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Filtered Search Results
ABclonal Technology SfiI
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5…GGCCNNNN/NGGCC...3 3…CCGGN/NNNNCCGG...5
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Supply Solutions Roche - High Fidelity PCR Master
Roche - High Fidelity PCR Master
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ABclonal Technology BstBI
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5...T T/ C G A A...3 3...A A G C/ T T...5 Isoschizomers: Bsp119I AsuII Bpu14I BspT104I NspV SfuI
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New England Biolabs, Inc. APE 1 – 1000 units
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Human apurinic/apyrimidinic (AP) endonuclease, APE 1, also known as HAP 1 or Ref-1, shares homology with Escherichia coli exonuclease III protein. APE 1 cleaves the phosphodiester backbone immediately 5 to an AP site, via hydrolytic mechanism, to generate a single-strand DNA break leaving a 3-hydroxyl and 5-deoxyribose phosphate terminus. Besides AP endonuclease activity, APE 1 has also been reported to have weak DNA 3 -diesterase, 3 to 5 exonuclease and RNase H activities (3-5). In addition to DNA repair activity, APE 1 is also capable of regulating the DNA binding activity of many transcription factors in vitro by a redox mechanism. As part of this process, APE 1 has been shown to stimulate the DNA binding activity of Fos-Jun heterodimers, Jun-Jun homodimers and Hela cell AP-1 proteins as well as that of several other transcription factors including NF-kB, Myb and members of the ATF/CREB family.
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New England Biolabs, Inc. XbaI – 3000 units
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A restriction endonuclease that recognizes the sequence T^CTAG_A.
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New England Biolabs, Inc. I-CeuI – 500 units
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A restriction endonuclease that recognizes the sequence CGTAACTATAACGGTC_CTAA^GGTAGCGAA.The intron encoding I-CeuI is present in the chloroplast large rRNA gene of Chlamydomonas eugametos (1). This gene has been cloned and overexpressed in E. coli (2).
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New England Biolabs, Inc. SacI-HF – 10000 units
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A high fidelity restriction endonuclease that recognizes the sequence G_AGCT^C. High Fidelity (HF) Restriction Enzymes have 100% activity in rCutSmart Buffer; single-buffer simplicity means more straightforward and streamlined sample processing. HF enzymes also exhibit dramatically reduced star activity. HF enzymes are all Time-Saver qualified and can therefore cut substrate DNA in 5-15 with the flexibility to digest overnight without degradation to DNA. Engineered with performance in mind, HF restriction enzymes are fully active under a broader range of conditions, minimizing off-target products, while offering flexibility in experimental design. NEB extensively performs quality controls on all standard and high-fidelity (HF) restriction enzymes.
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New England Biolabs, Inc. EnGen Spy Cas9 Nickase – 70 pmol
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EnGen Spy Cas9 Nickase is a variant of Cas9 nuclease differing by a point mutation (D10A) in the RuvC nuclease domain, which enables it to nick, but not cleave, DNA). EnGen Spy Cas9 Nickase, like EnGen Cas9 NLS , targets DNA using a guide RNA complementary to a site with a 3' NGG protospacer adjacent motif (PAM). Nicking occurs on the DNA strand opposite the PAM. Double-stranded DNA breaks can be generated with reduced off-target cleavage by targeting two sites in close proximity (generally 0-20 bp apart) and with PAMs facing outward to leave 5' overhangs. Nicking by EnGen Spy Cas9 Nickase occurs on the DNA strand opposite the target sequence. EnGen Spy Cas9 Nickase contains SV40 T antigen nuclear localization (NLS) sequences on the N and C- termini.
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| Components | 25 to 50% Water, >50% Glycerin |
|---|---|
| Cut Site | GC.GGCCGC |
| Content And Storage | Keep container tightly closed |
| Form | Liquid |
| Product Type | NotI |
| Storage Buffer | 20mM Tris HCl (pH 7.8 at 25°C), 100mM NaCl, 0.1mM EDTA, 1mM DTT, 0.02% Triton™ X-100, 0.2mg/mL BSA, 50% Glycerol |
| pH | 7.4 |
| Concentration | 10 U/μL |
| For Use With (Application) | >90% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with Not I |
| Components | 25 to 50% Water, >50% Glycerin, 1 to 2.5% Potassium Chloride |
|---|---|
| Cut Site | A.AGCTT |
| Content And Storage | Keep container tightly closed |
| Form | Liquid |
| Product Type | HindIII |
| Storage Buffer | 10mM Tris HCl (pH 7.5 at 25°C), 250mM KCl, 1mM DTT, 0.1mM EDTA, 0.2mg/mL BSA, 50% Glycerol |
| Incubator Temperature | 37°C |
| Concentration | 10 U/μL |
| For Use With (Application) | >95% of DNA fragments can be ligated and re-cut after 50-fold over-digestion with HaeIII |
| Components | 10X OPTIZYME™ Buffer 4 |
|---|---|
| Cut Site | T.CTAGA |
| Form | Liquid |
| Product Type | XbaI |
| Storage Buffer | 10mM Tris HCl (pH 7.4), 100mM KCl, 7mM 2-mercaptoethano, 1mM EDTA, 0.2mg/mL BSA, 50% Glycerol |
| pH | 7.4 |
| Incubator Temperature | 37°C |
| For Use With (Application) | Indicates ligation efficiency of DNA fragments generated by digestion with the Restriction Enzyme |
| Components | 25 to 50% Water, >50% Glycerin |
|---|---|
| Cut Site | C.TNAG |
| Content And Storage | Keep container tightly closed |
| Form | Liquid |
| Storage Buffer | 10mM Tris HCl (pH 7.4 at 25°C), 100mM KCl, 1mM DTT, 1mM EDTA, 0.2mg/mL BSA, 50% Glycerol |
| pH | 7.4 |
| Incubator Temperature | 37°C |
| Concentration | 10 U/μL |
| For Use With (Application) | >95% of DNA fragments can be ligated and re-cut after 50-fold over-digesiton with DdeI |