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FastDigest® Restriction Enzymes
FastDigest® Enzymes
Digest DNA in 5-15 min,

#PF2010, 544 KB
FastDigest Restriction Enzymes
FastDigest Restriction Enzymes,
#P27, 1.34MB
FastDigest®  Green Buffer
FastDigest® Green Buffer,
715 KB
FastDigest®  Restriction Enzymes
FastDigest® Restriction Enzymes,
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FastDigest® enzymes are an advanced line of restriction enzymes for rapid DNA digestion. All FastDigest® enzymes are 100% active in the universal FastDigest® and FastDigest® Green buffers and are able to digest DNA in 5-15 minutes. More>>

Use these tools to plan your experiments:

  • REsearch™ – find restriction enzymes either by name or recognition sequence
  • REviewer™ – use for DNA sequence analysis, plasmid map creation and biochemical calculations
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Products » All » FastDigest® Restriction Enzymes » FastDigest® HpaII

FastDigest® Restriction Enzymes

FastDigest® HpaII

5'...C^C G  G...3'
3'...G  G C^C...5'
  • FastDigest® buffer for 100% activity - FastDigest® buffer for 100% activity
  • Optimal incubation at 37°C - Optimal incubation at 37°C
  • Ligation efficiency 95% - Ligation efficiency 95%
  • Cleavage blocked or impaired by CpG methylation - Cleavage blocked or impaired by CpG methylation
  • Thermal inactivation at 65°C in 5 min - Thermal inactivation at 65°C in 5 min
  • LO certified - LO certified
Catalog# Size, concentration Supplied with: Certificate of Analysis MSDS
10X FastDigest® Buffer 10X FastDigest® Green Buffer
FD0514 200 µl (200 react.) 1.00 ml 1.00 ml FD0514
Product information
Reaction conditions
Reaction temperature Digestion time with 1µl of FastDigest® enzyme, min bp from end of DNA required for complete digestion Thermal inactivation Incubation time without star activity, hours
Lambda, 1µg/20µl Plasmid DNA, 1µg/20µl PCR product, ~0.2µg/30µl Genomic DNA, 1µg/10µl
37°C 5 5 5 5 3 65°C, 5 min 16
Lambda DNA digested with FastDigest® HpaII

Lambda DNA
1.4% agarose
328 cleavage sites

Formulation
1 μl of enzyme (1 FDU) cleaves 1 μg of lambda DNA in 5 min at 37°C in 1X FastDigest® Buffer.

Recommended Reaction Conditions
1X FastDigest® buffer or 1X FastDigest® Green buffer at 37°C.
1 µl of FastDigest® HpaII is formulated to digest up to:
– 1 µg of lambda DNA in 5 min
– 1 µg of plasmid DNA in 5 min
– 0.2 µg of PCR product in 5 min
– 1 µg of genomic DNA in 5 min, or 5 µg of genomic DNA in 30 min.

Note

Isoschizomers
Search for commercial isoschizomers using REsearch™.

Compatible Ends
FastDigest® AccI (XmiI), FastDigest® AciI (SsiI), FastDigest® AclI (Psp1406I), FastDigest® BsaHI (Hin1I), FastDigest® Bsp119I, FastDigest® ClaI (Bsu15I), FastDigest® TaqI, AccI, AciI, AclI, BsaHI, Bsp119I, Bsu15I, ClaI, Hin1I, MaeII, NarI, Psp1406I, SsiI, TaqI, XmiI.

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

CCGG

Blocked
Number of recognition sites in DNA molecules
Lambda ΦX174 M13mp18/19 pBR322 puc18/19 pUC57
328 5 18 26 13 13
pTZ19R/U pTZ57R pBluescriptIIKS(-/+) pBluescriptIISK(-/+) pACYC177 pACYC184
12 12 13 13 16 34


Patents, Licenses, Trademarks
Protocols & recommendations
RECOMMENDATIONS FOR USE
ADDITIONAL PROTOCOLS

Fast Digestion of DNA

  1. Prepare the reaction mixture at room temperature in the order indicated:
    Component Volume
    Plasmid DNA Unpurified PCR product Genomic DNA
    Water, nuclease-free* 15 µl 17 µl 30 µl
    10X FastDigest® buffer or
    10X FastDigest® Green buffer
    2 µl 2 µl** 5 µl
    DNA* 2 µl (up to 1 µg) 10 µl (~0.2 µg) 10 µl (5 µg)
    FastDigest® enzyme 1 µl 1 µl 5 µl
    Total volume 20 µl 30 µl 50 µl
  2. Mix gently and spin down.
  3. Incubate at 37°C in a heat block or water thermostat for 5 min.***
  4. Inactivate the enzyme (optional).***
Note
* The volume of water should be corrected to keep the indicated total reaction volume. The volume of DNA can be scaled up to 10 µl or down to 0.5 µl depending on the DNA concentration.
** Only 2 µl of 10X FastDigest® buffer is required for unpurified PCR product in a 30 µl reaction volume.
*** See the Certificate of Analysis for enzyme and substrate specific incubation time and enzyme inactivation conditions.
Reaction Set-up for Digestion of Multiple DNA Samples

  1. Pipette 2 µl of each DNA sample* into labeled tubes.
  2. Prepare a master mix for n+1 samples.
    Example of master mix (for 10 samples of plasmid DNA):
    Water, nuclease-free (10 + 1) x 15 µl = 165 µl
    10X FastDigest® buffer or
    10X FastDigest® Green buffer
    (10 + 1) x 2 µl = 22 µl
    FastDigest® enzyme (10 + 1) x 1 µl = 11 µl
  3. Add 18 µl of master mix into tubes containing DNA
Note
* The volume of DNA can be scaled up to 10 µl or down to 0.5 µl depending on the DNA concentration. The volume of water and master mix should be corrected to keep the indicated total reaction volume.
Double and Multiple Digestion of DNA

FastDigest® enzymes allow simultaneous digestion of DNA with two or more enzymes in one digestion reaction.
  • Use 1 µl of each enzyme and scale up the reaction conditions appropriately.
  • The combined volume of all added enzymes should not exceed 1/10 of the total reaction volume.
  • If enzymes require different incubation temperature, perform sequential DNA cleavage: complete the first digestion reaction at the lower temperature, add the second enzyme and increase the digestion temperature for the second enzyme cleavage.
Scaling up DNA Digestion Reaction

DNA 1 µg 2 µg 3 µg 4 µg 5 µg
FastDigest® enzyme 1 µl 2 µl 3 µl 4 µl 5 µl
10X FastDigest® buffer or
10X FastDigest® Green buffer
2 µl 2 µl 3 µl 4 µl 5 µl
Total volume 20 µl 20 µl 30 µl 40 µl 50 µl
 
 
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