Dunn et al., “Mapping Viral, RNA by Sandwich Hybridization” Methods in Enzymology, vol. 65, pt. 1, 1980, pp. 468-479.* |
L. J. Emorine et al., “Structure of the gene for human β2-adrenergic receptor: Expression and promoter characterization”, Proceedings of the National Academy of Science, USA, vol. 84, Oct. 1987, pp. 6995-6999. |
C. B. Harley, “Hybridization of Oligo(dT) to RNA on Nitrocellulose”, Gene Analysis Techniques, vol. 4, 1987. pp. 17-22. |
A. Palva et al., “Laboratory Methods: Quantification of α-Amylase mRNA in Bacillus subtilis by Nucleic Acid Sandwich Hybridization”, DNA, vol. 7, No. 2, 1988, pp. 135-142. |
R. Nussinov, “Efficient algorithms for searching for exact repetition of nucleotid sequences.”, Journal of Molecular Evolution, vol. 19, Nos. 3-4, pp. 283-285. |
W. W. Ralph et al., “A modified Chou and Fasman protein structure algorithm,”, Computer Application in the Biosciences, vol. 8, No. 3, Sep. 1987, pp. 211-216. |
C. Hough et al., “Differential down-regulation of β1-and β2-adrenergic receptor mRNA in C6 glioma cells”, Biochemical and Biophysical Research Communications, vol. 170, No. 1, 1990, pp. 46-52. |
A. Ballagi-Pordany et al., “Quantitive determination of mRNA phenotypes by the polymerase chain reation”, Analytical Biochemistry, vol. 196, 1991, pp. 89-94. |
B. Feve et al., “Differential regulation of β1-and β2-adrenergic receptor protein and mRNA levels by glucocorticoids during 3T3-F442A adipose differentiation”, Journal of Biological Chemistry, vol. 265, No. 27, Sep. 25, 1990, pp. 16343-16349. |
P. Muzzin et al., “An adipose tissue-specific β-adrenergic receptor”, Journal of Biological Chemistry, vol. 266, No. 35, Dec. 15, 1991, pp. 24053-24058. |
C. Albretsen et al., “Optimal conditions for hybridization with oligonucleotides: a study with myc-oncogene DNA probes”, Analytical Biochemistry, vol. 170, 1988, pp. 193-202. |
M. S. Waterman et al., “Phase transitions in sequence matches and nucleic acid structure”, Proceedings of the National Academy of Science USA, vol. 84, Mar. 1987, pp. 1239-1243. |
M. S. Waterman et al., “A new algorithm for best subsequence alignments with application to tRNA-rRNA comparisons”, Journal of Molecular Biology, vol. 197, 1987, pp. 723-728. |
R. J. Cano et al., “DNA hybridization assay using ATTOPHOS™, a fluorescent substrate for alkaline phosphatase”, Biotechniques, vol. 12, No. 2, Feb. 1992, pp. 264-269. |
N. P. Gerard, “Human substance P receptor (NK-1):Organization of the gene, chromosome localization, and functional expression of cDNA clones”, Biochemistry, vol. 30, 1991, pp. 10640-10646. |
S. -I. Hirai et al., “Characterization of junD: a new member of the jun protooncogene family”, The EMBO Journal, vol. 8, No. 5, 1989, pp. 1433-1439. |
D. T. Jones et al., “Molecular cloning of five GTP-binding protein cDNA species from rat olfactory neuroepithelium”, Journal of Biological Chemistry, vol. 262, No. 29, Oct. 15, 1987, pp. 14241-14249. |
L. Li et al., “Different members of the jun protooncogene family exhibit distinct patterns of expression in response to type β transforming growth factor”, Journal of Biological Chemistry, vol. 265, No. 3, Jan. 25, 1990, pp. 1556-1562. |
Y. Yokota et al., “Molecular characterization of a functional cDNA for rat substance P receptor”, Journal of Biological Chemistry, vol. 264, No. 30, Oct. 25, 1989, pp. 17649-17652. |
J. Codina et al., “αi-3 cDNA encodes the α subunit of Gk, the stimulatory G protein of receptor-regulated K+ channels”, Journal of Biological Chemistry, vol. 263, No. 14, May 15, 1988, pp. 6746-6750. |
H. Itoh et al., “Presence of three distinct molecular species of Gi protein α subunit”, Journal of Biological Chemistry, vol. 263, No. 14, May 15, 1988, pp. 6656-6664. |
