Payment & Shipping Terms:
|Assay Time:||2 Hours||Sample:||Serum,plasma,urine,tissue,cell Culture Supernatant|
|Size:||96 Wells/48 Wells||Test Method:||Sandwich|
sandwich elisa kit,
elisa test kit
High Precision and Sensitivity Bovine Non-esterified Fatty Acid ELISA Assay Kit For Research
|Standard Solution (640μmol/L)||0.5ml x1|
|Pre-coated ELISA Plate||12 * 8 well strips x1|
|Standard Diluent||3ml x1|
|Stop Solution||6ml x1|
|Substrate Solution A||6ml x1|
|Substrate Solution B||6ml x1|
|Wash Buffer Concentrate (30x)||20ml x1|
|Biotinylated Bovine NEFA Antibody||1ml x1|
|Plate Sealer||2 pics|
|Zipper bag||1 pic|
Material Required But Not Supplied
Standard Curve Range: 2μmol/L - 600μmol/L
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.
This sandwich kit is for the accurate quantitative detection of Bovine Non-esterified Fatty Acid (also known as NEFA) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.
This ELISA Assay Kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Bovine NEFA antibody. NEFA present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Bovine NEFA Antibody is added and binds to NEFA in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated NEFA 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 Bovine NEFA. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.
All reagents should be brought to room temperature before use.
Standard Reconstitute the 120μl of the standard (640μmol/L) with 120μl of standard diluent to generate a 320μmol/L 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 (320μmol/L) 1:2 with standard diluent to produce 160μmol/L, 80μmol/L, 40μmol/L and 20μmol/L solutions. Standard diluent serves as the zero standard(0 μmol/L). Any remaining solution should be frozen at -20°C and used within one month. Dilution of standard solutions suggested are as follows:
|320μmol/L||Standard No.5||120μl Original Standard + 120μl Standard Diluent|
|160μmol/L||Standard No.4||120μl Standard No.5 + 120μl Standard Diluent|
|80μmol/L||Standard No.3||120μl Standard No.4 + 120μl Standard Diluent|
|40μmol/L||Standard No.2||120μl Standard No.3 + 120μl Standard Diluent|
|20μmol/L||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|
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.
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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