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SDC1 Sandwich Immunoassay Porcine ELISA Kit 96 Wells Size With High Specificity

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SDC1 Sandwich Immunoassay Porcine ELISA Kit 96 Wells Size With High Specificity

China SDC1 Sandwich Immunoassay Porcine ELISA Kit 96 Wells Size With High Specificity supplier

Large Image :  SDC1 Sandwich Immunoassay Porcine ELISA Kit 96 Wells Size With High Specificity

Product Details:

Place of Origin: Shanghai, China
Brand Name: BT Lab
Certification: CE, ISO9001:2015, MSDS
Model Number: Cat.No E0604Po

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
Size: 96 Wells/48 Wells Sensitivity: 1.26ng/ml
Standard Curve Range: 2ng/ml - 600ng/ml Shipping: DHL/FedEX
Sample: Serum,plasma,urine,tissue,cell Culture Supernatant Discount: Available

Porcine SDC1 Sandwich Immunoassay Test Kit 96 Wells Size With High Sensitivity and Specificity
 
Cat.No E0604Po
Intended Use
This sandwich kit is for the accurate quantitative detection of Porcine Syndecan-1 (also known as SDC1) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.
 
Assay Principle
This ELISA Test Kit is an Enzyme-Linked Immunosorbent Assay (ELISA). The plate has been pre-coated with Porcine SDC1 antibody. SDC1 present in the sample is added and binds to antibodies coated on the wells. And then biotinylated Porcine SDC1 Antibody is added and binds to SDC1 in the sample. Then Streptavidin-HRP is added and binds to the Biotinylated SDC1 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 Porcine SDC1. The reaction is terminated by addition of acidic stop solution and absorbance is measured at 450 nm.
*This product is for research use only, not for use in diagnosis procedures. It’s highly recommend to read this instruction entirely before use.
 
Precautions

  • Prior to use, the ELISA Test Kit and sample should be warmed naturally to room temperature 30 minutes.
  • This instruction must be strictly followed in the experiment.
  • Once the desired number of strips has been removed, immediately reseal the bag to protect the remain from deterioration. Cover all reagents when not in use.
  • Make sure pipetting order and rate of addition from well-to-well when pipetting reagents.
  • Pipette tips and plate sealer in hand should be clean and disposable to avoid cross-contamination.
  • Avoid using the reagents from different batches together.
  • Substrate solution B is sensitive to light, don’t expose substrate solution B to light for a long time.
  • Stop solution contains acid. Please wear eye, hand and skin protection when using this material. Avoid contact of skin or mucous membranes with kit reagent.
  • The kit should not be used beyond the expiration date.

 
Reagent Provided

ComponentsQuantity
Standard Solution (640ng/ml)0.5ml x1
Pre-coated ELISA Plate12 * 8 well strips x1
Standard Diluent3ml x1
Streptavidin-HRP6ml x1
Stop Solution6ml x1
Substrate Solution A6ml x1
Substrate Solution B6ml x1
Wash Buffer Concentrate (30x)20ml x1
Biotinylated Porcine ASDC1 Antibody1ml x1
User Instruction1
Plate Sealer2 pics
Zipper bag1 pic

 
Reagent Preparation
All reagents should be brought to room temperature before use.
Standard Reconstitute the 120μl of the standard (640ng/ml) with 120μl of standard diluent to generate a 320ng/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 (320ng/ml) 1:2 with standard diluent to produce 160ng/ml, 80ng/ml, 40ng/ml and 20ng/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:
 

320ng/mlStandard No.5120μl Original Standard + 120μl Standard Diluent
160ng/mlStandard No.4120μl Standard No.5 + 120μl Standard Diluent
80ng/mlStandard No.3120μl Standard No.4 + 120μl Standard Diluent
40ng/mlStandard No.2120μl Standard No.3 + 120μl Standard Diluent
20ng/mlStandard No.1120μl Standard No.2 + 120μl Standard Diluent

 

Standard ConcentrationStandard No.5Standard No.4Standard No.3Standard No.2Standard No.1
640ng/ml320ng/ml160ng/ml80ng/ml40ng/ml20ng/ml

 
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.
 
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.

Contact Details
Shanghai Korain Biotech Co., Ltd

Contact Person: Lee

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