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Candida auris

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Exceptional value for money
Rapid detection of all clinically relevant subtypes
Positive copy number standard curve for quantification
Highly specific detection profile
High priming efficiency
Broad dynamic detection range (>6 logs)
Sensitive to < 100 copies of target Accurate controls to confirm findings

Detail

Description

Nucleic acid testing (NAT) is the method of choice for detection and quantification of a wide range of micro organisms. Primerdesign manufactures and supplies high quality quantitative real-time PCR kits for the detection and simultaneous quantification of numerous significant pathogens . A copy number standard curve is provided for quantification and an the internal extraction template (DNA or RNA), controls for the quality of the nucleic acid extraction and eliminates false negative results.

The kit is designed with the broadest possible detection profile to ensure that all clinically relevant strains and subtypes are detected*. Target sequences are selected by working with data from key opinion leaders in the field. Multiple sequence alignments and unprecedented real-time PCR expertise in design and validation ensure the best possible kit.

Details of the target and priming specificity are included in the individual handbooks above.

Packaged, optimised and ready to use. Expect Better Data.

Other Products

N-(Aminooxy-PEG2)-N-bis(PEG3-propargyl)

N-(Aminooxy-PEG2)-N-bis(PEG3-propargyl) consists of two terminal propargyl groups and an aminooxy group. The propargyl groups reacts with azide-bearing compounds or biomolecules via copper catalyzed Click Chemistry. The aminooxy group is reactive towards aldehydes to form oxime bonds. If a reductant is used, it will form a hydroxylamine linkage. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries. Aminooxy compounds are very reactive and sensitive; they cannot be stored for long term. Immediate use (within 1 week) is highly recommended.

HIT Control

Name of Product

HIT Control

Catalog Number

MQCOHIT 1

Short Info

The HIT Control (positive and negative) can be used for internal quality Control of the corresponding Milenia QuickLine HIT-Test (MQHIT 1/Z)

This product is only available in Germany!

Method/Platform

HIT-Lateral flow assay

Range/Assay Sensivity

positive and negative control

Test Principle

IgG antibodies are resposible for the heparin induced thrombocytopenia.

Immobilized anti-human IgG on the membrane of the test unit binds patients/control IgG-antibodies which are previously captured by the PF4/polyanion-complex which is detected by intensely colored gold nanoparticles.

The presence of PF4/polyanion-complex becomes visible at a colored test line. The surplus of gold particles continues to migrate through the membrane and is captured at the control line by specific antibodies.

IVD4144 HiPure FFPE RNA Kit

Introduction

HiPure FFPE RNA Kit supplies a simple and rapid RNA extraction for Formalin-fixed, paraffin-embedded (FFPE) tissue and sections samples. This kit is based on silica gel column purification technology, no phenol-chloroform extraction or alcohol precipitation. The whole extraction only takes 30 minutes (not including digestion time). RNA can be directly used for downstream applications such as RT-PCR, Northern blot, vitro translation and other experiments.

Details

Specifications

FeaturesSpecifications
Main FunctionsIsolation total RNA from FFPE tissue
ApplicationsRT-PCR, cDNA synthesis, second generation sequencing
ProductsRNA, miRNA
Purification methodMini spin column
Purification technologySilica technology, DNase
Process methodManual (centrifugation or vacuum)
Sample typeFFPE slice, FFPE embedded tissue
Sample amountTissue: <6 mgFFPE: <6 slices
Yield1-20μg
Elution volume≥15μl
Time per run≤30 minutes (after digestion)
Liquid carrying volume per column800μl


Principle

This product is based on silica column purification. Remove paraffin by Buffer DPS. Sample lysis withproteinase K digestion requires only 15 minutes. After lysis, samples are incubated at 80ºC for 15 minutes. Transfer to an adsorption column and RNA is adsorbed on the membrane, while protein is not adsorbed and is removed with filtration. After washing proteins and other impurities, RNA wasfinally eluted with low-salt buffer.

Advantages

  • Efficient removal of DNA – unique genomic DNA removal column without DNase treatment
  • High quality – high purity total RNA can be directly used in various sensitive downstream applications
  • Fast – several samples can be extracted in 60 minutes by column method
  • Safe – no phenol chloroform extraction required
  • Sensitive – RNA can be recovered at the level of PG

Kit Contents

ContentsIVD4144
Purification Times50 Preps
HiPure RNA Micro Columns50
2ml Collection Tubes50
Proteinase K24 mg
Protease Dissolve Buffer1.8 ml
DNase I600 μl
DNase Booster Buffer1.5 ml
Buffer DPS60 ml
Buffer FRL15 ml
Buffer RLC15 ml
Buffer RWC*10 ml
Buffer RW2*20 ml
RNase Free Water10 ml

Storage and Stability

Proteinase K should be stored at 2–8°C upon arrival. DNase I should be stored at -20°C. However, short-term storage (DNase I up to 1 weeks, Proteinase K up to 8 weeks) at room temperature(15–25°C) does not affect their performance. The remaining kit components can be stored at roomtemperature (15–25°C) and are stable for at least 18 months under these conditions.

Experiment Data