PVUI-RO
Roche
Pvu I
from Proteus vulgaris
About This Item
Produits recommandés
Source biologique
bacterial (Proteus vulgaris)
Niveau de qualité
Forme
solution
Activité spécifique
5000 units/mL
Conditionnement
pkg of 100 U (10650137001 [5 U/μl])
pkg of 500 U (10650129001 [5 U/μl])
Fabricant/nom de marque
Roche
Paramètres
37 °C optimum reaction temp.
Couleur
colorless
pH
7.5-7.6 (37 °C)
Solubilité
water: miscible
Adéquation
suitable for molecular biology
Application(s)
life science and biopharma
sample preparation
Activité étrangère
Non specific endunuclease <10%
Non specific endunuclease, none detected
Température de stockage
−20°C
Spécificité
Recognition sites: CG°AT*CG
CG°AT*CG
Restriction site: CG°AT↓*CG
CG°AT↓*CG
Heat inactivation: No inactivation of Pvu I after incubation at 65 °C for 15 minutes.
Qualité
1μg λDNA is incubated for 16hours in 50μl SuRE/Cut Buffer H with an excess of Pvu I. The number of enzyme units which do not change the enzyme-specific pattern is stated in the certificate of analysis.
Absence of exonuclease activity
Approximately 5μg [3H] labeled calf thymus DNA are incubated with 3μl Pvu I for 4hours at +37°C in a total volume of 100μl 50mM Tris-HCl, 10mM MgCl2, 1mM Dithioerythritol, pH approximately 7.5. Under these conditions, no release of radioactivity is detectable, as stated in the certificate of analysis.
Profil d'ADN
- λ: 3
- φX174: 0
- Ad2: 7
- M13mp7: 1
- pBR322: 1
- pBR328: 1
- pUC18: 2
- SV40: 0
Définition de l'unité
Stockage et stabilité
Remarque sur l'analyse
Pvu I generates ends that are compatible with fragments generated by Pac I.
Isoschizomers
Pvu I is an isoschizomer to BspC I and Xor II.
Methylation sensitivity
Pvu I cleavage is not inhibited by overlapping dam-methylation at the site indicated (°) on the recognition sequence, but Pvu I fragments of DNA isolated from dam+ strains are not as readily religated as those isolated from dam- strains. Pvu I is inhibited by 5-methylcytosine at the indicated site (°) and by 4-methylcytosine.
SuRE/Cut Buffer System
The buffer in bold is recommended for optimal activity
- A: 50-75%
- B: 75-100%
- H: 100%
- L: 25-50%
- M: 50-75%
Incubation temperature
+37°C
Unit definition
One Unit is the enzyme activity that completely cleaves 1μg λDNA in 1 hour at +37°C in a total volume of 25μl SuRE/Cut Buffer H.
Heat inactivation
Pvu I cannot be heat inactivated by incubating it for 15 minutes at +65°C.
PFGE tested
Pvu I has been tested in Pulsed-Field Gel Electrophoresis (on bacterial chromosomes). For cleavage of genomic DNA (E. coli C 600) embedded in agarose for PFGE analysis, we recommend 10U of enzyme/μg DNA and 4 hour incubation time.
Ligation and recutting assay
Pvu I fragments obtained by complete digestion of 1 μg pBR322 DNA are ligated with 1U T4 DNA Ligase in a volume of 10μl by incubation for 16hours at +4°C in 66mM Tris-HCl, 5mM MgCl2, 5mM Dithiothreitol, 1mM ATP, pH 7.5 (at +20°C) resulting in >80% recovery of 1μg pBR322 DNA fragments.
Subsequent re-cutting with Pvu I yields >95% of the typical pattern of pBR322 DNA × Pvu I fragments.
Relative activity in PCR mix (Taq DNA Polymerase buffer) is less than 5%. The PCR mix contained λDNA, 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.
Autres remarques
Composants de kit seuls
- Enzyme Solution
- SuRE/Cut Buffer H 10x concentrated
Code de la classe de stockage
12 - Non Combustible Liquids
Classe de danger pour l'eau (WGK)
WGK 1
Point d'éclair (°F)
does not flash
Point d'éclair (°C)
does not flash
Certificats d'analyse (COA)
Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".
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Articles
The term “Restriction enzyme” originated from the studies of Enterobacteria phage λ (lambda phage) in the laboratories of Werner Arber and Matthew Meselson.
Contenu apparenté
Restriction endonucleases in prokaryotes function primarily to protect against foreign genetic material, notably bacteriophage DNA.
Restriction endonucleases in prokaryotes function primarily to protect against foreign genetic material, notably bacteriophage DNA.
Restriction endonucleases in prokaryotes function primarily to protect against foreign genetic material, notably bacteriophage DNA.
Restriction endonucleases in prokaryotes function primarily to protect against foreign genetic material, notably bacteriophage DNA.
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