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Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
WesternBright Sirius is the most sensitive HRP substrate available from Advansta for chemiluminescent Western blotting. With attomole sensitivity and a long-lasting signal, WesternBright Sirius allows you to detect bands not visualized with other substrates. High signal-to-noise and a large dynamic range make it ideal for quantifying low-intensity bands.
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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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Human CYP2C91 + P450 Reductase + Cytochrome b5 SUPERSOMES 0.5 nmole cytochrome P450 in 0.5mL This activity is catalyzed by CYP2C91 expressed from human CYP2C91 cDNA using a baculovirus expression system
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Recombinantly produced in E. coli, CUTANA pAG-Tn5 for ChIC/CUT&Tag is a fusion of Proteins A and G to Transposase Tn5. This construct is useful in performing Cleavage Under Targets and Tagmentation (CUT&Tag). The active dimer of Transposase Tn5 is charged with Illumina adapters and ready to be used immediately in CUT&Tag. CUTANA pAG-Tn5 does not contain an epitope tag, which makes it compatible with tag-mediated CUT&Tag.
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Diaphorase, Code: DILW, Store at 2 deg. to 8 deg.C, Minimum activity: 30U/mg dry weight, Supplied as a dialyzed, lyophilized powder, Unit Definition: 1 Unit equals a decrease in absorbance at 600nm of 1.0 per minute at 25 deg.C, pH 7.5, 1kU
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Type XIV, ≥3.5 units/mg solid, powder, Synonym: Actinase E, Pronase E. Highly stable in pH range of 5.0 to 9.0, with peak activity at pH 8.8. Compatible with many DNA and RNA isolation buffers. Broad substrate specificity.
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