Buffer stock

National Defense Stockpile Goal for tin at 42,700 metric tons. On January 2, 1980, the Strategic and Critical Materials Transaction Authorization Act became effective. This authorizes the President to dispose of materials determined to be excessive to the current needs of the stockpile. This act provides for the sale of up to 35,600 metric tons of tin, including a contribution of up to 5100 metric tons of tin to the International Tin Council (ITC) buffer stock (see below). The GSA set up a schedule to offer about 500 metric tons of Grade A tin, for domestic sales and consumption only, every other Tuesday beginning July 1, 1980. On December 14, 1981, the restrictions on exporting the GSA tin sold were lifted sales increased immediately. Thus, from July 1, 1980, through December 11, 1981, the total GSA sales were 3170 metric tons. An additional 1815 metric tons were sold soon thereafter, mostiy to traders (10). [Pg.59]

A buffered stock solution of the complex was prespotted on the tab. The dry tab with preimmobilized E5-Ab complex was then utilized to perform the assay. b At the time of assay a buffered stock solution of the complex was spotted on the tab either by itself or as a mixture with the analyte depending on the specific assay format. [Pg.470]

Cell lysis buffer stock solution (lOx) 1.21 g Tris base (pH 7.4), 4.39 g NaCl, 0.19 g ethylenediaminetetraacetic acid (EDTA), 0.19 g ethylene glycol tetraacetic acid (EGTA),... [Pg.76]

Sodium dodecyl sulfate (SDS) sample buffer stock solution Dissolve 1.51 g Tris base to 15 ml of distilled water, and then add 25 ml of 50% glycerol into the mixture. Stir to dissolve and then adjust pH to 6.8 with HCl. Dissolve 5 g of SDS in this buffer and make up to 50 ml with distilled water. Dissolve 0.01 g of bromophenol blue and stir overnight. [Pg.76]

SDS-PAGE transfer buffer stock solution (lOx) Weigh 30.30g Tris base, 144.0 g glycine. Make up to 1,000 ml with distilled water. [Pg.77]

Add 5 pi of2-mercaptoethanol to 95 pi of SDS sample buffer stock solution to give a sample buffer mixture. (SDS may precipitate at room temperature. Warm up the SDS sample buffer stock solution before use) (see Note 8). [Pg.78]

If buffer stock solutions are used, adjust them in a way that the working dilution has the right pH (pH mostiy increases when buffers are diluted). [Pg.201]

Concentrated (e.g. 5 x) buffer stock solutions are made up, and diluted for use both in the gels and reservoirs. The following buffers originally employed by Loening (1967) are commonly used, but numerous others are equally suitable ... [Pg.368]

A variety of pH 7.0 buffered, stock solutions of urea at various concentrations are prepared. The concentrations of urea chosen are such that the complete kinetic profile of the reaction can be observed (i.e. from first-order through mixed-order and finally to zero-order kinetics). [Pg.117]

M Sorenson s phosphate buffer Stock Dissolve 7.176 g sodium phosphate monobasic monohydrate (NaH2P04-H20) in 100 mL distilled H20. Dissolve 49.4 g of sodium phosphate (NaP04) in 750 mL distilled H20. Mix the sodium phosphate monobasic monohydrate and sodium phosphate solutions in a 1 L cylinder. Bring volume to 1 L with distilled water. The pH should be 7.6. Do not adjust pH. This may be stored at room temp for up to 6 months. For use dilute with distilled water to 0.1 M. [Pg.57]

You want to maintain electric equivalence, so you do not use holes next to each other. Use holes opposite to each other as much as possible. Examine the lower buffer chamber. It has a water jacket around it so that the samples can be cooled if necessary. The upper buffer and the lower buffer are separated as stock solutions, because the upper buffer has a marker dye in it that the lower one does not have. These buffers can be used again. Notice on the buffer stock solutions that the label tells how many people have used them. You can use this solution four different times before you have to change it. Please initial the label, showing that you have used it. Fill the lower buffer chamber to within 1 cm of the rim. [Pg.650]

Ab Microarray Buffer Kit (Cat. No. 631792, Clontech, Mountain View, CA, USA) containing, Incubation Tray, Extraction/Labeling Buffer, Stock Incubation Buffer, Background Reducer, and Wash Buffers A-C. [Pg.178]

Preincubate sections (10 min) in DAB substrate with nickel (Ni) solution without hydrogen peroxide (H2O2). To prepare, use the DAB substrate kit (Vector Laboratories, Burlingame, CA). Add two drops buffer stock to 5 mL of distilled water and mix. Add four drops DAB stock solution and mix. Add two drops of nickel solution and mix. [Pg.60]

Buffers, Stock Solutions, and Reagents for Fractionating Rat liver... [Pg.9]

We prepare a stock solution of 2.2% n-propyl gallate in 100% glycerol (mix overnight at room temperature), and then add one-tenth volume of a lOx buffer stock. [Pg.55]

Stock solutions of these dyes are prepared by dissolving 1 mg of dye in 1 ml methanol (stock A), and diluting an aliquot of this stock to 20 /ig/ml in egg lysis buffer (stock B). These solutions can be stored for up to 3 months in the dark at 4°C without loss of activity. [Pg.432]

Nuclear-associated vesicles (either chromatin-bound or fused into an envelope) can be labeled. Alternatively, vesicles can be prelabeled prior to nuclear assembly reactions. To label chromatin-associated vesicles, a 10-/il extract containing nuclei is mixed with 10 ju.1 of DiOC6 or DilCis, each at 20 /xg/ml in egg lysis buffer (stock B), and incubated at room temperature for 20 min. Samples are visualized under the fluorescence microscope using the appropriate filter sets. Nuclear DNA can be simultaneously labeled at a final concentration of 0.1 /u.g/ml Hoechst 33342. If desired, samples can be fixed and stained simultaneously. A IO-/1I sample is mixed with 10 /x.1 of 7% paraformaldehyde containing 20 ju.g/ml of either of the lipophilic dyes. [Pg.433]

How do apparel supply chains compete One approach is to compete on cost, an approach used by Walmart and other department stores. This strategy focuses on developing a cost-efficient supply chain that may require global sourcing with low costs but long lead times. Such supply chains then require large buffer stocks to compensate for demand uncertainty or a focus on predictable demand for basic products with low demand uncertainty But there are many other dimensions of competition in the apparel industry. [Pg.101]

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