Direct Pcr
Quid Direct PCR
Directus PCR est modus amplificationis DNA directe exsanguis, animalis TEXTUS,rat caudam,cellula,rat aurem,zebra piscispisces ova;plant folia,seminibusvel alius textus originalis biologici exempli sine DNA segregationis et purificationis gradus faciendo.Per ars directa multum tempus experimentale minuere potest, et sumptus in genotyping et quantitate incepta.Meliorem etiam optionem praebet prae provocationibus augendi minimam quantitatis specimen ubi purificationis gradus potentialiter ad damnum specimen ducere potuit.
PRAECESSATIO PCR Mix validam vim resistendi habet, propter praevisum robur patentatum Taq enzyme (patentes auctoritate: ZL20161034512.0 (China), EP3450560 (Europe), PCT/CN2017/082154 (US), patent 6894926 (Iaponia)).Eius Taq enzyme DNA recombinatione technologia utitur ad recombinationem DNA ligandi structuram regionis archaealis nucleici acidi ligandi interdum cum calefactione repugnanti Taq DNA polymerasi ad construendum exemplum DNA cum affinitate aucta.Melioratus calidus-initium Taq quod varias functiones originalis DNA polymerase retinet. Haec Taq enzyme ligare potest ad DNA templates et inchoare DNA synthesin in low intentionum intentionum et complexorum ambitus.
For exempli gratia,ittam facile addendo tuumcella;plant (folium novellum, radix vel semen) vel animalis ad specimenquiddam, et addit unicumdominus miscerespecificaprimers in pcr tubes ac per scelerisque currendo currendo.Ornamentum efficientiae est specimen pro magna-scalarum analysi analysi ubi tempus salutaris maximi momenti est.
Systema reactionis PCR continentis UNG enzyme et dUTP eligitur secundum experimenta requisita, quae inquinationem per amplificationem PCR productorum effectorum efficaciter vitare possunt.
CommodaDirect PCR *
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| Direct Pcr | Traditional methodo (RNA purgatio+ Coventional PCR) |
| Materia consummatio | TEXTUS consummatio | Minus | Multum |
| Formula praeparationis | Materia genus | Nullus stridor requiratur | exempla molendum |
| Operatio | One-tube type，10min | multiplex operatio, 1h * | |
| Flux | 1-96 | 1-24 | |
| PCR reactionem | reactionem ratio | Optimized 2×PCR mix | Dntp, MgCl2,10×PCR Buffer, Taq enzyme, |
Aapplication
01 Lepidium sativum microorganismi pathogenicum
02 identificatio genetice mutatio, genotyping
03 Multiplex PCR / SNP detectio / PCR-RFLP
04Sequencing / exquisitis
Product Series
| Series | Product Name | Specifications | Catalogue Number | Repono Conditions |
| Plant Direct PCR Series | 200 ×20μl rxns | TP-02111 | Pars I 4℃，Pars II -20℃ | |
| 2000 ×20μl rxns | TP-02113 | |||
| 200 ×20μl rxns | TP-02121 | Pars I 4℃，Pars II -20℃ | ||
| 2000 ×20μl rxns | TP-02123 | |||
| Plant Folium Direct PCR Plus Kit | 200 ×20μl rxns | TP-02131 | Pars I 4℃，Pars II -20℃ | |
| 2000 ×20μl rxns | TP-02133 | |||
| Plant Folium Direct PCR Plus Ornamentum -UNG | 200 ×20μl rxns | TP-02141 | Pars I 4℃，Pars II -20℃ | |
| 2000 ×20μl rxns | TP-02143 | |||
| 200 ×20μl rxns | TP-03111 | Pars I 4℃，Pars II -20℃ | ||
| 2000 ×20μl rxns | TP-03113 | |||
| 200 ×20μl rxns | TP-03121 | Pars I 4℃，Pars II -20℃ | ||
| 2000 ×20μl rxns | TP-03123 | |||
| 200 ×20μl rxns | TP-03131 | Pars I 4℃，Pars II -20℃ | ||
| 2000 ×20μl rxns | TP-03133 | |||
| 200 ×20μl rxns | TP-03141 | Pars I 4℃，Pars II -20℃ | ||
| 2000 ×20μl rxns | TP-03143 | |||
| Plant Semen Direct PCR Plus Kit I (Polysaccharide polyphenolum planta) | 200 ×20μl rxns | TP-03151 | Pars I 4℃，Pars II -20℃ | |
| 2000 ×20μl rxns | TP-03153 | |||
| Plant Semen Direct PCR Plus Kit I - UNG (Polysaccharide polyphenolum planta) | 200 ×20μl rxns | TP-03161 | Pars I 4℃，Pars II -20℃ | |
| 2000 ×20μl rxns | TP-03163 | |||
| 200 ×20μl rxns | TP-03171 | Pars I 4℃，Pars II -20℃ | ||
| 2000 ×20μl rxns | TP-03173 | |||
| Plant Semen Direct PCR Plus Kit II - UNG (Polysaccharide polyphenolum planta) | 200 ×20μl rxns | TP-03181 | Pars I 4℃，Pars II -20℃ | |
| 2000 ×20μl rxns | TP-03183 |
