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Strong Precision Rat ELISA Kit 96 Wells With MSDS / CE Certification E0711Ra

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Strong Precision Rat ELISA Kit 96 Wells With MSDS / CE Certification E0711Ra

China Strong Precision Rat ELISA Kit 96 Wells With MSDS / CE Certification E0711Ra supplier

Large Image :  Strong Precision Rat ELISA Kit 96 Wells With MSDS / CE Certification E0711Ra

Product Details:

Place of Origin: Shanghai, China
Brand Name: BT Lab
Certification: CE, ISO9001:2005, MSDS
Model Number: Cat.No E0711Ra

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
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Detailed Product Description
Custom: Available OEM: Acceptable
Target Protein: Insulin-like Growth Factor Binding Protein 1 Sample: Serum,plasma,urine,tissue,cell Culture Supernatant
Uniprot No.: P21743 Customized: Acceptable

96 Wells High Precision and Specificity Rat IGFBP-1 ELISA Test Kit With 2 Hours Assay Time

 

Cat.No E0711Ra

Standard Curve Range: 0.5ng/ml - 200ng/ml

Sensitivity: 0.27ng/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.

 

Intended Use

This sandwich kit is for the accurate quantitative detection of Rat Insulin-like Growth Factor Binding Protein 1 (also known as IGFBP-1) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.

 

Reagent Provided

Components Quantity
Standard Solution (240ng/ml) 0.5ml x1
Pre-coated ELISA Plate 12 * 8 well strips x1
Standard Diluent 3ml x1
Streptavidin-HRP 6ml x1
Stop Solution 6ml x1
Substrate Solution A 6ml x1
Substrate Solution B 6ml x1
Wash Buffer Concentrate (30x) 20ml x1
Biotinylated Rat IGFBP-1 Antibody 1ml x1
User Instruction 1
Plate Sealer 2 pics
Zipper bag 1 pic

 

Reagent Preparation

All reagents should be brought to room temperature before use.

Standard Reconstitute the 120μl of the standard (240ng/ml) with 120μl of standard diluent to generate a 120ng/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 (120ng/ml) 1:2 with standard diluent to produce 60ng/ml, 30ng/ml, 15ng/ml and 7.5ng/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:

120ng/ml Standard No.5 120μl Original Standard + 120μl Standard Diluent
60ng/ml Standard No.4 120μl Standard No.5 + 120μl Standard Diluent
30ng/ml Standard No.3 120μl Standard No.4 + 120μl Standard Diluent
15ng/ml Standard No.2 120μl Standard No.3 + 120μl Standard Diluent
7.5ng/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
240ng/ml 120ng/ml 60ng/ml 30ng/ml 15ng/ml 7.5ng/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.

 

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-IGFBP-1 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.

 

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.

 

Referances

"Insulin regulation of insulin-like growth factor-binding protein-1 gene expression is dependent on the mammalian target of rapamycin, but independent of ribosomal S6 kinase activity."
Patel S., Lochhead P.A., Rena G., Fumagalli S., Pende M., Kozma S.C., Thomas G., Sutherland C.
J. Biol. Chem. 277:9889-9895(2002)

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