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M-MLV Reverse Transcriptase HC2003B Featured Image
  • M-MLV Reverse Transcriptase HC2003B

M-MLV Reverse Transcriptase


Saukewa: HC2003B

Kunshin: 10KU/50KU

RevScript Reverse transcriptase ana samun su ta fasahar injiniyan kwayoyin halitta.

Bayanin Samfura

Bayanin samfur

RevScript Reverse transcriptase ana samun su ta fasahar injiniyan kwayoyin halitta.Yana da ƙarfin haɗin cDNA mafi girma, kwanciyar hankali na thermal da iyakar zafin jiki (har zuwa 60 ° C).Samfurin cDNA da aka haɗa ya kai 10kb.Yana haɓaka alaƙar samfuran kuma ya dace da jujjuya rubutun samfuran RNA tare da hadadden tsari na sakandare ko ƙananan kwafi.


  • Na baya:
  • Na gaba:

  • Abubuwan da aka gyara

    Bangaren

    HC2003B-01

    (10,000U)

    HC2003B-02

    (5*10,000U)

    HC2003B-03

    (200,000U)

    RevScript Reverse Transcriptase (200U/μL)

    50 μl

    5 × 50 ml

    1 ml

    5 × RevScript Buffer

    250 ml

    1.25 ml

    ml 5

     

    Yanayin Ajiya

    Ya kamata a adana wannan samfurin a -25 ° C ~ -15 ° C na shekaru 2.

     

    Ma'anar Naúrar

    Raka'a ɗaya ta haɗa 1 nmol na dTTP cikin kayan acid-insoluble a cikin mintuna 10 a 37°C ta amfani da Oligo(dT) a matsayin masu farawa.

     

    Saitin Amsa

    1.Denaturation na RNA samfuri (Wannan mataki na zaɓi ne, ƙirƙira samfurin RNA yana taimakawa buɗe tsarin na biyu, wanda zai haɓaka yawan amfanin ƙasan cDNA na farko.)

     

    Abubuwan da aka gyara

    girma (μL)

    RNase kyauta ddH2O

    Zuwa 13

    Oligo(dT)18 (50 μmol/L)

    ko Random Primer (50 μmol/L)

    Ko Takaddun Matsalolin Halitta (2 μmol/L)

    1

    ko 1

    ko 1

    Samfurin RNA

    Xa

     

    Bayanan kula: 

    1) a: Jimlar RNA: 1-5 ug ko mRNA: 1-500 ng

    2) Sanya a 65 ° C na minti 5, sa'an nan kuma canjawa kan kankara nan da nan don yin sanyi na minti 2.Taƙaitaccen centrifugation don tattara ruwa mai amsawa, ƙara bayanin amsawar juyi kamar yadda aka nuna a tebur mai zuwa.A hankali pipette don haɗuwa.

    1.Shirye-shiryen cakuda dauki (20 μL girma)

    Abubuwan da aka gyara

    girma (μL)

    Cakuda matakin da ya gabata

    13

    5× Buffer

    4

    dNTP Mix (10nmol/L)

    1

    Rubutun Juya (200 U/μL)

    1

    Mai hana RNase (40 U/μL)

    1

     1.Yi martani a ƙarƙashin sharuɗɗa masu zuwa:

    Zazzabi (°C)

    Lokaci

    25 °Ca

    5 min

    42 °Cb

    15-30 min

    85 °Cc

    5 min

    Bayanan kula:

    1) a.Ana buƙatar haɓakawa a 25°C na 5mins kawai don amfani da hexamers bazuwar.Da fatan za a tsallake wannan matakin lokacin amfani da Oligo (dT)18ko Gene Specific Primer.

    2) b.Matsakaicin zafin juzu'i da aka ba da shawarar shine 42°C, Don samfura masu sarƙaƙƙiya tsarin sakandare ko babban abun ciki na GC, ana ba da shawarar ɗaga yawan zafin jiki zuwa 50-55°C.

    3) c.Dumama a 85°C na tsawon mintuna 5 don hana juyar da rubutu.

    4) Ana iya amfani da samfurin kai tsaye a cikin halayen PCR ko qPCR, ko adana shi a -20°C don ajiyar ɗan gajeren lokaci.An ba da shawarar a daidaita samfuran kuma adana a -80 ° C don adana dogon lokaci.Guji daskarewa akai-akai.

    5) Samfurin ya dace da mataki ɗaya na RT-qPCR, ana bada shawara don ƙara 10-20 U reverse transcriptase ga kowane tsarin amsawa na 25μL, ko a hankali ƙara adadin juzu'in juzu'i bisa ga ainihin halin da ake ciki.

     

    Bayanan kula

    1.Da fatan za a tsabtace wurin gwaji;Ya kamata a sanya safofin hannu masu tsabta da abin rufe fuska yayin aiki.Duk abubuwan da ake amfani da su a cikin gwajin yakamata su kasance masu 'yanci na RNase don hana gurɓacewar RNase.

    2.Duk hanyoyin ya kamata a yi akan kankara don hana lalata RNA.

    3.High ingancin samfuran RNA ana bada shawarar don tabbatar da ingantaccen ingantaccen juzu'i.

    4.Wannan samfurin ne don amfani da bincike kawai.

    5. Da fatan za a yi aiki da riguna na lab da safofin hannu masu zubarwa, don amincin ku.

    Ku rubuta sakonku anan ku aiko mana