Payment & Shipping Terms:
|Discount:||Available||Target Protein:||A1-Acid Glycoprotein|
|Storage:||2-8°C||Assay Length:||2 Hours|
|Bulk Order:||Yes||Sample:||Serum,plasma,urine,tissue,cell Culture Supernatant|
Porcine A1-Acid Glycoprotein Sandwich Test Kit High Specificity A1-AGP ELISA Assay kit
|Standard Solution (6400mg/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 Porcine A1-AGP Antibody||1ml x1|
|Plate Sealer||2 pics|
|Zipper bag||1 pic|
Standard Curve Range: 30mg/L - 6000mg/L
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.
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
This sandwich kit is for the accurate quantitative detection of Porcine A1-Acid Glycoprotein (also known as A1-AGP) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.
All reagents should be brought to room temperature before use.
Standard Reconstitute the 120μl of the standard (6400mg/L) with 120μl of standard diluent to generate a 3200mg/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 (3200mg/L) 1:2 with standard diluent to produce 1600mg/L, 800mg/L, 400mg/L and 200mg/L solutions. Standard diluent serves as the zero standard(0 mg/L). Any remaining solution should be frozen at -20°C and used within one month. Dilution of standard solutions suggested are as follows:
|3200mg/L||Standard No.5||120μl Original Standard + 120μl Standard Diluent|
|1600mg/L||Standard No.4||120μl Standard No.5 + 120μl Standard Diluent|
|800mg/L||Standard No.3||120μl Standard No.4 + 120μl Standard Diluent|
|400mg/L||Standard No.2||120μl Standard No.3 + 120μl Standard Diluent|
|200mg/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.
Contact Person: Lee