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Human CD59 ELISA Kit
Human CD59 ELISA Kit
  MSPP-SEB336HU
 :  
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Human CD59 ELISA Kit
  MSPP-SEB336HU
 :  SEB336HU
 :  

 

  • Assay duration:
    Multiple steps
  • Assay Type (ELISA with LOV):
    Sandwich
  • Conjugate ELISA:
    Biotin
  • Format:
    Pre-coated
  • Host:
    Rabbit
  • Primary antibody reactivity:
    Human
  • Target protein:
    CD59
  • Size:
    1 kit
  • Sample Type:
    Serum, plasma, cell lysates and other biological fluids
  • Cross Reactivity:
    No significant cross-reactivity or interference between Cluster of Differentiation 59 (CD59) and analogues was observed
  • Detection Method:
    Colorimetric
  • Time to Results:
    3 h
  • Shelf Life:
    12 Months
  • Detection Range:
    12.5 - 800 pg/ml
  • Storage Temperature:
    4 °C for one month (frequent use), −20 °C for one year
  • Sample Volume:
    100 µl
  • Sensitivity:
    5.4 pg/ml
  • Regulatory Status:
    RUO
  • Cat. No.:
    MSPP-SEB336HU
  • No. of tests:
    96 wells

 

 

This assay has high sensitivity and excellent specificity for detecting Human CD59 (Cluster of Differentiation 59). The assay range is from 12.5 to 800 pg/ml (Sandwich kit) with a sensitivity of 5.4 pg/ml. There is no detectable cross-reactivity with other relevant proteins. Activity loss rate and accelerated stability test ect have been conducted to guarantee the best performance of the products after long storage and delivery.

  • High sensitivity and specificity
  • Perfect reproducibility and consistency across batches
  • Quality control with three-level inspections
  • Wide range of targets/species available
  • Intra-assay: CV<10%; Inter-assay: CV<12%

Protectin, a cell surface glycoprotein that regulates complement-mediated cell lysis, and it is involved in lymphocyte signal transduction. This protein is a potent inhibitor of the complement membrane attack complex, whereby it binds complement C8 and/or C9 during the assembly of this complex, thereby inhibiting the incorporation of multiple copies of C9 into the complex, which is necessary for osmolytic pore formation. This protein also plays a role in signal transduction pathways in the activation of T cells. Mutations in this gene cause CD59 deficiency, a disease resulting in hemolytic anemia and thrombosis, and which causes cerebral infarction. Multiple alternatively spliced transcript variants, which encode the same protein, have been identified for this gene.

 : For research use only. Not for use in clinical diagnostic procedures. Please proper stored each component based on the instruction.