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Sandwich Type Bovine ELISA Kits 96 Wells Plate With Strong Sensitivity

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Sandwich Type Bovine ELISA Kits 96 Wells Plate With Strong Sensitivity

Sandwich Type Bovine ELISA Kits 96 Wells Plate With Strong Sensitivity
Sandwich Type Bovine ELISA Kits 96 Wells Plate With Strong Sensitivity

Large Image :  Sandwich Type Bovine ELISA Kits 96 Wells Plate With Strong Sensitivity

Product Details:

Place of Origin: Shanghai, China
Brand Name: BT Lab
Certification: CE, ISO9001:2015, MSDS
Model Number: Cat.No E0216Bo

Payment & Shipping Terms:

Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Wrapped with ice pack and styrofoam package
Delivery Time: 1-3 business days, bulk order within one week
Supply Ability: Western Union, T/T
Detailed Product Description
Cat.No: E0216Bo Sample: Serum,plasma,urine,tissue,cell Culture Supernatant
Assay Principle: Bovine Delivery: Within 48 Hours
Bulk Order: Yes Lead Time: Within 48 Hours
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sandwich elisa kit

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elisa assay kit

Sandwich Type 96 Wells Bovine Thyroxine ELISA Kit With Strong Sensitivity and Specificity
 

Cat.No E0216Bo

Standard Curve Range: 5ng/ml - 600ng/ml

Sensitivity: 2.61ng/ml

Size: 96 wells

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.

 

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%

 

Intended Use

This sandwich kit is for the accurate quantitative detection of Bovine Thyroxine (also known as T4) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.

 

Reagent Preparation

All reagents should be brought to room temperature before use.

Standard Reconstitute the 120μl of the standard (640ng/ml) with 120μl of standard diluent to generate a 320ng/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 (320ng/ml) 1:2 with standard diluent to produce 160ng/ml, 80ng/ml, 40ng/ml and 20ng/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:

 

320ng/ml Standard No.5 120μl Original Standard + 120μl Standard Diluent
160ng/ml Standard No.4 120μl Standard No.5 + 120μl Standard Diluent
80ng/ml Standard No.3 120μl Standard No.4 + 120μl Standard Diluent
40ng/ml Standard No.2 120μl Standard No.3 + 120μl Standard Diluent
20ng/ml Standard No.1 120μl Standard No.2 + 120μl Standard Diluent

 

Standard Concentration Standard No.5 Standard No.4 Standard No.3 Standard No.2 Standard No.1
640ng/ml 320ng/ml 160ng/ml 80ng/ml 40ng/ml 20ng/ml

 

Wash Buffer Dilute 20ml of Wash Buffer Concentrate 30x into deionized or distilled water to yield 600 ml of 1x Wash Buffer. If crystals have formed in the concentrate, mix gently until the crystals have completely dissolved.

 

Assay Procedure

1. Prepare all reagents, standard solutions and samples as instructed. Bring all reagents to room temperature before use. The assay is performed at room temperature.

2. Determine the number of strips required for the assay. Insert the strips in the frames for use. The unused strips should be stored at 2-8°C.

3. Add 50μl standard to standard well. Note: Don’t add antibody to standard well because the standard solution contains biotinylated antibody.

4. Add 40μl sample to sample wells and then add 10μl anti-T4 antibody to sample wells, then add 50μl streptavidin-HRP to sample wells and standard wells (Not blank control well). Mix well. Cover the plate with a sealer. Incubate 60 minutes at 37°C.

5. Remove the sealer and wash the plate 5 times with wash buffer. Soak wells with at least 0.35 ml wash buffer for 30 seconds to 1 minute for each wash. For automated washing, aspirate all wells and wash 5 times with wash buffer, overfilling wells with wash buffer. Blot the plate onto paper towels or other absorbent material.

6. Add 50μl substrate solution A to each well and then add 50μl substrate solution B to each well. Incubate plate covered with a new sealer for 10 minutes at 37°C in the dark.

7. Add 50μl Stop Solution to each well, the blue color will change into yellow immediately.

8. Determine the optical density (OD value) of each well immediately using a microplate reader set to 450 nm within 10 minuets after adding the stop solution.

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Shanghai Korain Biotech Co., Ltd

Contact Person: Lee

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