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Time-Saver qualified Enzymes

red arrowOverview             red arrowAdvantages             red arrowProducts   

Over 200 of our enzymes are Time-Saver Qualified and will digest 1 µg of DNA in 5-15 minutes. Look for the Time-Saver icon on our web site.

At NEB, enzyme production is linked to basic research in the cloning and overexpression of restriction-modification systems. This focus allows us to provide extremely pure enzymes at concentrations that deliver more flexibility to your experimental design.

Whether you are quickly screening large numbers of clones or setting up overnight digests, you will benefit from the high quality of our enzymes. Typically, a restriction digest involves the incubation of 1 µl of enzyme with 1 µg of purified DNA in a final volume of 50 µl for 1 hour. However, to speed up the screening process, choose one of NEB's enzymes that are Time-Saver qualified. These enzymes will digest 1 µg of substrate DNA in 5-15 minutes using 1 µl of enzyme under recommended reaction conditions. Unlike other suppliers, there is no special formulation, change in concentration or need to buy more expensive new lines of enzymes to achieve digestion in 5-15 minutes. In fact, 84% will fully digest 1 µg of DNA in 15 minutes or less (see table). That means over 200 of our restriction enzymes have the power to get the job done fast.

In an effort to provide you with as much information as possible, NEB has tested all of its enzymes on unit assay substrate as well as plasmid substrate. By definition, Time-Saver qualified restriction enzymes digest unit assay substrate in 5-15 minutes. The rate of cutting for plasmid substrate is also given; however, we recommend that this be used as a guide and is not definitive for all plasmids. Restriction enzymes can often show site preference, presumably determined by the sequence flanking the recognition site. In addition, supercoiled DNA may have varying rates of cleavage.

Since all of our enzymes are rigorously tested for nuclease contamination, you can also safely set up digests for long periods of time without sample degradation. Only NEB can offer enzymes with power and purity — the power to digest in 5-15 minutes and the purity to withstand overnight digestions with no loss of substrate.

Advantages:
  • Enzymes powerful enough to digest in 5-15 minutes
  • Pure enough for overnight incubation
  • No special formulation
  • No added expense
Power and purity of Time-Saver qualified enzymes:
HindIII is powerful enough to digest 1 µg of DNA in 5 minutes, but can also be used in overnight digests with no indication of nuclease contamination. Marker (M) is the 1 kb DNA Ladder (NEB #N3232).

Recombinant Digest in 5 minutes
Enzymes that are Time-Saver qualified will digest unit assay substrate in 5-15 minutes under recommended reaction conditions Digest in 15 minutes
  Not completely digested in 15 minutes
  NT Not tested.
     


