The RealStar® Malaria PCR Kit 1.0 is an in vitro diagnostic test, based on realtime PCR technology, for the detection of Plasmodium spp. specific DNA, including the five human pathogenic species Plasmodiumfalciparum, Plasmodiumvivax, Plasmodiummalariae, Plasmodiumovale and Plasmodiumknowlesi.
The RealStar® Malaria Screen & Type PCR Kit 1.0 is an in vitro diagnostic test, based on realtime PCR technology, for the detection and differentiation of DNA of the Plasmodium species Plasmodium malariae, Plasmodium ovale, Plasmodium knowlesi, Plasmodium vivax and Plasmodium falciparum. For read the product specific Key Features of this kit please klick Go-to
RealStar® Malaria PCR Kit 1.0 CE
RealStar® Malaria PCR Kit 1.0 CE
The RealStar® Malaria PCR Kit 1.0 CE consists of: Two Master reagents (Master A and Master B), Internal Control (IC), Positive Control, PCR grade water.
Products not licensed with Health Canada and not FDA cleared or approved. Kits not available in all countries.
Key Features
Detection of Plasmodium spp. specific DNA
Detection of all five currently known human pathogen Plasmodium species (P. falciparum, P. vivax, P. ovale, P. malariae and P. knowlesi )
Ready to use kit including Internal and Positive Control
Compatible with various real-time PCR platforms
CE-IVD marked in vitro Diagnostic Test
Plasmodium spp. specific DNA detected in the FAM detection channel [A]. Pink: P. falciparum; Blue: P. knowlesi; Turquoise: P. vivax; Orange: P. ovale; Green: P. malariae; Black: Negative Control; Red: Positive Control. The Internal Control (IC) is detected in the JOE detection channel [B]. channel [B].
RealStar Malaria PCR Kit 1.0 CE
Order No.
341013
Rxns
96
Transportation
Dry ice
For use with
Mx 3005PTM QPCR System
VERSANT® kPCR Molecular System AD
ABI Prism® 7500 SDS and 7500 Fast SDS
LightCycler® 480 Instrument II
Rotor-Gene® 6000
Rotor-Gene® Q 5/6 plex Platfom
CFX96™ Real-Time PCR Detection System
RealStar® Malaria Screen & Type PCR Kit 1.0 CE
RealStar® Malaria S&T PCR Kit 1.0 CE
The RealStar® Malaria S&T PCR Kit 1.0 CE consists of: Two Master reagents (Master A and Master B), Internal Control (IC), Positive Control Mix 1 [P. ovale, P. malariae, P. knowlesi], Positive Control Mix 2 [P. vivax, P. falciparum], PCR grade water.
Products not licensed with Health Canada and not FDA cleared or approved. Kits not available in all countries.
Key Features
Detection and differentiation of DNA of the Plasmodium species Plasmodium malariae, Plasmodium ovale, Plasmodium knowlesi, Plasmodium vivax . and Plasmodium falciparum.
Ready to use kit including Internal and Positive Control
Compatible with various real-time PCR platforms
CE-IVD marked in vitro Diagnostic Test
RealStar Malaria Screen & Type PCR Kit 1.0 CE
Order No.
351013
Rxns
2 x 48
Transportation
Dry ice
For use with
Mx 3005PTM QPCR System
VERSANT® kPCR Molecular System AD
ABI Prism® 7500 SDS and 7500 Fast SDS
LightCycler® 480 Instrument II
Rotor-Gene® 6000
Rotor-Gene® Q 5/6 plex Platfom
CFX96™ Real-Time PCR Detection System
CFX96™ Deep Well Real-Time PCR Detection System
RealStar® Malaria PCR Kit 1.0 CE
Instructions for use RealStar® Malaria PCR Kit 1.0 CE
Validation of a new real-time PCR based kit for detection and typing of 5 human pathogenic Plasmodium species, including P. knowlesi in whole blood specimen
Use of Capillary Blood Samples Leads to Higher Parasitemia Estimates and Higher Diagnostic Sensitivity of Microscopic and Molecular Diagnostics of Malaria Than Venous Blood Samples
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