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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® HinP1I (Hin6I)

FastDigest® HinP1I (Hin6I)

Kód produktu: FD0484 Kód výrobce: FD0484 Kód dodavatele: {AC30B38D-FBB4-41B3-993D-240736E50366} Výrobce: Life Technologies Czech Republic s.r.o.
FastDigest® HinP1I (Hin6I)
2 474,45 Kč
2 045,00 Kč bez DPH
do týdne
200 rxns

5'...G↓C G C...3'
3'...C G C↑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

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 AccI (XmiI), FastDigest AciI (SsiI), FastDigest AclI (Psp1406I), FastDigest Bsp119I, FastDigest BsaHI (Hin1I), FastDigest ClaI (Bsu15I), FastDigest Hpall, FastDigest MspI, FastDigest TaqI, AccI, AciI, AclI, BsaHI, Bsu15I, BsaHI, ClaI, Hin1I, Hin6I, HinP1I, HpaII, MspI, NarI, Psp1406I, SsiI, TaqI, XmiI.
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 HinP1I (Hin6I) is formulated to digest up to:

  • 1 µg of lambda DNA in 5 minutes
  • 1 µg of plasmid DNA in 10 minutes
  • 0.2 µg of PCR product in 5 minutes
  • 1 µg of genomic DNA in 5 minutes or 5 µg of genomic DNA in 60 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 10 5 5 2 80°C, 10 min 16

Methylation Effects

    Dam: never overlaps - no effect.
    Dcm: never overlaps - no effect.
    CpG: completely overlaps - blocked.
    EcoKI: never overlaps - no effect.
    EcoBI: never overlaps - no effect.
Methylation type Sequence Cleavage effect
CpG GCGC Blocked

Number of recognition sites in DNA molecules

Lambda ΦX174 M13mp18/19 pBR322 puc18/19 pUC57
215 18 26 31 17 17
pTZ19R/U pTZ57R pBluescriptIIKS(±) pBluescriptIISK(±) pACYC177 pACYC184
20 20 24 24 16 26

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
G^CGC
  • Hin1I (BsaHI)/FastDigest BsaHI (Hin1I)* (GR^CGCC)
  • NarI (GG^CGCC)
  • SsiI (AciI)/FastDigest AciI (SsiI)* (C^CGC)
  • HhaI/FastDigest HhaI
  • Hin6I (HinP1I)/FastDigest HinP1I (Hin6I)

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
G^CGC GCGCGC
  • Bsh1236I (BstUI)/FastDigest Bsh1236I
  • Cac8I
  • [HhaI/FastDigest HhaI]
  • [Hin6I (HinP1I)/FastDigest HinP1I (Hin6I)]
  • PauI (BssHII)/FastDigest BssHII (PteI)

Obsah balení

200 rxns

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