Orange Color Code

Assemble the peristaltic pump tubes, injector, reactor, and detector as described in the instrument operation manual or by your instructor. There will be three peristaltic pump tubes, one for the carrier (0.89 mm i.d., orange-orange color-coded stops), one for the reagent (0.89 mm i.d., orange-orange), and one for the sample (0.89 mm i.d., orange-orange). 

Assemble the flow injection apparatus in the single-line mode as described by the manufacturer or your instructor. Use 0.89-mm i.d. pump tubing for the carrier and the sampling tubes (orange-orange color-coded stops on the peristaltic punip tubing). This should provide a flow rate of about 1.15 mL/min when using 25 rpm for the peristaltic pump. 

Figure2.5 Biological fingerprint forclozapine showingthe results for assays with a percent inhibition >90% at 10 pM (upper line, red). The IC50S are shown as color coded on the lower line (red < 100 nM, orange < 1 jj,M, yellow < 5pM).

Fig. 3 Typical ICT probes (left) and representative spectroscopic responses toward selected metal ions (right). Color code (left) coordinating atoms in blue, bridgehead atom of the fluorophore that takes part in complexation in orange, formal donor fragment in red, formal acceptor fragment in green (right) hypsochromic shifts in red, bathochromic shifts in green, fluorescence enhancement in violet, fluorescence quenching in blue. Symbols in table Aabs, 7em,

Fig. 6 Typical PET probes (a) and representative fluorescence light-up responses toward selected metal ions in tabulated (b) and graphical form (c trace 1 = 14, trace 2 = 14-(Zn2+)2, trace DMA = 9,10-dimethylanthracene in MeCN). Color code coordinating atoms in blue, atoms which take part in the complexation and show (main, in 14) PET activity in orange, fluorophore in green. Lincoln and co-workers have demonstrated that the attachment of two dimethylamino groups through propylene spacers to the 9,10-positions of anthracene has a more than 100-fold weaker PET activity than the attachment through methylene spacers [62]. The blue N atoms in 14 are thus predominantly responsible for coordination. For symbols, see Fig. 3. Quantum yield of 14 in MeCN estimated from intensity readings published in [61] and quantum yield data of the parent compound without active PET, DMA, published in [63]. (Reprinted in part with permission from [61]. Copyright 1988 American Chemical Society)...

Figure 3 Comparison of several thionins reveals their structural similarity. The structures are color coded for their secondary structure, cyan a-helix, red /3-strand, magenta random coil/turn. (a) a-Purothionin (2plh) and (b) /3-purothionin (1 bhp) have four disulfide bonds, (c) Crambin (1 ejg) has three disulfide bonds. Despite its thionin fold it lacks antimicrobial or other toxic activity, (d) An overlay of crambin (1ejg, black), a-purothionin (2plh, red), /3-purothionin (1 bhp, orange), viscotoxin A3 (ledO, magenta), and viscotoxin B (Ijmp, cyan) from Viscum album reveals the conserved structure of the peptide backbone.

Figure 18 The image of a typical bag rendered in color and in gray scale. The color image, shown here with boosted contrast, helps guide the operator s eye to recognize objects. Organic materials are color- coded in orange, inorganic material in green, and metals in blue.

Figure 2.14 Schematic representation of the various stages of the grafting of a surface organo-tin complex on a platinum particle (as demonstrated by EXAFS, NMR, chemical analysis, IR). From left to right starting platinum particle with the surface organometallic fragment [(Pts)3(Tl -snBu]i adatoms of Sn, [(Pt4(ri -Sn]) surface PtSn alloy [sphere color-code orange (Pt), blue (H), white (C), green (Sn)].

Figure 7.4 Visualization of enrichment. Color code yellow = promoter green = exon gray= primary transcript orange = enriched region red=TSS red box = promoter prediction.

Each of the four fire divisions is indicated by a distinctive symbol (Figure 6.3) in order to be recognized by fire-fighhng personnel approaching a scene of fire. The color of all four symbols is orange in accordance witb tbe color code of UN for Class 1 (Explosives and Ammunition) and the numbers are painted in black so that these symbols can be idenhfied from a long range, the symbols differ in shape as follows. 

Fig. 7 The location on tubulin of residues that modulate the sensitivity to MT-destabilizing agents and the location of exogenous inhibitor and nucleotide sites on P tubulin. The a subunit is in semitransparent pink together with a composite P-subunit color-coded as in Fig. 3a with ball-and-stick models of bound taxol (orange), colchicine (yellow) and GDP (magenta). Ball-and-stick models of vinblastine (cyan) are drawn on the two partial vinca sites on a and on P tubulin. The sulfur atom of Cys P12 is highlighted as a yellow sphere. The sites of nine amino acid substitutions [49] that both confer resistance to vinblastine and colchicine and stabilize MTs are depicted as red (on a tubulin) or green (on P tubulin) spheres. Two residues of the P H10 helix whose mutations enhance the sensitivity to colchicine site ligands and destabilize MTs [71] are also shown as blue spheres...

Fig. 4.9 Electrostatic potential of 02N—02C—C02—N02 and oxalic acid (B3LYP/6-31G(d), 0.001 e bohr-3 isosurface, energy values -0.06 H to +0.06 H) color coding red (very negative), orange (negative), yellow (slightly negative), green (neutral), turquoise (slightly positive), light blue (positive), dark blue (very positive).

The distribution of electron density in a molecule can be shown using an electrostatic potential map. These maps are color coded to illustrate areas of high and low electron density. Electron-rich regions are indicated in red, and electron-deficient sites are indicated in blue. Regions of intermediate electron density are shown in orange, yellow, and green. 

Color Code red-tan, orange-yellow, green (mango has numerous culti-vars, or cultivated varieties, of different colors)... 

Color Code orange-yellow, red— blood pulp varieties... 

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