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Customized Sortilin Human Elisa Kit 96 Wells , Sort1 Sandwich Elisa Kit

Good quality Human ELISA Kit for sales
Good quality Human ELISA Kit for sales
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Customized Sortilin Human Elisa Kit 96 Wells , Sort1 Sandwich Elisa Kit

China Customized Sortilin Human Elisa Kit 96 Wells , Sort1 Sandwich Elisa Kit supplier

Large Image :  Customized Sortilin Human Elisa Kit 96 Wells , Sort1 Sandwich Elisa Kit

Product Details:

Place of Origin: Shanghai, China
Brand Name: BT Lab
Certification: CE, ISO9001:2005, MSDS
Model Number: Cat.No E3966Hu

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
Lead Time: Within 48 Hours Cat.No: E3966Hu
Known As: SORT1 Test Method: Sandwich
Discount: Available Target Protein: Sortilin
Brand: BT Lab

Customized Human Sortilin ELISA Kit 96 Wells High Specificity SORT1 Sandwich ELISA Kits
 
Cat.No E3966Hu
Standard Curve Range: 0.05ng/ml - 20ng/ml
Sensitivity: 0.024ng/ml
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.
*This product is for research use only, not for use in diagnosis procedures. It’s highly recommend to read this instruction entirely before use.
 
Precision
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
Intra-Assay: CV<8%
Inter-Assay: CV<10%
 
Intended Use
This sandwich kit is for the accurate quantitative detection of Human Sortilin (also known as SORT1) in serum, plasma, cell culture supernates, cell lysates, tissue homogenates.
 
Material Required But Not Supplied

  • 37°C±0.5°C incubator
  • Absorbent paper
  • Precision pipettes and disposable pipette tips
  • Clean tubes
  • Deionized or distilled water
  • Microplate reader with 450 ± 10nm wavelength filter

 
Precautions

  • 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.

 
Specimen Collection
Serum Allow serum to clot for 10-20 minutes at room temperature. Centrifuge at 2000-3000 RPM for 20 minutes.
 
Plasma Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 15 minutes at 2000-3000 RPM at 2 - 8°C within 30 minutes of collection.
 
Urine Collect by sterile tube. Centrifuge at 2000-3000 RPM for approximately 20 minutes. When collecting pleuroperitoneal fluid and cerebrospinal fluid, please follow the procedures above-mentioned.
 
Cell Culture Supernatant Collect by sterile tubes when examining secrete components. Centrifuge at 2000-3000 RPM for approximately 20 minutes. Collect the supernatants carefully. When examining the components within the cell, use PBS (pH 7.2-7.4) to dilute cell suspension to the cell concentration of approximately 1 million/ml. Damage cells through repeated freeze-thaw cycles to let out the inside components. Centrifuge at 2000-3000 RPM for approximately 20 minutes.
 
Tissue Rinse tissues in PBS (pH 7.4) to remove excess blood thoroughly and weigh before homogenization. Mince tissues and homogenize them in PBS (pH7.4) with a glass homogenizer on ice. Thaw at 2-8°C or freeze at -20°C. Centrifuge at 2000-3000 RPM for approximately 20 minutes.
 
Reagent Preparation
All reagents should be brought to room temperature before use.
Standard Reconstitute the 120μl of the standard (24ng/ml) with 120μl of standard diluent to generate a 12ng/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 (12ng/ml) 1:2 with standard diluent to produce 6ng/ml, 3ng/ml, 1.5ng/ml and 0.75ng/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:
 

12ng/ml Standard No.5 120μl Original Standard + 120μl Standard Diluent
6ng/ml Standard No.4 120μl Standard No.5 + 120μl Standard Diluent
3ng/ml Standard No.3 120μl Standard No.4 + 120μl Standard Diluent
1.5ng/ml Standard No.2 120μl Standard No.3 + 120μl Standard Diluent
0.75ng/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
24ng/ml 12ng/ml 6ng/ml 3ng/ml 1.5ng/ml 0.75ng/ml

 
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.
 
Referances
"The lysosomal trafficking of sphingolipid activator proteins (SAPs) is mediated by sortilin."
Lefrancois S., Zeng J., Hassan A.J., Canuel M., Morales C.R.
EMBO J. 22:6430-6437(2003)

 

Contact Details
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Contact Person: Lee

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