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Human anti-phospholipid antibody ELISA Kit

NR-R10129

$780.00

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Principle
Indirect ELSIA, Antigen coated plate
 
Detection Range
0 - 100 U/ml
 
Size
96T
 
Specificity                                     NA

Sensitivity                                     0.5 U/ml
 
Assay time
~ 60 min
 
Shelf Life
12 Months from the Manufacturing Date
 
Storage
Store at 2 - 8ºC. 
 
Sample volume
10 µL Serum or Plasma
 
Detection Method
Chromogenic
  
Kit Components
 
 
 
1. 20 x wash buffer: 1vial 
 
 
2. One 96-well plate precoated with recombinant antigen
 
 
3. Assa diluent buffer: 1 vial
 
 
4. HRP conjugated: 2 vials
 
 
5. Positive Control: 1 vial
 
 
6. Negative Control:1vial
 
 
7. Calibrator set: 6 vials
 
 
8. TMB substrate: 1 vial
 
 
9. TMB stop solution: 12 ml.

 

Background

 

Antiphospholipid syndrome or antiphospholipid antibody syndrome (APS or APLS), or often also Hughes syndrome, is an autoimmune, hypercoagulable state caused by antiphospholipid antibodies. Phospholipids in the blood are required for the blood to clot. Thus, APS provokes blood clots (thrombosis) in both arteries and veins as well as pregnancy-related complications. Antiphospholipid syndrome can be primary or secondary. Primary antiphospholipid syndrome occurs in the absence of any other related disease. Secondary antiphospholipid syndrome occurs with other autoimmune diseases, such as systemic lupus erythematosus (SLE). Antiphospholipid syndrome often requires treatment with anticoagulant medication such as heparin to reduce the risk of further episodes of thrombosis. 

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