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Potvrzuji
  1. Úvodní strana
  2. Reagencie
  3. Life Technologies / Fermentas
  4. FastDigest & CONVENTIONAL RESTRICTION ENZYMES
  5. FastDigest restrikční enzymy
  6. FastDigest® Sau3AI (Bsp143I)

FastDigest® Sau3AI (Bsp143I)

Kód produktu: FD0784 Kód výrobce: FD0784 Kód dodavatele: {AC215DEC-A51A-4F08-90CD-F74E58D9208E} Výrobce: Life Technologies Czech Republic s.r.o.
FastDigest® Sau3AI (Bsp143I)
2 510,75 Kč
2 075,00 Kč bez DPH
do týdne
40 rxns

5'...↓G A T C ...3'
3'... C T A G↑...5 

Zobraz detailní popis

Detailní popis

Thermo Scientific FastDigest enzymes are an advanced line of fast restriction enzymes that are all 100% active in the universal FastDigest and FastDigest Green reaction buffers.

The universal buffer allows rapid single-, double- or multiple DNA digestion within 5-15 minutes eliminating any need for buffer change or subsequent DNA clean-up steps. DNA modifying enzymes, such as Klenow Fragment, T4 DNA Ligase, alkaline phosphatases and T4 DNA Polymerase all have 100% activity in FastDigest Buffer. Therefore, enzymes for downstream applications can be directly added to the FastDigest reaction mix.

For additional convenience FastDigest Green Buffer includes a density reagent and two tracking dyes for direct loading of digestion reaction products on gels.

Short incubation times and optimal composition of the universal FastDigest Buffer eliminate star activity effects.

Features

  • 100% activity of all FastDigest enzymes in the universal buffer
  • 100% buffer compatibility with downstream applications
  • Complete digestion in 5-15 minutes
  • Direct loading on gels
  • No star activity
  • 176 FastDigest enzymes available

Applications

  • Molecular cloning
  • Restriction site mapping
  • Genotyping
  • Southern Blot
  • Restriction fragment length polymorphism (RFLP)
  • SNP analysis

Note

FastDigest® Sau3AI (Bsp143I), FastDigest® DpnI and FastDigest® MboI all recognize the same sequence but have different methylation sensitivities and cleavage positions.

The FastDigest Green Buffer offers the same high performance in DNA digestion and downstream applications as the colorless FastDigest Buffer. For applications that require product analysis by fluorescence excitation (e.g. concentration measurements in UV light) the colorless FastDigest Buffer is recommended.

For methylation sensitivity refer to product specifications.

Isoschizomers Search for commercial isoschizomers using REsearch.
Compatible Ends FastDigest BamHI, FastDigest BclI, FastDigest BglII, FastDigest PsuI, FastDigest Sau3AI (Bsp143I), BclI, BamHI, BglII, Bsp143I, PsuI.
Formulation 1 µL of enzyme (1 FDU) cleaves 1 μg of lambda DNA in 5 minutes at 37°C in 1X FastDigest Buffer.
Hazardous No
Recommended Reaction Conditions

1X FastDigest buffer or 1X FastDigest Green buffer at 37°C.
1 µL of FastDigest Sau3AI (Bsp143I) is formulated to digest up to:

  • 1 µg of lambda DNA in 5 minutes
  • 1 µg of plasmid DNA in 5 minutes
  • 0.2 µg of PCR product in 10 minutes
  • 1 µg of genomic DNA in 5 minutes or 5 µg of genomic DNA in 30 minutes
Storage Condition -20 C

Reaction conditions

Reaction temperature Digestion time with 1 µL of FastDigest enzyme, min bp from end of DNA required for complete digestion Thermal inactivation Incubation time without star activity, hours
Lambda, 1 µg/20 µL Plasmid DNA, 1 µg/20 µL PCR product, ~0.2 µg/30 µL Genomic DNA, 1 µg/10 µL
37°C 5 5 10 5 4 65°C, 20 min 16

Methylation Effects

    Dam: completely overlaps - no effect.
    Dcm: never overlaps - no effect.
    CpG: may overlap - blocked.
    EcoKI: never overlaps - no effect.
    EcoBI: may overlap - no effect.
Methylation type Sequence Cleavage effect
Dam(GATC) Gm6ATC No effect
CpG 5'...GATm5C G...3'
3'...CTA Gm5C...5'		 Blocked
EcoBI(TGA(N)8TGCT) 5'...TGm6ATC(N)6 TGCT...3'
3'...AC TAG(N)6m6ACGA...5'		 No effect

Number of recognition sites in DNA molecules

Lambda ΦX174 M13mp18/19 pBR322 puc18/19 pUC57
116 0 7 22 15 15
pTZ19R/U pTZ57R pBluescriptIIKS(±) pBluescriptIISK(±) pACYC177 pACYC184
15 15 15 15 22 15

New sites generated by ligation

Newly generated recognition sites resulting from ligation of protruding compatible DNA ends

Recognition Sequence Second Enzyme Enzymes recognizing newly generated recognition sequence
^GATC
  • BamHI/FastDigest BamHI (G^GATCC)
  • BclI/FastDigest BclI (T^GATCA)
  • BglII/FastDigest BglII (A^GATCT)
  • MboI/FastDigest MboI (^GATC)
  • PsuI (BstYI)/FastDigest PsuI* (R^GATCC)
  • PsuI (BstYI)/FastDigest PsuI* (R^GATCT)
  • Bsp143I (Sau3AI)/FastDigest Sau3AI (Bsp143I)
  • DpnI/FastDigest DpnI
  • MboI/FastDigest MboI

Newly generated recognition sites resulting from fill-in of 5'-overhang and self-ligation

Recognition Sequence Newly generated sequence after reaction Enzymes that cleave the newly generated sequence
^GATC GATCGATC
  • [Bsp143I (Sau3AI)/FastDigest Sau3AI (Bsp143I)]
  • Bsu15I (ClaI)/FastDigest ClaI (Bsu15I)
  • [DpnI/FastDigest DpnI]
  • [MboI/FastDigest MboI]
  • TaqI/FastDigest TaqI

Obsah balení

40 rxns

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