Kit ɗin Kwayoyin Tumatir Mai Saurin RNA Mai Sauki

Don tsabtace jimlar RNA mai inganci daga kyallen takarda.

Kit ɗin RNA Easy Fast Plant Tissue Kit shine kayan hakar RNA mai sauri don kyallen kyallen da aka haɓaka dangane da fasahar cire kwayoyin halittar DNA wanda TIANGEN ya haɓaka. Ba a buƙatar reagents masu guba kamar β-mercaptoethanol ko DTT yayin aikin, kuma ana iya kammala dukkan aikin hakar RNA a cikin mintuna 30. Ba wai kawai ya dace da samfuran ganye na tsire-tsire na yau da kullun kamar alkama da masara ba, har ma don samfuran polysaccharide/polyphenol masu ƙarfi kamar ganye na Malus spectabilis, ganye na auduga, ganyen chrysanthemum, furen hibiscus, tubar dankalin turawa, kankana, kokwamba, allurar pine , da dai sauransu.

Cat. A'a Girman shiryawa
4992880 50 prep

Bayanin samfur

Misalin Gwaji

Tambayoyi

Alamar samfur

Siffofin

■ Mai sauƙi da sauri: Jimlar hakar RNA daga samfuran shuka za a iya kammala shi cikin mintuna 30.
■ Karfin dacewa: Wannan kit ɗin ba kawai ya dace da samfuran tushe da ganye ba, har ma don samfuran polysaccharide/polyphenol.
Amintacce da ƙarancin guba: Ba a buƙatar reagents masu guba kamar β-mercaptoethanol, DTT, chloroform, phenol.

Aikace -aikace

Itable Ya dace da aikin da ke ƙasa, gami da RT-PCR, RT-qPCR, haɗaɗɗiyar guntu, Blot na Arewa, Dot Blot, gwajin PolyA, fassarar in vitro, nazarin kariyar RNase da ƙyallen ƙwayoyin cuta, da 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 Example Jimlar RNA na samfuran ganye na MG 65 (ganyen albasa, ganyen hibiscus, ganyen alkama, ganyen shinkafa, ganyen fruit ugli, Prunus cerasifera ganye, ganyen ɓaure, ganyen daylily, ganyen Kerria japonica), samfuran naman gwari 150 MG (Lentinus edodes) da 200 An samo samfuran petal na mg (furannin lily na rana) ta amfani da RNA Easy Fast Plant Tissue Kit. Sakamakon bincike na Bioanalyzer 2100 na jimlar RNA daga ganyen lily-lily.
    Experimental Example Agilent Bioanalyzer 2100 sakamakon bincike na jimlar RNA daga furen-lily.
     Experimental Example An samo RNA daga samfura daban -daban da aka jera a teburin ta amfani da Kit ɗin Raba Sauƙaƙe na RNA.
    Ƙarar murya: 50 μl; Ƙarar girma: 2 μl.
    An gudanar da electrophoresis a 6 V/cm na mintina 15 akan agarose 1%.
    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