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Human F9 ELISA Kit
  MSPP-SEA840HU
 :  
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Human F9 ELISA Kit
  MSPP-SEA840HU
 :  SEA840HU
 :  

 

  • Assay duration:
    Multiple steps
  • Assay Type (ELISA with LOV):
    Sandwich
  • Conjugate ELISA:
    Biotin
  • Format:
    Pre-coated
  • Host:
    Rabbit
  • Primary antibody reactivity:
    Human
  • Target protein:
    F9
  • Size:
    1 kit
  • Sample Type:
    Plasma
  • Cross Reactivity:
    No significant cross-reactivity or interference between Coagulation Factor IX (F9) and analogues was observed
  • Detection Method:
    Colorimetric
  • Time to Results:
    3 h
  • Shelf Life:
    12 Months
  • Detection Range:
    78 - 5000 pg/ml
  • Storage Temperature:
    4 °C for one month (frequent use), −20 °C for one year
  • Sample Volume:
    100 µl
  • Sensitivity:
    34 pg/ml
  • Regulatory Status:
    RUO
  • Cat. No.:
    MSPP-SEA840HU
  • No. of tests:
    96 wells

 

 

This assay has high sensitivity and excellent specificity for detecting Human F9 (Coagulation Factor IX). The assay range is from 78 to 5000 pg/ml (Sandwich kit) with a sensitivity of 34 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%

Factor IX  is one of the serine proteases (EC 3.4.21.22) of the coagulation system; it belongs to peptidase family S1. Deficiency of this protein causes hemophilia B. It was discovered after a young boy named Stephen Christmas was found to be lacking this exact factor, leading to hemophilia, in 1952. Factor IX is inactive unless activated by factor XIa (of the contact pathway) or factor VIIa (of the tissue factor pathway). When activated into factor IXa, in the presence of Ca₂+, membrane phospholipids, and a Factor VIII cofactor, it hydrolyses one arginine-isoleucine bond in factor X to form factor Xa.Deficiency of factor IX causes Christmas disease (hemophilia B). Over 100 mutations of factor IX have been described; some cause no symptoms, but many lead to a significant bleeding disorder.

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