Kit ɗin RNAprep Pure Plant

Don tsarkake jimlar RNA daga tsirrai da fungi.

Kit ɗin RNAprep Pure Plant Kit yana ba da hanya mai sauri, mai sauƙi, kuma mai tsada don tsarkake jimlar RNA daga samfuran shuka ta amfani da ingantaccen shafi mai juyawa da tsarin buɗaɗɗen tsari na musamman. Kit ɗin ya ƙunshi RNase-Free Filtration Column CS don haɓakawa da tace tsire-tsire mai ɗumi ko lysates na fungal, da juzu'i na CR3 don tsarkake RNA mai inganci ta amfani da fasahar silica-membrane. Ana iya samun cikakken RNA mai inganci cikin mintuna 30-40. Dukan tsari mai sauƙi ne, mai sauƙi kuma mai lafiya don aiki tare da ƙarancin guba. RNA da aka samu yana da babban tsarki kuma baya da gurɓataccen furotin.

Cat. A'a	Girman shiryawa
4992237	50 prep

Aika mana imel

Bayanin samfur

Misalin Gwaji

Tambayoyi

Alamar samfur

Siffofin

Imi Ingantaccen buffers don samfuran shuka yana sa tsarin ya fi dacewa.
Que Unique DNase I yana rage gurɓacewar ƙwayoyin halittar DNA.
Column Shafin filtration na musamman CS yana kawar da wasu gurɓatattun abubuwa.
NA Babban tsabtataccen shirye-shiryen amfani RNA ya dace da aikace-aikacen da ke ƙarƙashin ƙasa masu mahimmanci.
■ Babu hakar phenol/chloroform, babu LiCl da hazo ethanol, kuma babu buƙatar csCl gradients centrifugation, wanda ke sa tsarin ya zama amintacce kuma abin dogaro.

Aikace -aikace

■ RT-PCR.
B Northern Blot, Dot Blot.
Haɗin PCR na ainihi.
Analysis Chip analysis.
Ing Binciken PolyA, fassarar in vitro, cloning kwayoyin.

Lura

Idan samfurin yana da wadata a cikin metabolism na biyu, ana iya amfani da Buffer HL da TIANGEN ya bayar don cimma matsakaicin ingancin tsarkakewa.

Duk samfuran ana iya keɓance su don ODM/OEM. Don cikakkun bayanai,don Allah danna Sabis na Musamman (ODM/OEM)

Na baya: TGuide S32 Magnetic Soil/Kit ɗin DNA

Na gaba:

	Abu: 80 MG Atenia cordifolia ganye Hanyar: An ware RNA na ganyayen Atenia cordifolia ta amfani da Kit ɗin RNAprep Pure Plant. Sakamako: Da fatan za a duba hoton agarose gel electrophoresis na sama. 2-4 μl na 100 elul eluates an ɗora su akan kowane layi. An yi electrophoresis a
	An kiyasta yawan amfanin RNA na samfura daban -daban

Tambaya: Toshewar shafi

A-1 Cell lysis ko homogenization bai isa ba

---- Rage amfani da samfur, ƙara yawan adadin lysis, ƙara homogenization da lokacin lysis.

A-2 Samfurin adadin ya yi yawa

---- Rage adadin samfurin da aka yi amfani da shi ko ƙara yawan adadin kuzarin lysis.

Tambaya: Ƙananan amfanin RNA

A-1 Rashin isasshen lysis na sel ko homogenization

---- Rage amfani da samfur, ƙara yawan adadin lysis, ƙara homogenization da lokacin lysis.

A-2 Samfurin adadin ya yi yawa

---- Don Allah koma zuwa matsakaicin ƙarfin sarrafawa.

A-3 RNA ba a fitar da shi gaba ɗaya daga shafi

---- Bayan ƙara ruwa RNase-Free, bar shi na 'yan mintoci kaɗan kafin a datse.

A-4 Ethanol a cikin mafi girma

---- Bayan rinsing, sake maimaita centrifuge kuma cire buhun wanki gwargwadon iko.

Ba a cire matsakaicin al'adar C-5 gaba ɗaya

---- Lokacin tattara sel, don Allah a tabbata an cire matsakaitan al'adu gwargwadon iko.

A-6 Kwayoyin da aka adana a cikin RNAstore ba su da tsattsauran ra'ayi

---- Yawan RNAstore ya fi matsakaicin matsakaicin al'adar salula; don haka yakamata a kara karfin centrifugal. An ba da shawarar yin centrifuge a 3000x g.

A-7 Ƙananan abun cikin RNA da yalwa a cikin samfurin

---- Yi amfani da samfuri mai kyau don sanin idan ƙarancin samfurin ya haifar da samfurin.

Tambaya: ƙasƙantar da RNA

A-1 Kayan ba sabo bane

---- Yakamata a adana sabbin kyallen takarda a cikin sinadarin nitrogen nan da nan ko kuma a saka su cikin reagent na RNAstore don tabbatar da tasirin hakar.

A-2 Samfurin adadin ya yi yawa

---- Rage adadin samfurin.

A-3 RNase gurbatawan

---- Ko da yake buffen da aka bayar a cikin kit ɗin bai ƙunshi RNase ba, yana da sauƙi a gurɓata RNase yayin aikin hakar kuma ya kamata a kula da shi sosai.

A-4 gurɓataccen Electrophoresis

---- Sauya mazubin electrophoresis kuma tabbatar da cewa abubuwan amfani da Load Buffer ba su da gurɓataccen RNase.

A-5 Ana yin lodin yawa don electrophoresis

---- Rage adadin lodin samfurin, lodin kowace rijiya kada ya wuce 2 μg.

Tambaya: Gurɓacewar DNA

A-1 Samfurin adadin ya yi yawa

---- Rage adadin samfurin.

A-2 Wasu samfurori suna da babban abun ciki na DNA kuma ana iya bi da su tare da DNase.

---- Yi maganin DNase na RNase-Free zuwa maganin RNA da aka samu, kuma ana iya amfani da RNA kai tsaye don gwaje-gwajen da suka biyo baya bayan magani, ko kuma za'a iya ƙara tsarkakewa ta kayan aikin tsarkakewa na RNA.

Tambaya: Yadda za a cire RNase daga kayan gwaji da gilashin gilashi?

Don gilashin gilashi, gasa a 150 ° C na tsawon awanni 4. Don kwantena na filastik, nutse cikin 0.5 M NaOH na mintuna 10, sannan a rinshe shi da ruwa mara RNase sannan a yi taɓo don cire RNase gaba ɗaya. Reagents ko mafita da aka yi amfani da su a cikin gwaji, musamman ruwa, dole ne su kasance marasa RNase. Yi amfani da ruwa mara RNase don duk shirye-shiryen reagent (ƙara ruwa zuwa kwalban gilashi mai tsabta, ƙara DEPC zuwa taro na ƙarshe na 0.1% (V/V), girgiza dare da autoclave).

Rubuta saƙonka a nan ka aika mana