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The following is a list of last words attributed to various fictional characters in films.

Characters are listed according to the originating film, then the name of character the quote is attributed to in case of more than one quote per source. Where quotes come from a series of films, they are organized in the order of the films they appeared in for example, quotes from the first Kill Bill film appear before quotes from the second film, and so on.

Where possible, for the purposes of clarification, further explanatory notes have been presented.

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Additionally, if a character's final words consist of a dialogue with the other characters, the other character's speech may be included for contextual purposes; for example, if one character asks a question that the one who is about to die answers. Some characters may have more than one "death," in instances such as being resurrected, or existing temporarily as an undead being.

In some of those instances, their last words from each "death" may be added if they are significant.

Additionally, significant last words from deaths that are merely assumed to have happened or are non-canon are included.

In instances where there are multiple outcomes, or in media with alternate timelines, the character's last words will also be featured. Landing, crashing or shot down.

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But there's no way in Hell we're going back! I'm giving you a head start. He is notable for having a limited vocabulary, on which he could only say: But he actually says this phrase, which implies a bond formed between the heroes. Said out of frustration to his partner when she tells him she's found some coconuts to eat after their helicopter runs out of gasoline, leaving them stranded on a desert island. They may or may not have died, and even if they did, these may not have been Luthor's last words.

Retrieved from " https: Views Read Edit View history. This page was last edited on 13 Decemberat By using this site, you agree to the Terms of Use and Privacy Policy.

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  2. Abstract: In various embodiments, players around the casino may predict cards to be dealt in a game of blackjack. Abstract: A system for checking measurement results is provided with a urine qualitative analyzer for measuring the specific gravity of a urine, urinary particle . Inventors: Jack V. Smith, Jesse M. Carter.:
    Her (fasting) blood work showed Creatinine , BUN 51, and urine specific gravity (higher is better), all of which indicate kidney disease. . Once a week, instead of the above, give 4 oz fish (canned jack mackerel or pink salmon or sardines, drained and rinsed, approx mg) plus 2 oz tripe or. B. Anticipate a urine specific gravity to be C. Plan to administer a fluid challenge. D. Place client in Trendelenburg position. C The nurse should plan to administer a fluid challenge for hypovolemia, which is indicated by the client's low urinary output and blood pressure. A nurse is planning care for a client who has. You saw me enter the casino, did you ever see me place a bet? . Jack. Grissom: And Ecklie's at her house now. Nick: Yeah, and I can tell you what he's going to find. My fingerprints; my DNA. Grissom: What were you thinking, Nicky? .. You know, I have seen guys drink, like, five gallons of water to try and dilute their urine.
  3. Backdraft; Bad Company; Bad Taste (); The Ballad of Jack and Rose (); Barton Fink (); Batman; Battle Beyond the a congressional hearing, before she notices Lex Luthor's absence and a jar of his urine (labelled "Granny's Peach Tea" in reference to her earlier words to him).:
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Quando criamos uma identidade visual, criamos um sistema onde os elementos visuais que caracterizam o trabalho possam ser compreendidos, reconhecidos, memorizados. Diazonium ions which are useful as reagents for the assay of bilirubin content in a sample, such as a body fluid sample, are provided. In one preferred embodiment, 2-methylnitroaniline diazonium ion is provided, having the structure: STR1 Also provided are reagent compositions including the diazonium ions.

The reagent compositions may be in liquid or solid form, and further may include other components, such as buffers, carriers, and solubilizers. Salts including the diazonium ion and a counteranion also are provided. Also provided are methods of using the diazonium ions in assays to detect or quantitate bilirubin present in a sample such as a body fluid sample. Using the assays, the amount of direct, indirect, and total bilirubin in a sample may be accurately and reproducibly detected, and optionally correlated with the presence or absence of any of a variety of diseases or disorders of organs such as the liver, gall bladder or intestines.

Stable liquid urobilinogen control composition. The present invention addresses the need to ensure that clinical tests for urobilinogen in urine are properly working. The invention specifically provides a novel liquid urobilinogen composition which remains stable in liquid form for eighteen months and a method for making the same. Analysis of analytes in biological fluids.

A method for detecting an analyte in a sample uses both the specificity of an enzymatic reaction and the separation power of capillary electrophoresis. Stabilization of bilirubin in control sera and calibrators. The invention concerns a stable control serum or calibration serum containing bilirubin to analytically examine the methodical accuracy of individual parameters in human sera or patients.

