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Restriction enzymes, modifying enzymes, buffering solutions, inhibitors, and substrates for use in clinical, research, and general laboratory procedures.
Prepared from the 1 mM sodium pyrophosphate, pH 6.9, alumina gel eluate of Hilmoe, Biochem. Prep, 8, (Meister, A., ed.), John Wiley & Sons, NY, NY, p. 105 (1961). Lyophilized in vials. 9068-54-6
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Proteinase K is a high-activity protease enzyme used primarily in DNA and RNA extraction procedures. This enzyme is highly effective in breaking down proteins, including histones, which helps release nucleic acids from cellular and nuclear structures. Proteinase K remains active under a wide range of conditions, making it ideal for use in DNA extractions that involve detergents or other chemical treatments. This reagent is provided in a 100 mg package, suitable for larger experiments or multiple applications. It is frequently used in research labs, particularly in protocols for DNA purification, proteinase inactivation, and enzymatic assays.
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4-Methylumbelliferyl-α-D-glucopyranoside[4-Methylumbelliferyl-α-D-Glucoside]C16H18O8MW 338.3Fluorescent substrate for -α-D-Glucosidase.Purity: >98%. 4-Methylumbelliferone <50ppm.Soluble in 2% acetone/water 1:1.CAS 17833-43-1This product is sold for laboratory research use only.
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ABTS, Diammonium Salt Also known as 2,2'-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid). Technical Information:Ultra Pure GradePurity: >98.0%Em (225nm, H2O): >48.150Solubility (H2O): 5%Store: Frozen
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ABTS, Diammonium Salt Also known as 2,2'-Azino-bis(3-ethylbenzthiazoline-6-sulfonic acid). Technical Information:Ultra Pure GradePurity: >98.0%Em (225nm, H2O): >48.150Solubility (H2O): 5%Store: Frozen
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Proteinase K is a robust endopeptidase that inactivates and destroys proteins without any pronounced cleavage specificity. Consists of 100 mg of lyophilized Proteinase K (with an activity of >2.5 U/mg) plus 8 ml of a stabilizing solution (Proteinase Buffer PB).
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An active metabolite of thalidomide and a PROTAC synthetic intermediate; decreases production of TNF-α induced by TPA in THP-1 cells at 30 µM; completely inhibits the proliferation HUVECs at 333 µM; inhibits VEGF- and FGF2-induced angiogenesis by 14% in a CAM assay in utero at 100 µg/embryo
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