EnzymeSequenceRecom-binantTime-Saver QualifiedUnit Assay SubstratePlasmid Substrate
 AatIIGACGT/C  
 Acc65IG/GTACC  
 AccIGT/MKAC  
 AciICCGC(-3/-1)  
 AclIAA/CGTT  
 AcuICTGAAG(16/14)  
 AflIIC/TTAAG  
 AgeIA/CCGGT  
 AgeI-HF™A/CCGGT  
 AgeI-HF™ RE-Mix™A/CCGGT  
 AhdIGACNNN/NNGTC  
 AluIAG/CT  
 AlwIGGATC(4/5)  
 AlwNICAGNNN/CTG  
 ApaIGGGCC/C  
 ApaLIG/TGCAC  
 ApeKIG/CWGC  
 ApoIR/AATTY  
 AscIGG/CGCGCC  
 AscI RE-Mix™GG/CGCGCC  
 AseIAT/TAAT  
 AsiSIGCGAT/CGC  
 AvaIC/YCGRG  
 AvaIIG/GWCC  
 AvrIIC/CTAGG  
 BaeGIGKGCM/C 
 BaeI(10/15)ACNNNNGTAYC(12/7) 
 BamHIG/GATCC  
 BamHI-HFG/GATCC  
 BanIIGRGCY/C  
 BbsIGAAGAC(2/6) 
 BbvCICCTCAGC(-5/-2)  
 BbvIGCAGC(8/12)  
 BccICCATC(4/5)  
 BceAIACGGC(12/14)  
 BciVIGTATCC(6/5)  
 BclIT/GATCA  NT
 BcoDIGTCTC(1/5)  
 BfaIC/TAG 
 BfuAIACCTGC(4/8) 
 BfuCI/GATC  
 BglIGCCNNNN/NGGC  
 BglIIA/GATCT  
 BlpIGC/TNAGC  
 BmgBICACGTC(-3/-3)  
 BmrIACTGGG(5/4)  
 BpmICTGGAG(16/14)  
 BpuEICTTGAG(16/14)  
 BsaAIYAC/GTR  
 BsaBIGATNN/NNATC 
 BsaHIGR/CGYC  
 BsaI-HF™GGTCTC(1/5)  
 BsaWIW/CCGGW  
 BsaXI(9/12)ACNNNNNCTCC(10/7) 
 BseRIGAGGAG(10/8)  
 BsgIGTGCAG(16/14) 
 BsiEICGRY/CG 
 BsiWIC/GTACG  
 BslICCNNNNN/NNGG  
 BsmAIGTCTC(1/5)  
 BsmBICGTCTC(1/5)  
 BsmFIGGGAC(10/14)  
 BsmIGAATGC(1/-1)  
 BsoBIC/YCGRG  
 Bsp1286IGDGCH/C 
 BspCNICTCAG(9/7) 
 BspEIT/CCGGA  
 BspHIT/CATGA  
 BspQIGCTCTTC(1/4)  
 BsrBICCGCTC(-3/-3) 
 BsrDIGCAATG(2/0) 
 BsrFIR/CCGGY  
 BsrGIT/GTACA  
 BsrIACTGG(1/-1) 
 BssHIIG/CGCGC  
 BssKI/CCNGG  
 BstBITT/CGAA  
 BstEIIG/GTNACC  
 BstEII-HF™ RE-Mix™G/GTNACC  
 BstNICC/WGG  
 BstUICG/CG 
 BstXICCANNNNN/NTGG  
 BstYIR/GATCY  
 BstZ17IGTA/TAC 
 Bsu36ICC/TNAGG  
 BtgIC/CRYGG  
 BtsCIGGATG(2/0)  
 BtsIGCAGTG(2/0)  
 Cac8IGCN/NGC 
 ClaIAT/CGAT  
 CspCI(11/13)CAANNNNNGTGG(12/10)  
 CviAIIC/ATG  
 CviKI-1RG/CY  
 CviQIG/TAC  
 DdeIC/TNAG  
 DpnIGA/TC  
 DpnII/GATC  
 DraITTT/AAA  
 DraIIICACNNN/GTG  
 DraIII-HF™CACNNN/GTG  
 DrdIGACNNNN/NNGTC 
 EagIC/GGCCG  
 EagI-HFC/GGCCG  
 EarICTCTTC(1/4)  
 EcoNICCTNN/NNNAGG  
 EcoO109IRG/GNCCY  
 EcoP15ICAGCAG(25/27)  
 EcoRIG/AATTC  
 EcoRI-HFG/AATTC  
 EcoRVGAT/ATC  
