SPH I
SPH I Basic information
- Product Name:
- SPH I
- Synonyms:
-
- Einecs 286-569-8
- restriction endonuclease apa I from*acetobacter P
- Nuclease, restriction endodeoxyribo-, SphI
- RESTRICTION ENDONUCLEASE APA I FROM*ACET OBACTER PAS
- RESTRICTION ENDONUCLEASE SPH I FROM*STRE PTOMYCES
- apa i from acetobacter pasteurianus
- sph i from streptomyces phaeochromogenes
- RESTRICTION ENDONUCLEASE APA I
- CAS:
- 85270-15-1
- MW:
- 0
- EINECS:
- 286-569-8
- Product Categories:
-
- 3.1.x.x Acting on esters
- 3.x.x.x Hydrolases
- Molecular Biology
- Molecular Biology Enzymes
- Molecular Biology Tested
- Restriction EndonucleasesApplication Index
- Restriction EnzymesEnzyme Class Index
- Mol File:
- Mol File
SPH I Chemical Properties
- storage temp.
- −20°C
- form
- buffered aqueous glycerol solution
MSDS
- Language:English Provider:SigmaAldrich
SPH I Usage And Synthesis
General Description
Compatible ends
Apa I ends are not compatible with those generated by any other known restriction enzymes.
Isoschizomers
Apa I is an isoschizomer to Bsp 120 I and Psp OMI.
Methylation sensitivity
Apa I is inhibited by 5′-methylcytosine at the sites indicated (*) in the recognition sequence.
Activity in SuRE/Cut Buffer System
Buffer printed in bold face type is the buffer recommended for optimal activity:
ABLMH
100%10-25%50-75%50-75%0-10%
Relative activity in complete PCR mix
Relative activity in PCR mix (Taq DNA Polymerase buffer) is 100%. The PCR mix contained target DNA, primers, 10 mM Tris-HCl (pH 8.3, +20°C), 50 mM KCl, 1.5 mM MgCl2, 200 μM dNTPs, 2.5 U Taq DNA polymerase. The mix was subjected to 25 amplification cycles. Activity in reaction buffer of Pwo SuperYield DNA Polymerase PCR Mix is 10%. When supplemented with GC-RICH Solution activity is increased to >100%.
Incubation temperature
+30°C
Unit definition
One unit is the enzyme activity that completely cleaves 1 μg ? × Hind III fragments in 1 hour at +30°C in a total volume of 25 μl SuRE/Cut Buffer A.
Heat inactivation
The enzyme can be heat inactivated by incubating it for 15 minutes at +65°C.
Number of cleavage sites on different DNAs
λAd2SV40φ X174M13mp7M13mp18pBR322pBR328pUC18
112 1000000
Ligation and recutting assay
Apa I fragments obtained by complete digestion of 1 μg λ × Hind III fragments are ligated with 1 U T4 DNA Ligase in a volume of 10 μl by incubation for 16 hours at +4°C in 66 mM Tris-HCl, 5 mM MgCl2, 5 mM Dithiothreitol, 1 mM ATP, pH 7.5 (at +20°C) resulting in >95% recovery of 1 μg λ × Hind III fragments.
Subsequent re-cutting with Apa I yields >95% of the typical pattern of λ × Hind III× Apa I fragments.
SPH ISupplier
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- 821-50328103-801 18930552037
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- 021-61998208 18217752821
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