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High Precision Human ELISA Kit , 96 Wells Human Insulin ELISA Kit

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High Precision Human ELISA Kit , 96 Wells Human Insulin ELISA Kit

High Precision Human ELISA Kit , 96 Wells Human Insulin ELISA Kit
High Precision Human ELISA Kit , 96 Wells Human Insulin ELISA Kit

Large Image :  High Precision Human ELISA Kit , 96 Wells Human Insulin ELISA Kit

Product Details:

Place of Origin: Shanghai, China
Brand Name: BT Lab
Certification: CE, ISO9001:2005, MSDS
Model Number: Cat.No E0010Hu

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: T/T, Western Union
Supply Ability: In Stock
Detailed Product Description
Target Protein: Insulin Uniprot No.: P01308
Sensitivity: 0.11mIU/L Standard Curve Range: 0.2mIU/L - 60mIU/L
OEM: Acceptable Quality: CE, ISO
High Light:

elisa kit


enzyme immunoassay kit

96 wells Human specificity and precision INS ELISA Kit
Cat.No E0010Hu
Standard Curve Range: 0.2mIU/L - 60mIU/L
Sensitivity: 0.11mIU/L
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.
Intended Use
This sandwich kit is for the accurate quantitative detection of human Insulin (also known as INS) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.
Reagent Provided

Standard Solution (80mIU/L)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 human INS Antibody1ml x1
User Instruction1
Plate Sealer2 pics
Zipper bag1 pic


  • Prior to use, the 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 Preparation
Standard Reconstitute the 120μl of the standard (80mIU/L) with 120μl of standard diluent to generate a 40mIU/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 (40mIU/L) 1:2 with standard diluent to produce 20mIU/L, 10mIU/L, 5mIU/L and 2.5mIU/L solutions. Standard diluent serves as the zero standard(0 mIU/L). Any remaining solution should be frozen at -20°C and used within one month. Dilution of standard solutions suggested are as follows:

40mIU/LStandard No.5120μl Original Standard + 120μl Standard Diluent
20mIU/LStandard No.4120μl Standard No.5 + 120μl Standard Diluent
10mIU/LStandard No.3120μl Standard No.4 + 120μl Standard Diluent
5mIU/LStandard No.2120μl Standard No.3 + 120μl Standard Diluent
2.5mIU/LStandard No.1120μl Standard No.2 + 120μl Standard Diluent


Standard ConcentrationStandard No.5Standard No.4Standard No.3Standard No.2Standard No.1

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.

  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.

* This product is for research use only, not for use in diagnosis procedures. It’s highly recommend to read this instruction entirely before use.
Boesgaard T.W., Pruhova S., Andersson E.A., Cinek O., Obermannova B., Lauenborg J., Damm P., Bergholdt R., Pociot F., Pisinger C., Barbetti F., Lebl J., Pedersen O., Hansen T.
BMC Med. Genet. 11:42-42(2010)


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Contact Person: Lee

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