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Bst 2.0 DNA Polymerase (Glycerolum liberum, alta densitas) HC5007A Image Featured
  • Bst 2.0 DNA Polymerase (Glycerolum liberum, alta densitas) HC5007A

Bst 2.0 DNA Polymerase (Glycerolum liberum, alta densitas)


Cat No: HC5007A

Sarcina: 1600U/8000U/80000U (32U/μL)

Bst DNA polymerase V2 ab Bacillo stearothermophilo DNA Polymerase I, quod habet.5′ → 3′DNA polymerase actio et fortis catena postea actio, sed no5′ → 3′actio exonuclease.

depictio producti

Product detail

Bst DNA polymerasis V2 derivatur ab Bacillo stearothermophilo DNA Polymerase I, quod actio polymerasis 5′ →3′ et catena valida postea activitatem exonucleasem habet, sed non est 5′ →3′ exonucleasis actio.Bst DNA Polymerase V2 optime convenit ad locum subductionis, amplificationis isothermal LAMPIS (Loop amplificationis isothermal mediatae) et celeris sequelae.Haec Bst DNA polymerasis V2 potest inhibere DNA polymerasi activitatem in cella temperie, ita ut exerceri possit et ratio reactionis formari potest ad temperaturas locus, impediendo non specificas amplificationes et amplificationem efficientiam reactionis, et haec versio potest. lyophilized potest.Praeterea capax est suam actionem in calidis temperaturis exsolvere, ita necessitatem separati activitatis gradus eliminare.


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  • Components

    Component

    HC5007A-01

    HC5007A-02

    HC5007A-03

    Bst DNA polymerase V2 (Glycerolum-free) (32U/μL)

    0.05 mL

    0.25 mL

    2.5 mL

    10×HC Bst V2 Buffer

    1.5 mL

    2×1.5 mL

    3×10 mL

    MgSO4 (100mM)

    1.5 mL

    2×1.5 mL

    2×10 mL

     

    Applications

    1.LUMEN isothermal amplificatio

    2.DNA litus unum obsessio reactionem

    3.Princeps GC gene sequencing

    4.DNA sequencia nanogram massa.

     

    Repono Condition

    Transportatio sub 0°C et reponenda -25°C~-15°C.

     

    Unitas Definition

    Una unitas definitur quantum enzyme, quod 25 nmol de dNTP in acidum insolubilem materiae 30 minutarum 65°C incorporet.

     

    LUMEN reactionem

    Components

    25 μLSystema

    10×HC Bst V2 Buffer

    2.5 μL

    MgSO4 (100mM)

    1.5 μL

    dNTPs (10mM quisque)

    3.5 μL

    SYTO™ 16 Green (25×)a

    1.0 μL

    Primario mixb

    6 μL

    Bst DNA Polymerase V2 (Glycerolum-free) (32 U/uL)

    0.25 μL

    Formula

    μL

    ddH₂O

    Usque ad 25 μL

    Notae:

    1) a.SYTOTM 16 Sedum (25×): Iuxta necessitates experimentales aliae colores in substitutis adhiberi possunt;

    2) b.Prima mix: permixtione 20 µM FIP, 20 µM BIP, 2.5 µM F3, 2.5 µM B3, 5 µM LF, 5 µM LB et alia uolumina.

     

    Reactio et Condition

    1 HC Bst V2 Buffer, temperatura incubationis est inter 60°C et 65°C.

     

    Calor Inactivation

    80°C, 20 min.

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