The control serum or calibration serum according to the invention is used to stabilize bilirubin in solutions and to generally increase the stability of control sera or calibration sera. Geoffrey Burns, Martina Junius-Comer. Method of analyzing medical specimens with improved length of analytical run determination. In high volume laboratory analysis of patient medical specimens, control materials are inserted at periodical intervals e. If the results of the analysis deviate from the mean according to statistical rules, the run of analyses prior to the insertion of control materials has in the past been rejected, often causing a substantial loss of results because the control materials were not inserted sufficiently frequently.

According to the invention the patient mean of a test is determined, and when the mean deviates from the predetermined mean by more than a selected amount, this determination is used, not to reject the run, but rather to trigger insertion and analysis of control materials. If the analysis of control materials shows that the run is in control, the analyses made prior thereto are reported and the run is resumed.

If the control material analysis shows that the run is out of control, then the prior analyses are rejected. The present invention is directed to the assay and purification of proteins, and particularly to the non-radioactive assay and purification of protein kinases, phosphatases and protease by incubating the enzyme with a substrate modified peptide to form a product modified peptide under conditions where the enzyme is active.

The product modified peptide and substrate modified peptide are then separated, and the product modified peptide is measured. The present invention is also directed to kits and bioreagents for performing the assays. Assay method for biological components. The method is directed to assaying for biological components in a sample comprising step A generating an oxidase substrate in the presence of an amphoteric surfactant and in the absence of ferrocyanide; B initially generating hydrogen peroxide through said oxidase reaction on said substrate of oxidase with subsequent detection of the generated hydrogen peroxide using peroxidase and a color developer capable of being oxidized in the presence of amphoteric surfactant and ferrocyanide; and C correlating the amount of color developed to the amount of biological components in the biological sample.

Even when the biological component to be detected is present in a very small amount, the interference of bilirubin can be eliminated in assays of biological components in which peroxidase generated from an enzymatic reaction is detected using peroxidase and a color developer capable of being oxidized. Daiichi Pure Chemicals Co. Method for control or calibration in a chemical analytical determination. An aqueous dispersion used for control or calibration of a dry analysis element comprising at least one color producing reagent and a porous layer, which comprises water-insoluble liquid particles having a mean particle size of from about 0.

Fuji Photo Film Co. Diagnostic test system verification method using serum free glucose control containing quaternary ammnonium polymer. Disclosed is a serum free control reagent formulation useful for the determination of a pre-selected analyte.

The formulation involves an aqueous solution of a predetermined amount of the analyte together with a polymerized quaternary salt of di- or mono- allyl, di- or tri- alkyl ammonium characterized by the formulae: STR1 where R is straight or branched chain alkyl of 1 to 4 carbon atoms, n is a number of at least 9 and.

The formulation typically contains a buffer to maintain its pH at a level of about 7. A method for control or calibration in a chemical analytical determination using a dry analysis element comprising at least one color-producing reagent and a porous layer, wherein the method comprises applying an aqueous dispersion onto the porous layer and measuring the optical density of the color produced, wherein the aqueous dispersion comprises a substance which is the same as or similar to an analyte to be determined and water-insoluble particles dispersed therein, wherein the particles are particles of a homopolymer, a copolymer, phthalates, trimellitates, phosphates, benzoates, amides, phenols, aliphatic esters, hydrocarbons, halogenated hydrocarbons, adipates, sebacates and natural polymers.

Stable liquid control serum or calibration system for use in clinical diagnostics. The invention further addresses a process for the preparation of the stable liquid serum.

Thomas Wild, Peter Stegmueller. Method of bilirubin assay. In the assaying of direct and indirect bilirubin, it is has been found that organic compounds, capable of undergoing diazotization to products having absorption spectrum substantially identically to bilirubin, can be used as a calibration standard. Additionally, significant last words from deaths that are merely assumed to have happened or are non-canon are included.

In instances where there are multiple outcomes, or in media with alternate timelines, the character's last words will also be featured. Landing, crashing or shot down. But there's no way in Hell we're going back! I'm giving you a head start. He is notable for having a limited vocabulary, on which he could only say:

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Control and calibration solutions are described that provide control and calibration data that is recognized by a test meter allowing the meter to segregate the control and calibration data from regular test data.

Recognition and segregation of the control and calibration data can occur automatically with no additional input from the meter's user. Methods for use of the solutions are also provided. Device and kit for calibrating bodily fluid sampling devices. Method and system for checking measurement result.

