Payment & Shipping Terms:
|Assay Time:||2 Hours||Known As:||TBARS|
|Quality:||CE, ISO||Sample:||Serum,plasma,urine,tissue,cell Culture Supernatant|
Rat Strong Sensitivity Thiobarbituric Acid Reactive Substance Sandwich ELISA Kit With 2 Hours Assay Time
Standard Curve Range: 0.5nmol/ml - 100nmol/ml
Size: 96 wells
*This product is for research use only, not for use in diagnosis procedures. It’s highly recommend to read this instruction entirely before use.
|Standard Solution (128nmol/ml)||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 (25x)||20ml x1|
|Biotinylated Rat TBARS Antibody||1ml x1|
|Plate Sealer||2 pics|
|Zipper bag||1 pic|
This elisa kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Rat TBARS antibody. TBARS present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Rat TBARS Antibody is added and binds to TBARS in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated TBARS 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 Rat TBARS. 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 (128nmol/ml) with 120μl of standard diluent to generate a 64nmol/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 (64nmol/ml) 1:2 with standard diluent to produce 32nmol/ml, 16nmol/ml, 8nmol/ml and 4nmol/ml solutions. Standard diluent serves as the zero standard(0 nmol/ml). Any remaining solution should be frozen at -20°C and used within one month. Dilution of standard solutions suggested are as follows:
|64nmol/ml||Standard No.5||120μl Original Standard + 120μl Standard Diluent|
|32nmol/ml||Standard No.4||120μl Standard No.5 + 120μl Standard Diluent|
|16nmol/ml||Standard No.3||120μl Standard No.4 + 120μl Standard Diluent|
|8nmol/ml||Standard No.2||120μl Standard No.3 + 120μl Standard Diluent|
|4nmol/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|
Wash Buffer Dilute 20ml of Wash Buffer Concentrate 25x 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.
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.
Contact Person: Lee