 EcoRV-HF™ RE-Mix™GAT/ATC  
 EcoRV-HFGAT/ATC  
 Fnu4HIGC/NGC  
 FokIGGATG(9/13)  
 FseIGGCCGG/CC  
 FspITGC/GCA  
 HaeIIRGCGC/Y  
 HaeIIIGG/CC  
 HgaIGACGC(5/10)  
 HhaIGCG/C  
 HincIIGTY/RAC  
 HindIIIA/AGCTT  
 HindIII-HF™A/AGCTT  
 HinfIG/ANTC  
 HinP1IG/CGC  
 HpaIGTT/AAC  
 HpaIIC/CGG  
 HphIGGTGA(8/7)  
 Hpy166IIGTN/NAC  
 Hpy188ITCN/GA  
 HpyAVCCTTC(6/5)  
 HpyCH4IVA/CGT  
 HpyCH4VTG/CA  
 KpnIGGTAC/C  
 KpnI-HF™GGTAC/C  
 KpnI-HF™ RE-Mix™GGTAC/C  
 MboI/GATC  
 MboIIGAAGA(8/7)  
 MfeIC/AATTG  
 MfeI-HF™ RE-Mix™C/AATTG  
 MfeI-HFC/AATTG  
 MluCI/AATT  
 MluIA/CGCGT  
 MlyIGAGTC(5/5)  
 MmeITCCRAC(20/18)  
 MnlICCTC(7/6)  
 MseIT/TAA  
 MslICAYNN/NNRTG  
 MspA1ICMG/CKG  
 MspIC/CGG  
 MwoIGCNNNNN/NNGC  
 NciICC/SGG  
 NcoIC/CATGG  
 NcoI-HF™ RE-Mix™C/CATGG  
 NcoI-HFC/CATGG  
 NdeICA/TATG  
 NgoMIVG/CCGGC  
 NheIG/CTAGC  
 NheI-HF™ RE-Mix™G/CTAGC  
 NheI-HFG/CTAGC  
 NlaIIICATG/  
 NmeAIIIGCCGAG(21/19)  
 NotIGC/GGCCGC  
 NotI-HF™ RE-Mix™GC/GGCCGC  
 NotI-HFGC/GGCCGC  
 NruITCG/CGA  
 NsiIATGCA/T  
 NspIRCATG/Y  
 PacITTAAT/TAA  
 PacI RE-Mix™TTAAT/TAA  
 PaeR7IC/TCGAG  
 PflFIGACN/NNGTC 
 PflMICCANNNN/NTGG  
 PmeIGTTT/AAAC  
 PmlICAC/GTG 
 PpuMIRG/GWCCY  
 PshAIGACNN/NNGTC  
 PstICTGCA/G  
 PstI-HF™CTGCA/G  
 PvuICGAT/CG  
 PvuI-HF™CGAT/CG  
 PvuIICAG/CTG  
 PvuII-HFCAG/CTG  
 RsaIGT/AC  
 SacIGAGCT/C  
 SacI-HFGAGCT/C  
 SacIICCGC/GG  
 SalIG/TCGAC  
 SalI-HF™ RE-Mix™G/TCGAC  
 SalI-HFG/TCGAC  
 SapIGCTCTTC(1/4)  
 SbfICCTGCA/GG  
 SbfI-HFCCTGCA/GG  
 ScaIAGT/ACT  
 ScaI-HF™ RE-Mix™AGT/ACT  
 ScaI-HFAGT/ACT  
 ScrFICC/NGG  
 SfiIGGCCNNNN/NGGCC  
 SfoIGGC/GCC  
 SmaICCC/GGG  
 SnaBITAC/GTA  
 SpeIA/CTAGT  
 SpeI RE-Mix™A/CTAGT  
 SphIGCATG/C  
 SphI-HFGCATG/C  
 SspIAAT/ATT  
 SspI-HFAAT/ATT  
 StuIAGG/CCT  
 StyD4I/CCNGG  
 StyIC/CWWGG  
 StyI-HF™C/CWWGG  
 SwaIATTT/AAAT  
 TaqαIT/CGA  
 TfiIG/AWTC  
 TseIG/CWGC 
 Tsp509I/AATT  
 TspMIC/CCGGG 
 TspRINNCASTGNN/  
 Tth111IGACN/NNGTC  
 XbaIT/CTAGA  
 XbaI RE-Mix™T/CTAGA  
 XcmICCANNNNN/NNNNTGG  
 XhoIC/TCGAG  
 XhoI RE-Mix™C/TCGAG  
 XmaIC/CCGGG  
 XmnIGAANN/NNTTC  



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