Reagent Kit for Quantitative Determination of Creatine Kinase Activity in Human Serum or Plasma by UV Kinetic Method “CREATINE KINASE-UTS” according to TU 9398-028-59879815-2011

Reagent Kit for Quantitative Determination of Creatine Kinase Activity in Human Serum or Plasma by UV Kinetic Method “CREATINE KINASE-UTS” according to TU 9398-028-59879815-2011

Reagent kit: Creatine Kinase Activity Assay Kit

Intended use: This kit is intended for the determination of creatine kinase (CK) activity in human serum and plasma using a UV-kinetic method.

Technical specifications: TU 9398-028-59879815-2011

Kit composition:

• Reagent 1 – buffer-substrate solution:
  • Imidazole: 125 mmol/L
  • D-glucose: 25 mmol/L
  • N-acetyl-L-cysteine: 25 mmol/L
  • Magnesium acetate: 12.5 mmol/L
  • NADP: 2.5 mmol/L
  • EDTA: 2 mmol/L
  • Hexokinase: 6800 U/L
  • pH: 6.5 ± 0.2
• Reagent 2 – enzyme-cofactor solution:
  • ADP: 15.2 mmol/L
  • AMP: 25 mmol/L
  • Diadenosine pentaphosphate: 108 mmol/L
  • Glucose-6-phosphate dehydrogenase: 8800 U/L
  • Creatine phosphate: 250 mmol/L
  • pH: 8.8 ± 0.2

Documentation: Instructions for use, certificate of analysis (passport).

If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Quantitative Determination of Creatine Kinase Activity in Human Serum or Plasma by UV Kinetic Method “CREATINE KINASE-UTS” according to TU 9398-028-59879815-2011, then our information portal MEDCOMMERCE can help you with this. To do this, simply fill out the feedback form by clicking on the link FEEDBACK FORM.

The products posted on our website are approved for use in Russia by the state regulator Roszdravnadzor (Federal Service for Surveillance in Healthcare). The information is for informational purposes only.