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High Precision LT C4 Mouse ELISA Kit 20ng/L - 6000ng/L Standard Curve Range

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    Buy cheap High Precision LT C4 Mouse ELISA Kit 20ng/L - 6000ng/L Standard Curve Range from wholesalers
     
    Buy cheap High Precision LT C4 Mouse ELISA Kit 20ng/L - 6000ng/L Standard Curve Range from wholesalers
    • Buy cheap High Precision LT C4 Mouse ELISA Kit 20ng/L - 6000ng/L Standard Curve Range from wholesalers

    High Precision LT C4 Mouse ELISA Kit 20ng/L - 6000ng/L Standard Curve Range

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    Brand Name : BT Lab
    Model Number : Cat.No E0498Mo
    Certification : CE, ISO9001:2005, MSDS
    Price : Negotiation
    Supply Ability : Western Union, T/T
    Delivery Time : 1-3 business days, bulk order within one week
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    High Precision LT C4 Mouse ELISA Kit 20ng/L - 6000ng/L Standard Curve Range

    High Precision and Sensitivity Mouse LT C4 ELISA Kit For Accurate Quantitative Detection


    Cat.No E0498Mo

    *This product is for research use only, not for use in diagnosis procedures. It’s highly recommend to read this instruction entirely before use.


    Intended Use

    This sandwich kit is for the accurate quantitative detection of Mouse Leukotriene C4 (also known as LT-C4) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.


    Reagent Provided

    ComponentsQuantity
    Standard Solution (8000ng/L)0.5ml x1
    Pre-coated ELISA Plate12 * 8 well strips x1
    Standard Diluent3ml x1
    Streptavidin-HRP6ml x1
    Stop Solution6ml x1
    Substrate Solution A6ml x1
    Substrate Solution B6ml x1
    Wash Buffer Concentrate (30x)20ml x1
    Biotinylated Mouse LT-C4 Antibody1ml x1
    User Instruction1
    Plate Sealer2 pics
    Zipper bag1 pic

    Material Required But Not Supplied

    • 37°C±0.5°C incubator
    • Absorbent paper
    • Precision pipettes and disposable pipette tips
    • Clean tubes
    • Deionized or distilled water
    • Microplate reader with 450 ± 10nm wavelength filter

    Precautions

    • Prior to use, the kit and sample should be warmed naturally to room temperature 30 minutes.
    • This instruction must be strictly followed in the experiment.
    • Once the desired number of strips has been removed, immediately reseal the bag to protect the remain from deterioration. Cover all reagents when not in use.
    • Make sure pipetting order and rate of addition from well-to-well when pipetting reagents.
    • Pipette tips and plate sealer in hand should be clean and disposable to avoid cross-contamination.
    • Avoid using the reagents from different batches together.
    • Substrate solution B is sensitive to light, don’t expose substrate solution B to light for a long time.
    • Stop solution contains acid. Please wear eye, hand and skin protection when using this material. Avoid contact of skin or mucous membranes with kit reagent.
    • The kit should not be used beyond the expiration date.

    Specimen Collection

    Serum Allow serum to clot for 10-20 minutes at room temperature. Centrifuge at 2000-3000 RPM for 20 minutes.


    Plasma Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 15 minutes at 2000-3000 RPM at 2 - 8°C within 30 minutes of collection.


    Urine Collect by sterile tube. Centrifuge at 2000-3000 RPM for approximately 20 minutes. When collecting pleuroperitoneal fluid and cerebrospinal fluid, please follow the procedures above-mentioned.


    Cell Culture Supernatant Collect by sterile tubes when examining secrete components. Centrifuge at 2000-3000 RPM for approximately 20 minutes. Collect the supernatants carefully. When examining the components within the cell, use PBS (pH 7.2-7.4) to dilute cell suspension to the cell concentration of approximately 1 million/ml. Damage cells through repeated freeze-thaw cycles to let out the inside components. Centrifuge at 2000-3000 RPM for approximately 20 minutes.


    Tissue Rinse tissues in PBS (pH 7.4) to remove excess blood thoroughly and weigh before homogenization. Mince tissues and homogenize them in PBS (pH7.4) with a glass homogenizer on ice. Thaw at 2-8°C or freeze at -20°C. Centrifuge at 2000-3000 RPM for approximately 20 minutes.


    Summary

    1. Prepare all reagents, samples and standards.

    2. Add sample and ELISA reagent into each well. Incubate for 1 hour at 37°C.

    3. Wash the plate 5 times.

    4. Add substrate solution A and B. Incubate for 10 minutes at 37°C.

    5. Add stop solution and color develops.

    6. Read the OD value within 10 minutes.


    Calculation of Result

    Construct a standard curve by plotting the average OD for each standard on the vertical (Y) axis against the concentration on the horizontal (X) axis and draw a best fit curve through the points on the graph. These calculations can be best performed with computer-based curve-fitting software and the best fit line can be determined by regression analysis.


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