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生物源
bacterial (Proteus vulgaris)
品質等級
形狀
solution
比活性
5000 units/mL
包裝
pkg of 100 U (10650137001 [5 U/μl])
pkg of 500 U (10650129001 [5 U/μl])
製造商/商標名
Roche
參數
37 °C optimum reaction temp.
顏色
colorless
pH值
7.5-7.6 (37 °C)
溶解度
water: miscible
適合性
suitable for molecular biology
應用
life science and biopharma
sample preparation
異物活動
Non specific endunuclease <10%
Non specific endunuclease, none detected
儲存溫度
−20°C
特異性
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.
品質
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.
DNA分析
- λ: 3
- φX174: 0
- Ad2: 7
- M13mp7: 1
- pBR322: 1
- pBR328: 1
- pUC18: 2
- SV40: 0
單位定義
儲存和穩定性
分析報告
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.
其他說明
仅试剂盒组分
- Enzyme Solution
- SuRE/Cut Buffer H 10x concentrated
儲存類別代碼
12 - Non Combustible Liquids
水污染物質分類(WGK)
WGK 1
閃點(°F)
does not flash
閃點(°C)
does not flash
商品
The term “Restriction enzyme” originated from the studies of Enterobacteria phage λ (lambda phage) in the laboratories of Werner Arber and Matthew Meselson.
The term “Restriction enzyme” originated from the studies of Enterobacteria phage λ (lambda phage) in the laboratories of Werner Arber and Matthew Meselson.
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