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For researchers, scientists, and technical professionals: Your one-stop shop for the complete range of laboratory, production, and safety products and services.
Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
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T7 Endonuclease I (T7EI) is a recombinant DNA endonuclease produced through expression in E coli T7EI specifically targets and cleaves diverse forms of DNA substrates containing structural anomalies including mismatches of at least two base pairs heteroduplex DNA cruciform structures Holliday junctions and branched DNA intermediates as well as nicked duplexes at reduced cleavage efficiency It hydrolyzes phosphodiester bonds located near mismatched nucleotides 5 ends This enzyme is widely employed in detecting genetic mutations induced by gene-editing systems (e g CRISPR/Cas9 TALENs) identifying single nucleotide polymorphisms (SNPs) and generating randomized DNA fragments for shotgun cloning techniques
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Coagulation protein, Human Plasmin, 500 micrograms, Native enzyme, Mode of action: Enzyme involved in fibrinolysis, Research use only, 50% (v/v) glycerol/water, store at -20 Celsius.
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Xanthine Oxidase Grade II (Lyophilized Powder) consists of a highly purified native Xanthine oxidase supplied as a lyophilized form Xanthine oxidase uses molybdenum as cofactor and plays a central role in the metabolism of nucleotides It is extensively used in enzymatic assays for the determination of inorganic phosphorus 5-nucleotidase (5-NT) and adenosine deaminase (ADA) For in vitro research use only
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DNA Ligase 4 Primary Antibody Unconjugated Public Immunogen Range 504-685/911 Host Species Rabbit Target Species Human Clonality Monoclonal Applications WB FCM IC Concentration Lot dependent Size 50 ul Storage Buffer Supplied in PBS (pH 7 4) containing 50% glycerol and 0 02% sodium azide
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ADAMTS-5 inhibitor is a small-molecule research compound that selectively inhibits ADAMTS-5 (aggrecanase-2) with an IC50 of 1.1 μM. It is supplied as a high-purity solid for biochemical and cell-based studies.
Potent ADAMTS-5 inhibition (IC50 1.1 μM).
Greater than 40-fold functional selectivity over ADAMTS-4.
High reported purity (99.59%).
Molecular weight 449.92 g/mol; formula C16H11ClF3N3OS3.
Available in mg-scale quantities for research use.
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MW 408.63 g/mol. Chromogenic substrate for β-galactosidase producing a red or magenta insoluble product. Used to determine the presence or absence of a cloned DNA insert in bacteria growing on agar plates. Designed to replace X-Gal in blue-white selection of recombinant bacterial colonies with the lac+ phenotype. Lac+ colonies grown in the presence of Magenta-Gal turn an intense red color, allowing for easy differentiation between lac+ and lac- colonies.
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T4 Phage -glucosyltransferase specifically transfers the glucose moiety of uridine diphosphoglucose (UDP-Glc) to the 5-hydroxymethylcytosine (5-hmC) residues in double-stranded DNA, making beta-glucosyl-5-hydroxymethylcytosine.
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The bacterial RNA 5' Pyrophosphohydrolase (RppH) removes pyrophosphate from the 5' end of triphosphorylated RNA to leave a 5' monophosphate RNA. The RppH protein was also known as NudH/YgdP which can split Ap5A to ADP and ATP.
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Enzyme; Micrococcal nuclease; 15,000U; Digests single-stranded DNA; Will also digest double-stranded DNA or RNA; Yield 3'-phosphate mononucleotides and oglionucleotides; Requires calcium; Completely inactivated by EDTA and EGTA
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