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Kidney Injury Molecule 1 Kim 1 Elisa Kit , High Precision Elisa 96 Well Plate

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    Buy cheap Kidney Injury Molecule 1 Kim 1 Elisa Kit , High Precision Elisa 96 Well Plate from wholesalers
     
    Buy cheap Kidney Injury Molecule 1 Kim 1 Elisa Kit , High Precision Elisa 96 Well Plate from wholesalers
    • Buy cheap Kidney Injury Molecule 1 Kim 1 Elisa Kit , High Precision Elisa 96 Well Plate from wholesalers
    • Buy cheap Kidney Injury Molecule 1 Kim 1 Elisa Kit , High Precision Elisa 96 Well Plate from wholesalers

    Kidney Injury Molecule 1 Kim 1 Elisa Kit , High Precision Elisa 96 Well Plate

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    Brand Name : BT Lab
    Model Number : Cat.No E1099Hu
    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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    Kidney Injury Molecule 1 Kim 1 Elisa Kit , High Precision Elisa 96 Well Plate

    96 Wells 48 Wells High Precision and Specificity Human Kim 1 ELISA Kit


    Cat.No E1099Hu

    Storage: Store the reagents at 2-8°C. For over 6-month storage refer to the expiration date keep it at -20°C. Avoid repeated thaw cycles. If individual reagents are opened it is recommended that the kit be used within 1 month.

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


    Assay Principle

    This kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with human Kim-1 antibody. Kim-1 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated human Kim-1 Antibody is added and binds to Kim-1 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated Kim-1 antibody. After incubation unbound Streptavidin-HRP is washed away during a washing step. Substrate solution is then added and color develops in proportion to the amount of human Kim-1. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.


    Reagent Provided

    ComponentsQuantity
    Standard Solution (12.8ng/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 human Kim-1 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

    Precision

    Intra-Assay Precision (Precision within an assay) Three samples of known concentration were tested on one plate to assess intra-assay precision.

    Inter-Assay Precision (Precision between assays) Three samples of known concentration were tested in separate assays to assess inter-assay precision.

    CV(%) = SD/mean x 100

    Intra-Assay: CV<8%

    Inter-Assay: CV<10%


    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.

    Reagent Preparation

    All reagents should be brought to room temperature before use.

    Standard Reconstitute the 120μl of the standard (12.8ng/ml) with 120μl of standard diluent to generate a 6.4ng/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 (6.4ng/ml) 1:2 with standard diluent to produce 3.2ng/ml, 1.6ng/ml, 0.8ng/ml and 0.4ng/ml solutions. Standard diluent serves as the zero standard(0 ng/ml). Any remaining solution should be frozen at -20°C and used within one month. Dilution of standard solutions suggested are as follows:


    6.4ng/mlStandard No.5120μl Original Standard + 120μl Standard Diluent
    3.2ng/mlStandard No.4120μl Standard No.5 + 120μl Standard Diluent
    1.6ng/mlStandard No.3120μl Standard No.4 + 120μl Standard Diluent
    0.8ng/mlStandard No.2120μl Standard No.3 + 120μl Standard Diluent
    0.4ng/mlStandard No.1120μl Standard No.2 + 120μl Standard Diluent

    Standard ConcentrationStandard No.5Standard No.4Standard No.3Standard No.2Standard No.1
    12.8ng/ml6.4ng/ml3.2ng/ml1.6ng/ml0.8ng/ml0.4ng/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.


    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.

    References

    "Genetic susceptibility to respiratory syncytial virus bronchiolitis in preterm children is associated with airway remodeling genes and innate immune genes."
    Siezen C.L., Bont L., Hodemaekers H.M., Ermers M.J., Doornbos G., Van't Slot R., Wijmenga C., Houwelingen H.C., Kimpen J.L., Kimman T.G., Hoebee B., Janssen R.
    Pediatr. Infect. Dis. J. 28:333-335(2009)

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