- Teks
- Sejarah
Due to the factthat the available t
Due to the fact
that the available traditional and immunological methods
for detecting toxigenic moulds are labor intensive and
time-consuming (Del Fiore et al. 2010), polymerase chain
reaction (PCR)-based methods could be good alternative to
traditional methods due to specificity, sensitivity and rapid-ness. Individual PCR protocols have been developed for the
detection of patulin producers (Puel et al.2010) as well as
ochratoxigenic (Bogs et al.2006) and aflatoxigenic
(Manonmani et al.2005) moulds. These PCR methods used
primer pairs designed from the isoepoxydon dehydrogenase
(idh), the non-ribosomal peptide syntethase (otanpsPN) and
the sterigmatocystin-O-methyltransferase (omt-1) genes
involved in the patulin, OTA and aflatoxin biosynthetic path-ways, respectively. Furthermore, several PCR methods based
on the above-mentioned genes have been recently reported to
detect patulin-, OTA- and aflatoxin-producingmoulds regard-less of genus and species (Luque et al.2011, 2012a, 2013)
that the available traditional and immunological methods
for detecting toxigenic moulds are labor intensive and
time-consuming (Del Fiore et al. 2010), polymerase chain
reaction (PCR)-based methods could be good alternative to
traditional methods due to specificity, sensitivity and rapid-ness. Individual PCR protocols have been developed for the
detection of patulin producers (Puel et al.2010) as well as
ochratoxigenic (Bogs et al.2006) and aflatoxigenic
(Manonmani et al.2005) moulds. These PCR methods used
primer pairs designed from the isoepoxydon dehydrogenase
(idh), the non-ribosomal peptide syntethase (otanpsPN) and
the sterigmatocystin-O-methyltransferase (omt-1) genes
involved in the patulin, OTA and aflatoxin biosynthetic path-ways, respectively. Furthermore, several PCR methods based
on the above-mentioned genes have been recently reported to
detect patulin-, OTA- and aflatoxin-producingmoulds regard-less of genus and species (Luque et al.2011, 2012a, 2013)
0/5000
Karena fakta
yang tersedia metode tradisional dan Imunologi
untuk mendeteksi toxigenic cetakan adalah tenaga kerja intensif dan
memakan waktu (Del Fiore et al. 2010), polimerase jaringan
reaksi (PCR)-berdasarkan metode bisa menjadi alternatif yang baik untuk
metode tradisional karena kekhususan, kepekaan dan cepat-ness. Individu PCR protokol telah dikembangkan untuk
Deteksi patulin produsen (Puel et al.2010) serta
ochratoxigenic (rawa et al.2006) dan aflatoxigenic
(Manonmani et al.2005) cetakan. Metode PCR ini digunakan
primer pasang dirancang dari dehydrogenase
(idh) isoepoxydon, peptida bebas-ribosomal syntethase (otanpsPN) dan
gen sterigmatocystin-O-methyltransferase (omt-1)
terlibat dalam patulin, OTA dan aflatoksin biosynthetic path-cara, masing-masing. Selain itu, beberapa metode PCR berbasis
pada gen disebutkan di atas telah baru-baru ini dilaporkan
mendeteksi patulin, OTA, dan aflatoksin-producingmoulds hal-kurang dari genus dan spesies (Luque et al.2011, 2012a, 2013)
yang tersedia metode tradisional dan Imunologi
untuk mendeteksi toxigenic cetakan adalah tenaga kerja intensif dan
memakan waktu (Del Fiore et al. 2010), polimerase jaringan
reaksi (PCR)-berdasarkan metode bisa menjadi alternatif yang baik untuk
metode tradisional karena kekhususan, kepekaan dan cepat-ness. Individu PCR protokol telah dikembangkan untuk
Deteksi patulin produsen (Puel et al.2010) serta
ochratoxigenic (rawa et al.2006) dan aflatoxigenic
(Manonmani et al.2005) cetakan. Metode PCR ini digunakan
primer pasang dirancang dari dehydrogenase
(idh) isoepoxydon, peptida bebas-ribosomal syntethase (otanpsPN) dan
gen sterigmatocystin-O-methyltransferase (omt-1)
terlibat dalam patulin, OTA dan aflatoksin biosynthetic path-cara, masing-masing. Selain itu, beberapa metode PCR berbasis
pada gen disebutkan di atas telah baru-baru ini dilaporkan
mendeteksi patulin, OTA, dan aflatoksin-producingmoulds hal-kurang dari genus dan spesies (Luque et al.2011, 2012a, 2013)
Sedang diterjemahkan, harap tunggu..
Due to the fact
that the available traditional and immunological methods
for detecting toxigenic moulds are labor intensive and
time-consuming (Del Fiore et al. 2010), polymerase chain
reaction (PCR)-based methods could be good alternative to
traditional methods due to specificity, sensitivity and rapid-ness. Individual PCR protocols have been developed for the
detection of patulin producers (Puel et al.2010) as well as
ochratoxigenic (Bogs et al.2006) and aflatoxigenic
(Manonmani et al.2005) moulds. These PCR methods used
primer pairs designed from the isoepoxydon dehydrogenase
(idh), the non-ribosomal peptide syntethase (otanpsPN) and
the sterigmatocystin-O-methyltransferase (omt-1) genes
involved in the patulin, OTA and aflatoxin biosynthetic path-ways, respectively. Furthermore, several PCR methods based
on the above-mentioned genes have been recently reported to
detect patulin-, OTA- and aflatoxin-producingmoulds regard-less of genus and species (Luque et al.2011, 2012a, 2013)
that the available traditional and immunological methods
for detecting toxigenic moulds are labor intensive and
time-consuming (Del Fiore et al. 2010), polymerase chain
reaction (PCR)-based methods could be good alternative to
traditional methods due to specificity, sensitivity and rapid-ness. Individual PCR protocols have been developed for the
detection of patulin producers (Puel et al.2010) as well as
ochratoxigenic (Bogs et al.2006) and aflatoxigenic
(Manonmani et al.2005) moulds. These PCR methods used
primer pairs designed from the isoepoxydon dehydrogenase
(idh), the non-ribosomal peptide syntethase (otanpsPN) and
the sterigmatocystin-O-methyltransferase (omt-1) genes
involved in the patulin, OTA and aflatoxin biosynthetic path-ways, respectively. Furthermore, several PCR methods based
on the above-mentioned genes have been recently reported to
detect patulin-, OTA- and aflatoxin-producingmoulds regard-less of genus and species (Luque et al.2011, 2012a, 2013)
Sedang diterjemahkan, harap tunggu..
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- Selamat malam dan selamat tidurSemoga mi
- Keselamatan
- Until I bad..I still love you..This is m
- Luar biasa
- Aku selalu rindu kamu
- Selamat
- Semoga mimpi indah
- Now I'm visiting makkah city
- Bad
- Riyadh city
- Aku selalu rindu kamu
- In this Tender we compete with Clamp On,
- Have a nice dreams
- Sad me
- Aku orang indonesia
- Aku Pengen ketemu kamu
- Aku sangat menyukai mu
- Alone
- maaf saya hanya bercanda, bukan serius
- There's always the way
- Aku akan menvintai kamu selamanya
- Don't be mad
- Kamu sangat cantik
- Satu
