New England Biolabs, R3150S, PvuI-HF®

PvuI-HF has been reformulated with Recombinant Albumin (rAlbumin) beginning with Lot #10128368. Related Categories Restriction Endonucleases P R,, High-Fidelity (HF®) Restriction Endonucleases,, Time-Saver Qualified Restriction Enzymes Applications Fast Cloning: Accelerate your cloning workflows with reagents from NEB,, Restriction Enzyme Digestion Specification Unit Definition One unit is defined as the amount of enzyme required to digest 1 µg of pXba DNA in 1 hour at 37°C in a total reaction volume of 50 μl. Reaction Conditions 1X rCutSmart™ Buffer Incubate at 37°C 1X rCutSmart™ Buffer 50 mM Potassium Acetate 20 mM Tris-acetate 10 mM Magnesium Acetate 100 µg/ml Recombinant Albumin (pH 7.9 @ 25°C) Activity in NEBuffers NEBuffer™ r1.1: 25% NEBuffer™ r2.1: 100% NEBuffer™ r3.1: 100% rCutSmart™ Buffer: 100% Diluent Compatibility Diluent B Storage Buffer 10 mM Tris-HCl 300 mM NaCl 1 mM DTT 0.1 mM EDTA 500 µg/ml Recombinant Albumin 50% Glycerol pH 7.4 @ 25°C Heat Inactivation No Methylation Sensitivity dam methylation: Not Sensitive dcm methylation: Not Sensitive CpG Methylation: Blocked FAQ Q: How can I search for a restriction enzyme by sequence, overhang or name? A: Enzyme finder, a new tool available on our website in the sidebar under "Favorite Tools", can be used to search for restriction enzymes by name, sequence, overhang or type. NEB enzymes include enzyme properties icons and are displayed as links. Q: How should I stop my restriction digest? A: If no further manipulations of the digested DNA are planned, the reaction can be terminated by adding a stop solution. At NEB, we use the following stop solution: 50% glycerol, 50 mM EDTA (pH 8.0), and 0.05% bromophenol blue (10 μl / 50 μl reaction). If further manipulations of the digested DNA are required, heat inactivation (raising the temperature to 65 or 80°C for 20 minutes) is the simplest method of stopping a reaction. Since this method does not work for all restriction enzymes, refer to the catalog information for the particular enzyme(s) you are using. Phenol/chloroform extraction is another means of inactivating a restriction enzyme. Q: How stable is a particular restriction enzyme? A: All enzymes are assayed for activity every 3-6 months; the most recent assay date is given on the label attached to each vial of enzyme. After thirty years of experience with restriction enzymes, we have found that most are very stable when stored at -20°C in the recommended storage buffer. Exposure to temperatures above -20°C should be minimized whenever possible. Q: When should I choose the HF version of the enzyme? A: The HF version of the enzyme has the same cleavage specificity as the wild type enzyme, and should be chosen if star activity is a concern or if the recommended buffer is more convenient for double digestion or other multi-step protocol. There is no disadvantage to using the HF version. Q: When is star activity a concern? A: Star activity is of concern if extra banding can cause misinterpretation of results in genotyping and mutational analysis procedures. Experimental design can promote star activity. Small reaction volumes are more likely to contain glycerol concentrations of 5% or greater, a condition known to increase star activity. A 5% glycerol concentration occurs when setting up a double digest in a 20 µl reaction using 1 µl of each enzyme. Overnight digests are more likely to generate star activity. For tips on avoiding star activity, please click here. Q: How should I set up a restriction digest? A: Most researchers follow the general rule that 10 units of restriction endonuclease is sufficient to overcome variability in DNA source, quantity and purity. Generally, 1 μl of enzyme is added to 1 μg of purified DNA in a final volume of 50 μl of the appropriate 1X NEBuffer followed by incubation for 1 hour at the recommended temperature. If an excess of enzyme is used, the length of incubation can often be decreased to save time. Alternatively, you can productively digest with fewer units of enzyme for up to 16 hours with many restriction enzymes. To keep glycerol concentration at less than 5% in a reaction, the restriction enzyme, which is supplied in 50% glycerol, should not exceed 10% of the total reaction volume An extremely important, yet often overlooked, element of a successful restriction digest is mixing. The reaction must be thoroughly mixed to achieve complete digestion. We recommend gently pipetting ther reaction mixture up and down or "flicking" the reaction tube. Follow with a quick ("touch") spin-down in a microcentrifuge. Do not vortex the reaction. Q: I don't see any cleavage after my restriction digest. What factors can interfere with cleavage? A: The preparation of DNA to be cleaved should be free of contaminants such as phenol, chloroform, alcohol, EDTA, detergents, or excessive salts, all of which can