Method of marking a hydrocarbon liquid includes adding to the liquid, a tracer compound of Formula I or II:

##STR00001##

wherein at least one of R.sup.1-R.sup.6 in Formula I and at least one of R.sup.7-R.sup.14 in Formula II is selected from: i. a bromine or fluorine atom; ii. a partially or fully halogenated alkyl group; iii. a branched or cyclic C.sub.4-C.sub.20 alkyl group; iv. an aliphatic substituent linking two positions selected from R.sup.1- R.sup.6 in Formula I to one another or two positions selected from R.sup.7-R.sup.14 in Formula II to one another; or v. a phenyl group substituted with a halogen atom, an aliphatic group or halogenated aliphatic group and none of R.sup.1-R.sup.6 and none of R.sup.7-R.sup.14 being a sulphonate group or COOR.sup.15, where R.sup.15 represents H, C.sub.1-C.sub.20 alkyl, C.sub.2-C.sub.20 alkenyl, C.sub.2-C.sub.20 alkynyl, C.sub.3-C.sub.15 cycloalkyl or aryl.

Polymer microparticles spatially and spectrally encoded using upconversion nanocrystals (UCN) are described for labeling of articles and tissues. UCN having spectrally distinguishable emission spectra are disposed in different portions of an encoding region of each microparticle.

A method of marking a hydrocarbon liquid includes the step of adding to the liquid, as a tracer compound, a compound of Formula I:

##STR00001##

wherein at least one of R.sup.1-R.sup.4 is selected from: i. a bromine or fluorine atom; ii. a partially or fully halogenated alkyl group; iii. a branched or cyclic C.sub.4-C.sub.20 alkyl group; iv. an aliphatic substituent linking two positions selected from R.sup.1-R.sup.4 in Formula I to one another; or v. a phenyl group substituted with a halogen atom, an aliphatic group or halogenated aliphatic group. The tracer compounds are resistant to removal from the fuel by chemical laundering or by contact with absorbents such as charcoal.

Method of marking a hydrocarbon liquid includes adding to the liquid, a tracer compound of Formula I or II: ##STR00001##
wherein at least one of R.sup.1-R.sup.6 in Formula I and at least one of R.sup.7-R.sup.14 in Formula II is selected from: i. a bromine or fluorine atom; ii. a partially or fully halogenated alkyl group; iii. a branched or cyclic C.sub.4-C.sub.20 alkyl group; iv. an aliphatic substituent linking two positions selected from R.sup.1-R.sup.6 in Formula I to one another or two positions selected from R.sup.7-R.sup.14 in Formula II to one another; or v. a phenyl group substituted with a halogen atom, an aliphatic group or halogenated aliphatic group and none of R.sup.1-R.sup.6 and none of R.sup.7-R.sup.14 being a sulphonate group or COOR.sup.15, where R.sup.15 represents H, C.sub.1-C.sub.20 alkyl, C.sub.2-C.sub.20 alkenyl, C.sub.2-C.sub.20 alkynyl, C.sub.3-C.sub.15 cycloalkyl or aryl.

A method of identifying a product comprises forming a tagged product by adding to said product a tracer material comprising at least one tracer compound which is acceptable for use as an additive in food and subsequently analyzing a sample of said product to determine the presence of said tracer compound thereby to determine whether said sample is a sample of the tagged product. The method is especially useful for the identification of vegetable oil products from sustainably managed sources. The use of permitted food additives as tracers enables the product to be identified in the supply chain while also allowing it to be used safely in foodstuffs if required.

The present invention provides a method for the analysis of a compound with amino group (e.g., an amino acid or peptide) contained in a sample and convenient manner with a high sensitivity. The compound with amino group in a sample containing the compound with amino group is labeled with a specific carbamate compound such as p-trimethylammonium anilyl-N-hydroxysuccinimidyl carbamate iodide to enhance the selectivity and sensitivity. The present invention is preferably used in conjunction with mass spectrometry such as MS/MS method to facilitate quantitative analysis. The present invention further provides labeling reagents for mass spectrometry.

A titration method uses a tracer in the titrant or titrand to quantify the amount of titrant added. The method does not require quantitative addition of titrant or sample. The tracer can be inert or can participate as an indicator of the titrant-analyte reaction. The tracer concentration is quantified by an appropriate method depending upon the type of tracer and analytical performance desired (e.g. precision, accuracy). The method simplifies titrations because it eliminates the need for a precision dispensing device and analytical balance.

Described herein are particular embodiments relating to a microfluidic device that may be utilized for cell sensing, counting, and/or sorting. Particular aspects relate to a microfabricated device that is capable of differentiating single cell types from dense cell populations. One particular embodiment relates a device and methods of using the same for sensing, counting, and/or sorting leukocytes from whole, undiluted blood samples.

Methods and compositions are provided that include a multichromophore and/or multichromophore complex for identifying a target biomolecule. A sensor biomolecule, for example, an antibody can be covalently linked to the multichromophore. Additionally, a signaling chromophore can be covalently linked to the multichromophore. The arrangement is such that the signaling chromophore is capable of receiving energy from the multichromophore upon excitation of the multichromophore. Since the sensor biomolecule is capable of interacting with the target biomolecule, the multichromophore and/or multichromophore complex can provide enhanced detection signals for a target biomolecule.

A method of marking a hydrocarbon liquid includes the step of ##STR00001##
adding to the liquid, as a tracer compound, a compound of Formula I:
wherein at least one of R.sup.1-R.sup.4 is selected from: i. a bromine or fluorine atom; ii. a partially or fully halogenated alkyl group; iii. a branched or cyclic C.sub.4-C.sub.20 alkyl group; iv. an aliphatic substituent linking two positions selected from R.sup.1-R.sup.4 in Formula I to one another; or v. a phenyl group substituted with a halogen atom, an aliphatic group or halogenated aliphatic group. The tracer compounds are resistant to removal from the fuel by chemical laundering or by contact with absorbents such as charcoal.