A system for checking measurement results is provided with a urine qualitative analyzer for measuring the specific gravity of a urine, urinary particle analyzer for measuring urine conductivity, and a computer. The urine specific gravity measured by the urine qualitative analyzer, and the urine conductivity measured by the urinary particle analyzer are respectively transmitted to the computer.

The correlative relationship between urine specific gravity and urine conductivity is stored in the memory of the computer, and the computer determines whether or not the received urine specific gravity and conductivity match the correlative relationship, and this determination result is output. Quality control material for reagentless measurement of analytes. A method of monitoring calibration of a spectrophotometric apparatus that includes one or more than one calibration algorithm for one or more than one analyte, involves measuring absorbance of a quality control material with the apparatus to obtain a measurement, calculating one or more than one value from the measurement using the one or more than one calibration algorithm, and comparing the one or more than one value with an assigned value given to the quality control material for each of the one or more than one analyte.

The quality control material exhibits an absorbance spectrum having a negative slope for a continuous spectral segment from about 5 nm to about nm in length, and the spectral segment includes a principal calibration wavelength for the one or more than one analyte. A reagentless method for determining the concentration of one or more than one analyte in a sample in a spectrophotometric apparatus having at least one primary calibration algorithm is also disclosed.

A method of monitoring calibration of a spectrophotometric apparatus having one or more than one calibration algorithm for one or more than one analyte. This method involves measuring an absorbance of a quality control material to obtain a measurement, calculating one or more than one concentration value from the measurement using the one or more than one calibration algorithm, and comparing the one or more than one concentration value with an assigned value given to the quality control material for each of the one or more than one analyte.

The quality control material exhibits an absorbance spectra having a negative slope for a continuous spectral segment from about 5 nm to about nm in length, or a wavelength therebetween. A reagentless method for determining the concentration of one or more than one analyte in a sample in a spectrophotometric apparatus containing one or more than one primary calibration algorithm is also provided.

The present invention provides a method of monitoring calibration of a spectrophotometric apparatus that comprises one or more calibration algorithms for one or more analytes.

This method comprises measuring absorbance of a quality control material with the apparatus to obtain a measurement, where the quality control material exhibits an absorbance spectra characterized as having a negative slope for a continuous spectral segment from about 5 nm to about nm in length, and where the spectral segment includes a principal calibration wavelength for the one or more analytes.

The method then involves calculating on or more concentration values from the measurement using the one or more calibration algorithms, followed by comparing the one or more concentration values with an assigned value given to the quality control material for each of the one or more analytes, and determining if there is a violation of a pre-established quality control rule. Non-oxidizable bilirubin substitutes and uses therefor.

Compositions and methods are disclosed for use in the analysis and quantitation of conjugated and unconjugated bilirubin in patient or other samples. The compositions have the general formula: R1 and R2 are independently selected from alkyl and aryl, R3 and R4 are independently selected from hydrogen, alkyl, alkenyl, tauryl, aryl, and glucoronyl, and R5, R6, R7, R8, R9 and R10 are each independently selected from hydrogen and alkyl, and are resistant to oxidation, as occurs in bilirubin upon exposure to light and air.

These properties make them ideal for use in calibration and control solutions for use in medical and research bilirubin analysis, or other applications where stable reagents for bilirubin analysis is desirable.

Medical Analysis Systems, Inc. The invention provides a cDNA which encodes tapasin-like protein. It also provides for the use of the cDNA, protein, and antibody in the diagnosis, prognosis, treatment and evaluation of therapies for cancer.

The invention further provides vectors and host cells for the production of the protein and transgenic model systems. Micromachined fluid analysis device and method. The device is a micromachined filtering device comprising a substrate with through-thickness vias having approximately equal diameters that prevent passage through the substrate of a first material while permitting passage through the substrate of other materials having diametrical dimensions less than the diameter of the vias.

Electrodes are located on a surface of the substrate between vias so that as the first material collects at the surface of the substrate, the electrodes become electrically connected to produce an output signal in some proportion to the amount of the first material collected.

The device can incorporate multiple micromachined substrates, yielding an analysis system that produces an electrical output for each of a number of properties or parameters. Use of bathocuproine for the evaluation of the antioxidant power in liquids and solutions. The antioxidant power of an organic or inorganic liquid is determined by causing it to enter into competition with bathocuproine BC in a copper sulphate solution.