interfere with restriction enzyme activity. DNA methylation is also an important element of a restriction digest. If you are having difficulty cleaving your DNA substrate, we recommend the following control reactions. Incubate experimental DNA without restriction enzyme (degradation of DNA indicates contamination in the DNA preparation or reaction buffer) and control DNA (DNA with multiple known sites for the enzyme, e.g. lambda or adenovirus-2 DNA) with restriction enzyme to more accurately judge whether or not the reaction went to completion. If the control DNA is cleaved and the experimental DNA resists cleavage, the two DNAs can be mixed to determine if an inhibitor is present in the experimental sample. If an inhibitor (often salt, EDTA or phenol) is present, the control DNA will not cut after mixing. Q: How can I generate a restriction enzyme site map for my sequence? A: NEBcutter®, a computer program for restriction enzyme site mapping is available on the NEB web site in the sidebar under "Favorite Tools". The program accepts sequences retrieved from a local file or GenBank. It also accepts an input sequence pasted into a designated field. When presented with a sequence, NEBcutter will find the largest open reading frames within the sequence and indicate those restriction enzymes that could be used to excise the gene. It also locates the positions of all restriction enzymes that cut only once within the sequence chosen. NEBcutter is also fully aware of the information on the methylation sensitivity of restriction enzymes and alerts a user to overlapping methylation by dam, dcm, etc. Q: What information is available in the Restriction Enzyme Database (REBASE)? A: The Restriction Enzyme Database (REBASE), found in the sidebar under ""Favorite Tools"" on our web site, is a comprehensive database of information about restriction enzymes and related proteins. It contains published and unpublished references, recogntion and cleavage sites, isoschizomers, commercial availability, methylation sensitivity, crystal and sequence data. DNA methyltransferases, homing endonucleases, nicking enzymes, specificity subunits and control proteins are also included. Most recently, putative DNA methyltransferases and restriction enzymes, as predicted from analysis of genomic sequences, have been added. Q: Is extended digestion (incubation times > 1 hour) recommended? A: The unit definition of our restriction enzymes is based on a 1 hour incubation. Incubation time may be shortened if additional units of restriction enzyme are added to the reaction. Conversely, longer incubation times are often used to allow a reaction to proceed to completion with fewer units of enzyme. This is contingent on how long a particular enzyme can survive (maintain activity) in a reaction. Some enzymes survive for long periods (> 16 hours) while others survive only an hour or less in a reaction. For each restriction enzyme, we report the minimum number of units (1.0, 0.5, 0.25 or 0.13) required to digest 1 µg of substrate DNA in 16 hours. Enzymes that require less than 1 unit can be used at lower concentrations for extended incubation times. Note that DNA substrates are digested at varying rates, the actual number of units required for a complete digestion will change from substrate to substrate. Check individual restriction enzyme information before extending reaction times, as those that exhibit star activity should be used under recommended conditions to inhibit noncanonical cleavage. Q: Do degenerate recognition sites need to be palindromic? A: Most restriction enzyme recognition sites are palindromic and include only specified base pairs (i.e., EcoRI recognizes GAATTC). However, some enzymes have degenerate sites, meaning that they contain one or more base pairs that are not specifically defined (i.e., BsrFI-v2 recognizes RCCGGY, where R= A or G and Y= C or T). For degenerate enzymes, any base represented by the single letter code may be present at either location in the recognition site for cleavage to occur. For example, BsrFI-v2 recognizes all of the following sequences: ACCGGC, ACCGGT, GCCGGC, GCCGGT. Q: What does HF® refer to following the name of a restriction enzyme? A: HF® stands for high fidelity. Many restriction endonucleases are capable of cleaving sequences which are similar but not identical to their defined recognition sequence. This altered or relaxed specificity has been termed star activity. HF restriction endonucleases have been engineered to cleave with higher fidelity than the wild type enzyme, hence exhibiting less star activity. Screens using increased glycerol concentration, increased reaction time and high enzyme concentration were used to identify enzymes that would offer the highest fidelity over a wide range of conditions In addition, all HF enzymes are supplied with rCutSmart Buffer™ as well as a free vial of Purple Loading Dye. Learn