ELK Biotechnology

Human SOX10(Sex Determining Region Y Box Protein 10) ELISA Kit

Product Code:
 
ELK9120
Product Group:
 
ELISA Kits
Supplier:
 
ELK Biotechnology
Regulatory Status:
 
RUO
Target Species:
 
Human
Application:
 
Enzyme-Linked Immunosorbent Assay (ELISA)
 

No additional charges, what you see is what you pay! *

CodeSizePrice
ELK9120-48T48T£298.00
Quantity:
ELK9120-96T96T£390.00
Quantity:
Prices exclude any Taxes / VAT
How to order with us   Contact us
Stay in control of your spending. These prices have no additional charges, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: China.
Typical lead time: 14-21 working days.
Contact us for more accurate information.
  • Videos
  • Further Information
  • Show All

Video

Further Information

Alternative Names:
DOM; MGC15649; SOX 10; SRY (sex determining region Y) box 10; SRY box 10; SRY box containing gene 10; SRY related HMG box gene 10
Assay Length:
3.5h
Assay Type:
Sandwich
Detection Range:
0.16-10 ng/mL
Sample Type:
Tissue homogenates, cell lysates and other biological fluids
Sensitivity:
0.048 ng/mL
Standard:
10 ng/mL
Test Principle:
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Human SOX10. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human SOX10. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Human SOX10, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ? 10nm. The concentration of Human SOX10 in the samples is then determined by comparing the OD of the samples to the standard curve.