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Product insert

A technical challenge with this step is to achieve RNA extraction of uniform quality and efficiency for each fraction. This is because the amount of RNA in each sucrose gradient fraction varies considerably and the high concentration of sucrose in the bottom fractions interferes with phase separation in typical phenol-based extraction steps. To address these problems, we spike each fraction with an aliquot of a foreign (control) RNA, which can be used later to correct for differences in RNA recovery (and reverse transcription efficiency) between samples. We then remove sucrose from the samples by precipitation of total nucleic acid and protein with ethanol. To purify RNA, a standard Trizol (Invitrogen) extraction is performed as outlined later (also see product insert). [Pg.137]

Continue with standard Trizol extraction (see product insert). [Pg.138]

Wyeth-Ayerst Laboratories and Immunex Inc. Etanercept (Enbrel ) Product Insert, 2006. [Pg.137]

Biogen IDEC. Alefacept (Amevive ) Product Insert, 2005. [Pg.141]

Boehringer Mannheim product insert for anti-digoxigenin-POD, Fab fragments. (1995) Boehringer Mannheim, Hanover, Germany. [Pg.200]

Tetanus immune globnlin (hnman) solvent/ detergent treated [FDA fnll name on product insert]... [Pg.524]

The product insertion port is usually a tray or a manifold where the frozen product is placed for freeze-drying. [Pg.23]

Polymerization of isocyanides is a thermodynamically feasible process, in agreement with the stoichiometric multiple insertion observed in reactions between metal-alkyl complexes and isocyanides. The entropy loss in the case of isocyanides is lower than for insertion of CO. Isocyanide insertions into palladium-alkyl a bonds are faster than those for the platinum(II) analogues. The latter, on the other hand, usually lead to more stable and better defined products. Insertion of isocyanides into platinum-carbon bonds has been studied extensively Reaction (j) is typical the ionic product was strongly suggested by observation that the compounds isolated under mild conditions are 1 1 electrolytes. [Pg.645]

Compendium of Pharmaceuticals and Specificities (CPS) Manual Drug reference for health professionals that provides lists of drugs by generic names and trade names with the manufacturer s product insert reproduced. The manuel includes a therapeutic guide, manufacturer s index, drug listing by... [Pg.516]

Strip packaging machines are far simpler and smaller than blister packaging units, usually simply consisting of a feed system, product insertion plus heat sealing, and a guillotining operation to size. [Pg.374]

Irradiation of azidosilacyclopentanes and azidosilacycloheptanes in the presence of tert-butyl alcohol or trimethoxymethylsilane yields adducts derived from both expected silanimine products insertion products of the corresponding nitrenes into C-H bonds are obtained as well349. The authors propose that a concerted mechanism for N2 loss and concurrent bond shift and a stepwise mechanism involving a discrete nitrene intermediate are both operational. [Pg.1112]

Dihydropyrroles and indoles. The salt reacts with tosylamide anions to provide five-membered heterocycles via carbene intermediates. When a nucleofugal group (methoxy is sufficient) is present at the bond insertion point, automatic elimination gives a pyrrole as the product. Insertion into an aryl C-H bond leads to an indole. [Pg.270]

This information is available in product inserts, various drag handbooks for nurses, and in computerized pharmacology databases and in the following ... [Pg.35]

CD4 T cell count Treatment initiatimr is contraindieated in males with CD4 T eell eormts >400 cells mm and in females > 250 cells rrrm Nevirapine Product Insert... [Pg.440]

To decrease the incidence of skin rash in patients, a tolerance induction regime was established in patients 200 mg of nevirapine is administered daily for the first 2 weeks, followed by the full therapeutic dose of 200 mg twice daily. This regime successfully decreases the rash incidence by about 50% (Nevirapine product insert). In rats, daily treatment with 40 or 75 mg/kg/day of nevirapine for the first 2 weeks followed by 150 mg/kg/day (a dose that otherwise leads to a 100% incidence of rash) completely prevents the skin rash (Shenton et al. 2005). [Pg.443]

Pd(COMe)(Cl)(6-Mebipy)], which on interaction with NaB(C6H3(CF3)2-3 )4 yields [Pd(Me)(CO)(6-Mebipy)] B(C6H3(CF3)2-3,5)4 (01OM4111). The product inserts ethylene to yield 56. [Pg.68]

The following near-term, lower risk applications represent product insertions that could provide long-term experience with CMCs ... [Pg.32]

Content, molecular weight, pH-value, buffer substance and osmolality should all be included by the manufacturer in the product insert. [Pg.16]

There are (n + 1) of these products inserting the recurrence relation, Eq. 3.48, shows... [Pg.112]

The next step in cloning is the transformation of competent Escherichia coli host cells. These can be prepared in-house through electroporation or chemical treatments (e.g., calcium chloride or rubidium chloride) or ordered from a vendor separately or as part of a cloning kit. The least expensive approach is to prepare the competent cells in-house, but this involves a trade-off in time. The expense of vendor-purchased cells can be reduced by using half the recommended volume per transformation, which works fine unless there are too few transformants recovered. (For example, we have had this experience using the TOPO-based veetor and long PCR product inserts.) The manufacturer s transformation instructions can be followed directly. For the transformation of chemically competent One Shot E. coli, this entails the following steps, for a half-volume transformation ... [Pg.70]

The patch adheres to the skin and when it is exposed to air, the contained heating element is activated and through oxidation releases heat. Local skin temperature remains between 39 and 41°C during the heating phase of application. Systemic absorption is minimal and even with sequential or simultaneous applications of up to four patches, lidocaine plasma levels were low (9-12 ng/mL in adults) and tetracaine levels were essentially non-detectable. The product insert indicates that application of one Synera patch for up to 30 minutes in children 4 months to 12 years of age produced maximum peak plasma concentrations of lidocaine and tetracaine of 63 ng/ mL and 65 ng/mL, respectively. Application of two Synera patches for up to 30 minutes to children 4 months to 12 years of age produced peak lidocaine levels of up to 331 ng/mL and tetracaine levels of less than 5 ng/mL. [Pg.286]


See other pages where Product insert is mentioned: [Pg.68]    [Pg.130]    [Pg.137]    [Pg.137]    [Pg.141]    [Pg.424]    [Pg.433]    [Pg.28]    [Pg.218]    [Pg.68]    [Pg.804]    [Pg.2831]    [Pg.746]    [Pg.418]    [Pg.155]    [Pg.284]    [Pg.326]    [Pg.571]    [Pg.573]    [Pg.439]    [Pg.148]    [Pg.321]    [Pg.1145]    [Pg.62]    [Pg.1059]    [Pg.68]    [Pg.293]    [Pg.417]    [Pg.45]   
See also in sourсe #XX -- [ Pg.16 ]




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