more about High Fidelity Restriction Enzymes here. Q: Do I have to set-up digests with Time-Saver™ qualified enzymes for 5-15 minutes? Can I digest longer? A: NEB's Time-Saver™ enzymes have the benefit of working fast (5-15 minutes), but are also designed and qualified to withstand overnight digestions without degradation of DNA. Q: Can Gel Loading Dye, Purple 6X (B7024) be stored in cold temperatures? A: The recommended storage temperature for Gel Loading Dye, Purple 6X, is room temperature (25°C). Commonly, the SDS may precipitate out of solution when the dye is stored on cold temperatures. This slight precipitate can be dissipated by letting the vial sit at room temperature for an hour, or warming gently for 10 minutes. Mix the vial a few times before use, to bring the solution back to homogeneity. Q: What does it mean to be Time-Saver™ qualified? A: Enzymes that are Time-Saver qualified will digest unit assay substrate in 5-15 minutes under recommended reaction conditions, and can also be used safely in overnight digestions. Q: Which NEB restriction enzymes are supplied with Gel Loading Dye, Purple (6X)? A: All HF-restriction enzymes and most NEB non-HF restriction enzymes are supplied with Gel Loading Dye, Purple (6X). The non-HF restriction enzymes that come supplied with purple dye are: AatII AsiSI BsmBI-v2 EagI MboI NlaIII PvuI SmaI Acil AvrII BspHI EcoRI MboII NotI RsaI SpeI AfeI BamHI BsrGI EcoRV MluI NspI SacI StuI AflII BbsI ClaI Esp3I FseI MseI PacI SacII AgeI BglII DdeI HaeIII MspI PciI SalI XbaI AluI BsaI DpnI HindIII NcoI PmeI SapI XhoI ApaI BseYI DpnII HpaI NdeI PsiI-v2 SfaNI XmaI ApeKI BsiWI DraI KpnI NheI PstI SfiI XmnI AscI * All HF restriction enzymes are also supplied with Gel Loading Dye, Purple (6X) Q: Is this enzyme sensitive to dam, dcm or mammalian CpG methylation? A: Yes. This enzyme cannot cut recognition sites in mammalian gDNA that are blocked by CpG methylation. For up-to-date information about methylation sensitivities, please visit Dam-Dcm and CpG Methylation or REBASE. Q: Can you tell me more about the switch from BSA to Recombinant Albumin (rAlbumin) in NEBuffers? A: NEB is excited to announce that we have switched BSA-containing reaction buffers (NEBuffer 1.1, 2.1, 3.1 and CutSmart® Buffer) to Recombinant Albumin-containing buffers (NEBuffer r1.1, r2.1, r3.1 and rCutSmart™ Buffer). We are also in the process of moving all restriction enzyme formulations to contain rAlbumin. We feel that moving away from animal-containing products is a step in the right direction and are able to offer this enhancement at the same price. Q: Is Gel Loading Dye, Purple (6X) or Gel Loading Dye, Purple (6X), no SDS compatible with other DNA binding dyes such as SYBR® and GelRed™ during gel electrophoresis? A: Because high affinity nucleic acid binding dyes can affect DNA migration during electrophoresis, post-staining of gels with SYBR or GelRed dyes is highly recommended. However, these dyes can also be used as precast dyes (into the agarose gel). Because the Gel Loading Dye, Purple (6X) has an increased concentration in SDS, some interference may be observed when using SYBR or GelRed as precast dyes. When using these dyes as precast dyes, NEB recommends using our Gel Loading Dye, Purple, No SDS (6X) (NEB #B7025S ) instead. Please follow the recommendations below for both Purple dyes when using SYBR dyes as precast dyes: Reduce the amount of sample DNA loaded to 250 to 500ng, and use 0.5X only of SYBR dyes in precast gels. These dyes are much more sensitive than EtBr. Blown out or smeared bands can be caused by overloading. If using Gel Loading Dye, Purple (6X) B7024S , use TBE instead of TAE buffer, as the SDS interference is increased when using TAE buffer (in the gel and as a running buffer). Use the SYBR dyes as recommended by the manufacturer: add the SYBR dye to the TBE buffer first, then add the SYBR dye/TBE mix to the molten agarose solution. It is preferable to wait a few minutes to add the SYBR dyes to the molten agarose. Adding it to a cooled agarose solution (above gelling temperature, 45°C) produces better results. Always run a freshly made agarose gel, for a single run only. Re-running the gel will yield poor result. Please follow the recommendations below for both Purple dyes when using GelRed dyes as precast dyes: Reduce the amount of sample DNA loaded to 60 to 125ng, and use 0.5X only of GelRed dye in precast gels. This dye is much more sensitive than EtBr. Blown out or smeared bands can be caused by overloading. It is preferable to wait a few minutes to add the GelRed dye to the molten agarose. Adding it to a cooled agarose solution (above gelling temperature, 45°C) produces better results. Always run a freshly made agarose gel, for a single run only. Re-running the gel will yield poor result. SYBR® is a registered trademark of Life Technologies Corporation GelRed™ is a trademark of Biotium