Clostridium difficile toxin A/B gene(C.diff)

Description:

Hoc ornamentum in vitro qualitative detectioni clostridii difficile toxin A gene et toxin B gene in speciminibus ab aegris suspectum clostridium difficile contagium.


Product Detail

Product Tags

Product nomen

HWTS-OT031A Nuclei Acidum Detection Ornamentum Clostridium difficile toxin A/B gene (C.diff) (Fluorescens PCR)

Testimonium

CE

Epidemiologia

Clostridium difficile (CD), gram-positivum anaerobicum sporogenicum Clostridium difficile, est unum e praecipuis pathogenis causantibus infectiones nosocomiales intestinales.Amet, circiter 15%~25% diarrhoeae antimicrobialis relatae, 50%~75% colitis antimicrobialis actis et 95%~100% enteritis pseudomembranacei causatur per infectio difficilem Clostridium (CDI).Clostridium difficile est pathogen conditionale, inter modos toxigenicos et modos non toxigenicos.

Channel

FAM tcdAgene
ROX tcdBgene
VIC/HEX Internum Imperium

Technical Parameters

Repono

≤-18℃

Fasciae vita XII mensibus
Specimen Type scabellum
Tt ≤38
CV ≤5.0%
LoD 200CFU/mL
Specification hoc ornamento utuntur ad deprehendendas alios pathogenis intestinales sicut Escherichia coli, Staphylococcus aureus, Shigella, Salmonella, Vibrio parahaemolyticus, Group B Streptococcus, Clostridium difficile non-pathogenicum modos, Adenovirus, rotavirus, norovirus, influenza A virus, influenza B virus et genomic humanum. DNA, eventus omnes negativi sunt.
Applicabilis Instrumenta Acta Biosystems (VII)D Real-time PCR Systems

Acta Biosystems (VII)D Fast Verus-Tempus PCR Systems

QuantStudio®5 Real-time PCR Systems

SLAN-96P Real-time PCR Systems (Hongshi Medical Technology Co., Ltd.)

LightCycler®480 Real-time PCR system

LineGene (IX)DC Plus Verus-Tempus PCR Detection System(FQD-96A.HangzhouBioer technologia)

MA-6000 Real-time Quantitatis Thermal Cycler (Suzhou Molarray Co., Ltd.)

BioRad CFX96 Real-time PCR System

BioRad CFX Opus 96 Real-time PCR System

Opus O

Optio 1 .

Adde 180μL lysozyme quiddam ad praecipitatum (lysozymum ad 20mg/mL diluendum cum lysozymo diluente), pipettam bene miscere, et processum ad 37°C plusquam 30 minuta. Accipe 1.5mL tubi centrifugii RNAse/DNase-liberi; et adde180μL imperium positivum et imperium negativum in ordine.Add10μL imperium internum ad specimen probandum, imperium positivum, et imperium negativum in ordine, ac utere Acidum nuclei extractionis seu Purificationis Reagenti (YDP302) a Tiangen Biotech (Beijing) Co., Ltd. pro subsequenti sample DNA extractione, et Quaeso stricte sequi instructiones ad usus proprios gradus.Usus DNase / RNAse liberum H2O pro elution, et volumen commendabile est 100μL.

Optio II.

Accipe 1.5mL tubus centrifugii RNAse/DNase-liberi, et adde 200μL imperium positivum et imperium negativum in ordine.Add10μL imperium internum ad specimen probandum, imperium positivum, et imperium negativum in ordine, ac Macro & Micro-test Viralis DNA/RNA Kit (HWTS-3004-32, HWTS-3004-48, HWTS-3004- 96) et Macronem & Micro-test Automaticum Acidum Nucleicum Extractum (HWTS-3006).Extractio stricte exercenda est secundum instructionem ad usum, et volumen commendatur elutionis 80μL.

 


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