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Mouse Retn Resistin Elisa Kit 96 Wells 2 - 8°c Storage With High Precision

Categories Mouse ELISA Kit
Brand Name: BT Lab
Model Number: Cat.No E0263Mo
Certification: CE, ISO9001:2005, MSDS
Place of Origin: Shanghai, China
MOQ: Negotiation
Price: Negotiation
Payment Terms: Western Union, T/T
Supply Ability: In Stock
Delivery Time: 1-3 business days, bulk order within one week
Packaging Details: Wrapped with ice pack and styrofoam package
Known as: Retn
Lead Time: Within 48 hours
Sample: serum,plasma,urine,tissue,cell culture supernatant
Shipping: DHL/FedEX
Storage: 2-8°C
Organism Species: mouse
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    Mouse Retn Resistin Elisa Kit 96 Wells 2 - 8°c Storage With High Precision

    High Precision and Specificity Mouse Resistin Retn ELISA Kit 96 Wells


    Cat.No E0263Mo

    *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 Nesfatin1 (also known as Retn) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.


    Reagent Provided

    ComponentsQuantity
    Standard Solution (96ng/ml)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 Retn 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

    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.


    Note

    • Sample concentrations should be predicted before being used in the assay. If the sample concentration is not within the range of the standard curve, users must contact us to determine the optimal sample for their particular experiments.
    • Samples to be used within 5 days should be stored at 2-8°C. Samples should be aliquoted or must be stored at -20°C within 1 month or -80°C within 6 months. Avoid repeated freeze thaw cycles.
    • Samples should be brought to room temperature before starting the assay.
    • Centrifuge to collect sample before use.
    • Samples containing NaN3 can’t be tested as it inhibits the activity of Horse Radish Peroxidase (HRP).
    • Collect the supernatants carefully. When sediments occurred during storage, centrifugation should be performed again.
    • Hemolysis can greatly impact the validity of test results. Take care to minimize hemolysis.

    *Sample can't be diluted with this kit. Owing to the the material we use to prepare the kit, the sample matrix interference may falsely depress the specificity and accuracy of the assay.


    Reagent Preparation

    All reagents should be brought to room temperature before use.

    Standard Reconstitute the 120μl of the standard (96ng/ml) with 120μl of standard diluent to generate a 48ng/ml standard stock solution. Allow the standard to sit for 15 mins with gentle agitation prior to making dilutions. Prepare duplicate standard points by serially diluting the standard stock solution (48ng/ml) 1:2 with standard diluent to produce 24ng/ml, 12ng/ml, 6ng/ml and 3ng/ml solutions. Standard diluent serves as the zero standard(0 ng/ml). Any remaining solution should be frozen at -20℃ and used within one month. Dilution of standard solutions suggested are as follows:


    48ng/mlStandard No.5120μl Original Standard + 120μl Standard Diluent
    24ng/mlStandard No.4120μl Standard No.5 + 120μl Standard Diluent
    12ng/mlStandard No.3120μl Standard No.4 + 120μl Standard Diluent
    6ng/mlStandard No.2120μl Standard No.3 + 120μl Standard Diluent
    3ng/mlStandard No.1120μl Standard No.2 + 120μl Standard Diluent

    Standard ConcentrationStandard No.5Standard No.4Standard No.3Standard No.2Standard No.1
    96ng/ml48ng/ml24ng/ml12ng/ml6ng/ml3ng/ml

    Wash Buffer Dilute 20ml of Wash Buffer Concentrate 30x into deionized or distilled water to yield 500 ml of 1x Wash Buffer. If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved.


    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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