Abstract: The present invention is related to a process for the preparation of zeolitic material through condensed gel crystallizations and their use in an FCC Catalyst composition. The present disclosure describes methods for improved preparation of zeolites by preparing an aqueous precursor mixture; removing at least 5 wt % of the total water from the aqueous precursor solution to create a solution with greater solids content; crystallizing the solution of step (b) to create a zeolite product. The resulting zeolite is used in an FCC catalyst composition comprising about 2 to about 80 wt % one or more zeolite, about 15 to about 50 wt % quasicrystalline boehmite, about 0 to about 50 wt % microcrystalline boehmite, and greater than about 0 to about 25 wt % silica.

Abstract: The present invention is related to a process for the preparation of zeolitic material through condensed gel crystallizations and their use in an FCC Catalyst Additive composition. The present disclosure describes methods for improved preparation of zeolites by preparing an aqueous precursor mixture; removing at least 5 wt % of the total water from the aqueous precursor solution to create a solution with greater solids content; crystallizing the solution of step (b) to create a zeolite product. The resulting zeolite is used in an FCC Catalyst Additive composition comprising about 10 to about 70% wt % one or more zeolites, 0 wt % to about 25 wt % silica; 0 to about 50 wt % added alumina; and 0 to about 20% P2O5.

Abstract: A secondary growth procedure described herein is used to prepare finned zeolites. The finned zeolites possess properties that are distinctly unique compared to crystals of similar size lacking fins. The procedure is amenable to a wide range of zeolite crystal structures.

Abstract: The present invention provides a multiplex ligation-dependent probe microarray detection. Specifically, a surface probe-based quantitative PCR detection system in the present invention comprises: (a) a solid phase carrier; (b) a first probe; (c) a second probe; (d) a ligase for ligating the first probe and the second probe to form a third probe; (e) a quenching primer pair for amplifying the third probe; and (f) a quenching product capture nucleic acid immobilized on the solid phase carrier and matching a quenching amplification product. The present invention further provides a corresponding detection method and detection apparatus, and applications thereof. The present invention can rapidly, easily, efficiently, and simultaneously perform quantitative detection on multiple target sequences.

Abstract: Canine CCK1 receptor materials are described, such as polypeptides having amino acid sequences corresponding to SEQ ID Nos.: 14, 15, and 16 or functional variants thereof and polynucleotides expressing them having nucleic acid sequences corresponding to SEQ ID Nos.: 11, 12, and 13 or complements thereof. Such materials are useful as reagents in drug screening assays to identify compounds having CCK1R-modulating activity.

Abstract: The present invention relates to methods and systems for database comparison and database searching and matching, and specifically to database comparison and database searching and matching of databases containing biomolecular sequences as well as databases comprising matched sequences, as well as the use of databases comprising matched biomolecular sequences. In addition, a database comprising matched sequences or a database comprising matched biomolecular sequences may be accessed via a graphical user interface.