Tumbin Magnetic/Cell/Jinin Kit ɗin RNA

Cire RNA daga samfura daban -daban kamar jinin sel ɗin nama tare da babban kayan aiki.

Tumbin Magnetic/Cell/Jumlar RNA Kit ɗin yana ɗaukar beads na magnetic tare da aikin rabuwa na musamman da tsarin keɓaɓɓen tsari don rarrabewa da tsarkake jimlar RNA mai inganci. Za'a iya daidaita samfurin daidai da Kingfisher Flex96 da TGuide S32/S96 Extractors Nucleic Acid Extractors. Idan ana buƙatar haɓakar kayan sarrafawa ta atomatik, tuntuɓi TIANGEN don maganin haɗin kai.

Cat. A'a Girman shiryawa
4992740 50 prep

Bayanin samfur

Misalan Gwaji

Tambayoyi

Alamar samfur

Siffofin

■ Mai sauƙi da sauri: Za a iya samun jimlar RNA a cikin mintuna 60.
■ Babban kayan aiki: Yana iya cika buƙatun hakar da hannu da kuma haɓakar batutuwa akan dandamali daban-daban.
■ Amintacce kuma mara guba: Ba a buƙatar reagent kamar phenol/chloroform.

Musammantawa

Nau'in: Haɗin nau'in beads na Magnetic.
Samfurin: Kwayoyi, sel da jini.
Manufa: Jimlar RNA
Fara farawa: 5-20 MG, kada ya wuce 1 × 107, 0.1-1.5 ml
Lokacin aiki: 60 min
Aikace-aikacen ƙasa: RT-PCR/RT-qPCR, ginin ɗakin karatu na NGS, da dai sauransu.

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


  • Na baya:
  • Na gaba:

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    Experimental Examples An fitar da jimlar RNA daga hanta berayen 20 MG tare da TIANGEN Magnetic Tissue/Cell/Blood Total RNA Kit da samfuran da suka dace daga wasu masu siyarwa. An ɗora 5 μl na 200 μl eluate zuwa 1% electrophoresis na agarose, 6 V/cm.
    Kammalawa: Yawan hakar, tsarkin da kwanciyar hankali na TIANGEN Magnetic Tissue/Cell/Blood Total RNA Kit sun fi na sauran masu ba da kaya.
    Experimental Examples An fitar da jimlar RNA daga 20 MG na koda bera tare da TIANGEN Magnetic Tissue/Cell/Blood Total RNA Kit a cikin TIANGEN TGuide S32 ko Thermo Kingfisher Flex96 bi da bi. An ɗora 5 μl na 200 μl eluate zuwa 1% electrophoresis na agarose, 6 V/cm. Alamar: TIANGEN D15000 Alamar DNA.
    Kammalawa: Kayan Magnetic Tissue/Cell/Blood Total RNA Kit yana da kyakkyawan haɓakar hakar da tsarkin a cikin masu cirewa 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