Bathocuproine BC forms stable complexes with the monovalent Cu. Cu II in solution can be reduced to Cu I by a number of reducing compositions belonging to a class of compositions consisting prevailingly of both liposoluble and water soluble non-enzymatic antioxidants. When the reaction occurs in a bathocuproine BC buffer, the complex being formed is characterized by the concentration of the reducing agents and then, by good approximation, of the antioxidants present in the system.

The quantitative analysis of such a reaction can be easily made by spectrophotometry at nm both by macro- and micromethods with the use of a number of reducing standard compositions with known concentrations. Margit Doth, Christoph Petry.

Calibrator material for instruments which measure interferents in serum and plasma specimens. A quality control material is disclosed which is used to monitor the calibration or used for recalibration of instruments used to screen for interferents in serum or plasma specimens. In particular, the quality control material disclosed is used to monitor instrument calibrations or used for recalibration for instruments which assess the amount of hemolysis, turbidity, bilirubinemia and biliverdinemia, either separately, or any two, or any three, or all four simultaneously, in plasma or serum samples.

The quality control material does not contain any blood products such as plasma lipids, bile pigments, or hemoglobin, is stable at room temperature, and is ready for use with up to four constituents.

Method of detection of bilirubin in urine on an automated analyzer. Method for detecting total bilirubin in urine using a chemical detection means with an indicator that will produce a detectable quantitative response in the presence of bilirubin in urine on an automated analyzer.

Measurement of bilirubin albumin binding. The present invention is directed to the determination of unconjugated and unbound bilirubin in a sample. Research Corporation Technologies, Inc. Diazonium ion assay reagents and methods for their use. Diazonium ions which are useful as reagents for the assay of bilirubin content in a sample, such as a body fluid sample, are provided. In one preferred embodiment, 2-methylnitroaniline diazonium ion is provided, having the structure: STR1 Also provided are reagent compositions including the diazonium ions.

The reagent compositions may be in liquid or solid form, and further may include other components, such as buffers, carriers, and solubilizers. Salts including the diazonium ion and a counteranion also are provided.

Also provided are methods of using the diazonium ions in assays to detect or quantitate bilirubin present in a sample such as a body fluid sample. Using the assays, the amount of direct, indirect, and total bilirubin in a sample may be accurately and reproducibly detected, and optionally correlated with the presence or absence of any of a variety of diseases or disorders of organs such as the liver, gall bladder or intestines.

Stable liquid urobilinogen control composition. The present invention addresses the need to ensure that clinical tests for urobilinogen in urine are properly working.

The invention specifically provides a novel liquid urobilinogen composition which remains stable in liquid form for eighteen months and a method for making the same. Analysis of analytes in biological fluids. A method for detecting an analyte in a sample uses both the specificity of an enzymatic reaction and the separation power of capillary electrophoresis.

Stabilization of bilirubin in control sera and calibrators. The invention concerns a stable control serum or calibration serum containing bilirubin to analytically examine the methodical accuracy of individual parameters in human sera or patients. The control serum or calibration serum according to the invention is used to stabilize bilirubin in solutions and to generally increase the stability of control sera or calibration sera. Geoffrey Burns, Martina Junius-Comer.

Additionally, significant last words from deaths that are merely assumed to have happened or are non-canon are included. In instances where there are multiple outcomes, or in media with alternate timelines, the character's last words will also be featured. Landing, crashing or shot down.

But there's no way in Hell we're going back! I'm giving you a head start. He is notable for having a limited vocabulary, on which he could only say: But he actually says this phrase, which implies a bond formed between the heroes. Said out of frustration to his partner when she tells him she's found some coconuts to eat after their helicopter runs out of gasoline, leaving them stranded on a desert island. They may or may not have died, and even if they did, these may not have been Luthor's last words.

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Achei o projeto genial! AntiCast Expresso 7 AntiCast. Baseadas em imagens de suas terras natais. O texto do Dado resume essa ideia. Mas seu texto dani, como sempre, excelente. Some characters may have more than one "death," in instances such as being resurrected, or existing temporarily as an undead being. In some of those instances, their last words from each "death" may be added if they are significant. Additionally, significant last words from deaths that are merely assumed to have happened or are non-canon are included.

In instances where there are multiple outcomes, or in media with alternate timelines, the character's last words will also be featured. Landing, crashing or shot down. But there's no way in Hell we're going back! I'm giving you a head start. He is notable for having a limited vocabulary, on which he could only say: But he actually says this phrase, which implies a bond formed between the heroes. Said out of frustration to his partner when she tells him she's found some coconuts to eat after their helicopter runs out of gasoline, leaving them stranded on a desert island.

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