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Mouse Transforming Growth Factor Beta 1 Elisa Test Kit for Research Use

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Mouse Transforming Growth Factor Beta 1 Elisa Test Kit for Research Use

China Mouse Transforming Growth Factor Beta 1 Elisa Test Kit for Research Use supplier

Large Image :  Mouse Transforming Growth Factor Beta 1 Elisa Test Kit for Research Use

Product Details:

Place of Origin: Shanghai, China
Brand Name: BT Lab
Certification: CE, ISO9001:2005, MSDS
Model Number: Cat.No E0660Mo

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
Payment Terms: Western Union, T/T
Supply Ability: In Stock
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Detailed Product Description
Target Protein: Transforming Growth Factor β1 Assay Time: 2 Hours
Sample: Serum,plasma,urine,tissue,cell Culture Supernatant Test Method: Sandwich
Custom: Available Delivery: Within 48 Hours

High specificity and precision Mouse Transforming Growth Factor Beta 1 ELISA kit 96 wells

 

Cat.No E0660Mo

Standard Curve Range: 5pg/ml - 2000pg/ml

Sensitivity: 2.48pg/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 Mouse Transforming Growth Factor Beta 1 (also known as TGF-B1) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.

 

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%

 

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.

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 (2400pg/ml ) with 120μl of standard diluent to generate a 1200pg/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 (1200pg/ml) 1:2 with standard diluent to produce 600pg/ml, 300pg/ml, 150pg/ml and 75pg/ml solutions. Standard diluent serves as the zero standard(0 pg/ml ). Any remaining solution should be frozen at -20°C and used within one month. Dilution of standard solutions suggested are as follows:

 

1200pg/ml Standard No.5 120μl Original Standard + 120μl Standard Diluent
600pg/ml Standard No.4 120μl Standard No.5 + 120μl Standard Diluent
300pg/ml Standard No.3 120μl Standard No.4 + 120μl Standard Diluent
150pg/ml Standard No.2 120μl Standard No.3 + 120μl Standard Diluent
75pg/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
2400pg/ml 1200pg/ml 600pg/ml 300pg/ml 150pg/ml 75pg/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.

 

References

Foitzik K., Lindner G., Mueller-Roever S., Maurer M., Botchkareva N., Botchkarev V., Handjiski B., Metz M., Hibino T., Soma T., Dotto G.P., Paus R.
FASEB J. 14:752-760(2000)

 

 

 

 

Contact Details
Shanghai Korain Biotech Co., Ltd

Contact Person: Lee

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