Reagent Kit for Determining Total α-Amylase Activity Using the Kinetic Method in Serum, Plasma, and Urine (α-AMYLASE DDS) According to TU 21.20.23.110-013-48813770-2016

The reagent kit for determining the total activity of α-amylase using the kinetic method in serum, plasma, and urine (α-AMYLASE DDS) is manufactured in compliance with TU 21.20.23.110-013-48813770-2016.

Execution Variant:

Variant 1 includes:

Reagent 1: buffer-enzyme solution, pH 7.15
Reagent 2: buffer-substrate solution, pH 7.15

Available Configurations:

Reagent 1: 2 vials (20 ml each); Reagent 2: 1 vial (10 ml)
Reagent 1: 5 vials (20 ml each); Reagent 2: 1 vial (25 ml)
Reagent 1: 2 vials (68 ml each); Reagent 2: 2 vials (17 ml each)
Reagent 1: 6 vials (68 ml each); Reagent 2: 6 vials (17 ml each)
Reagent 1: 2 vials (64 ml each); Reagent 2: 2 vials (20 ml each)
Reagent 1: 6 vials (64 ml each); Reagent 2: 6 vials (20 ml each)
Reagent 1: 2 vials (65 ml each); Reagent 2: 2 vials (20 ml each)
Reagent 1: 6 vials (65 ml each); Reagent 2: 6 vials (20 ml each)
Reagent 1: 4 vials (65 ml each); Reagent 2: 4 vials (20 ml each)
Reagent 1: 4 vials (38 ml each); Reagent 2: 2 vials (22 ml each)
Reagent 1: 6 vials (24 ml each); Reagent 2: 3 vials (13 ml each)
Reagent 1: 6 vials (16 ml each); Reagent 2: 6 vials (4.0 ml each)
Reagent 1: 5 vials (62 ml each); Reagent 2: 5 vials (18 ml each)
Reagent 1: 4 vials (20 ml each); Reagent 2: 4 vials (5.0 ml each)
Reagent 1: 1 vial (40 ml); Reagent 2: 1 vial (10 ml)
Reagent 1: 2 vials (40 ml each); Reagent 2: 1 vial (20 ml)
Reagent 1: 4 vials (20 ml each); Reagent 2: 1 vial (20 ml)
Reagent 1: 4 vials (60 ml each); Reagent 2: 1 vial (60 ml)

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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.

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