-39 years old, 0.31-7.86 ng/mL 40 -50 years old, <5. 07 ng/mL
    ovarian reserve level
    Gastrointestinal      
    36FOBfecal specimens10min.qualitativequalitativegastrointestinal hemorrhage.
    37TRFfecal specimens10min.qualitativequalitativegastrointestinal hemorrhage.
    38FOB+TRFfecal specimens10min.qualitativequalitativegastrointestinal hemorrhage.
    Infection      
    39C.PneumoniaWB/Serum/Plasma15min.qualitativequalitativeCP infection
    40M.PneumoniaWB/Serum/Plasma15min.qualitativequalitativeMP infection
    41Covid-19 Antigennasal swab, throat swab or nasal wash/aspirate specimens15min.qualitativequalitativerespiratory tract
    42Covid-19 Ab IgG/IgMWB/Serum/Plasma15min.qualitativequalitativerespiratory tract
    43FluAnasal swab, throat swab or nasal wash/aspirate specimens15min.qualitativequalitativerespiratory tract
    44FluBnasal swab, throat swab or nasal wash/aspirate specimens15min.qualitativequalitativerespiratory tract
    Renal Injury      
    45CysCWB/Serum/Plasma5min.0.4-9mg/L0.5-1.1mg/Lrenal function
    46NGALUrine10min.10-1500ng/mL<132ng/mLacute kidney injury.
    Other      
    47FERRSerum5min.10-500ng/mlMale:24ng/mL~335ng/mL,
    Female:11ng/mL~307ng/mL
    iron metabolism related diseases, such as hemochromatosis and iron deficiency anemia
    48HbA1cWB10min.4%-14%4%-6%diabetes
    49VDSerum/Plasma15min.8-70ng/mL19-57ng/mLfetation

    Interpretation of Test Results


    1. The kit can be used for auxiliary test only. If test result is abnormal, retest timely and judge combined with clinical symptoms.
    2. For samples whose cTnI concentration is lower than 0.1ng/mL and higher than 40ng/mL, test result is “<0.1ng/mL” and “>40ng/mL” respectively.


    Note:


    1) Any variation in operator, pipetting and washing technique, incubation time or temperature, and kit age can cause variation in
    result. Each user should obtain their own standard curve.
    2) If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.
    3) If specimens generate values higher than the highest standard, dilute the specimens and repeat the assay


    FAQ


    Q1: Are you trading company or manufacturer ?
    A1: We are manufacturer.


    Q2: Do you provide samples ?
    A2: Yes,we do provide samples.If you need it, please contact us.


    Q3: How about the quality?
    A3: We have the best professional engineer and strict QA and QC system to ensure you get high quality products from us.


    Q4: How’s the package?
    A4: Normally are cartons, but also we can pack it according to your requirements.


    Q5: How’s the delivery time?
    A5: It depends on the quantity you need.

    Quality PCR Rapid Cardiac Testing Kit FIA Real Time For D-Dimer ISO 13485 Approved for sale
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