Reagent Kit for Quantitative Enzyme Immunoassay Determination of 17-Hydroxyprogesterone in Human Serum and Plasma ("SteroidELISA-17-OH-Progesterone") According to TU 9398-204-98539446-2011

Reagent Kit for Quantitative Enzyme Immunoassay Determination of 17-Hydroxyprogesterone in Human Serum and Plasma ("SteroidELISA-17-OH-Progesterone") According to TU 9398-204-98539446-2011

This reagent kit is intended for the quantitative determination of 17-hydroxyprogesterone in human serum and plasma using the ELISA (enzyme-linked immunosorbent assay) method.

According to TU 9398-204-98539446-2011.

• Calibrator samples based on human serum – 6 vials (lyophilized or liquid, 0.5 ml each)
• Strip set in frame – 1 package
• 17-OH-progesterone-peroxidase conjugate – 1 vial (9 ml)
• Concentrated saline wash buffer – 1 vial (14 ml)
• TMB substrate solution – 1 vial (14 ml)
• Stop reagent – 1 vial (14 ml)
• Control serum based on human serum – 1 vial (lyophilized or liquid, 0.5 ml)

If your organization wants to sell medical equipment, medical products or medical consumables in Russia, for example, Reagent Kit for Quantitative Enzyme Immunoassay Determination of 17-Hydroxyprogesterone in Human Serum and Plasma ("SteroidELISA-17-OH-Progesterone") According to TU 9398-204-98539446-2011, 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.