K. Hattori et al., “Structure and chromosomal localization of the functional intronless human JUN protooncogene”, Proceedings of the National Academy of Science USA, vol. 85, Dec. 1988, pp. 9148-9152. |
P. Bray et al., “Human cDNA clones for an α subunit of Gi signal-transduction proteins”, Proceedings of the National Academy of Science USA, vol. 84, Aug. 1987, pp. 5115-5119. |
C. R. Beals et al., “A small multigene family encodes Gi signal-transduction proteins”, Proceedings of the National Academy of Science USA, vol. 84, Nov. 1987, pp. 7886-7890. |
B. A. Harris, “Complete cDNA sequence of a human stimulatory GTP-binding protein alpha subunit”, Nucleic Acids Research, vol. 16, No. 8, 1988, p. 3585. |
R. Mattera et al., “Identification by molecular cloning of two Forms of the α-subunit of the human liver stimulatory (Gs) regulatory component of adenylyl cyclase”, FEBS Letters, vol. 206, No. 1, Sep. 1986, pp. 36-42. |
J. R. Didsbury et al., “Molecular cloning of a new human G protein”, FEBS Letters, vol. 219, No. 1, Jul. 1987, pp. 259-263. |
A. Swaroop et al., “Differential expression of novel Gsα signal transduction protein cDNA species”, Nucleic Acids Research, vol. 19, No. 17, 1991, pp. 4725-4729. |
Polsky-Cynkin et al., “Use of DNA Immobilized on Plastic and Agarose Supports to Detect DNA by Sandwich Hybridization”, Clinical Chemsitry, vol. 31, No. 9, 1985, pp. 1438-1443. |
Kitabayashi et al., “Nucleotide Sequence of Rat c-jun Protooncogene”, Nucleic Acids Research, vol. 18, No. 11, 1990, EMBL Accession No. X17215. |
Hershey et al., “Molecular Characterization of a Functional cDNA Encoding the Rat Substance P Receptor”, Science, vol. 247, Feb. 23, 1990, pp. 958-961. |
Chung et al., “Cloning and Sequence Analysis of the Human Brain B-adrenergic Receptor”, FEBS Letters, vol. 211, No. 2, pp. 200-206. |
Saiki et al., “Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase”, Science, vol. 239, Jan. 29, 1988, pp. 487-491. |
I. Raineri et al., “Improved Efficiency for Single-Sided PCR by Creating a Reusable Pool of First-Strand cDNA Coupled to a Solid Phase”, Nucleic Acids Research, vol. 19, No. 14, 1991, p. 4010. |
S. Inouye et al., “Microplate Hybridization of Amplified Viral DNA Segment”, Journal of Clinical Microbiology, vol. 28, No. 6, Jun. 1990, pp. 1469-1472. |
R. Bischoff et al., “Introduction of 5'-Terminal Functional Groups into Synthetic Oligonucletides for Selective Immobilization”, Analytical Biochemistry, vol. 164, No. 2, Aug. 1, 1987, pp. 336-344. |
J. Rey-Campos et al., “Synthesis of Thymosin α1 Precursor cDNA and Purification of Active mRNA by Affinity Chromatography”, International Journal of Biochemistry, vol. 15, 1983, pp. 155-157. |
T. Atkinson et al., “A convenient procedure for the synthesis of oligodeoxyribonucleotide affinity columns for the isolation of mRNA”, Nucleic Acids Research, vol. 16, No. 13, 1988, p. 6232. |
J. A. Arias et al., “Promoter-dependent Transcription by RNA Polymerase II Using Immobilized Enzyme Complexes”, Journal of Biological Chemistry, vol. 264, No. 6, 1989, pp. 3223-3229. |
Y. Masu et al., “cDNA cloning of bovine substance-K receptor through oocyte expression system”, Nature, vol. 329, No. 29, 1987, pp. 836-838. |
C. R. Thrash et al., “Synthesis of RNA from Cellulose-bound Complementary DNA”, Journal of Biological Chemistry, vol. 252, No. 16, 1977, pp. 5615-5618. |
S. L. Griffiths et al., “Diabetes-induced changes in guanine-nucleotide-regulatory-protein mRNA detected using synthetic oligonucleotide probes”, European Journal of Biochemistry, vol. 193, No. 2, 1990, pp. 367-374. |
Y. Wataya et al., “Kagaku Ryoho no Ryoiki”, vol. 8, No. 3, 1992, pp. 487-496. |
M. S. Urdea et al., “A comparison of non-radiosotopic hybridization assay methods using fluoroscent chemiluminescent and enzyme labeled synthetic oligodeoxyribonucleotide probes”, Nucleic Acids Research, vol. 16, No. 11, 1988, pp. 4937-1956. |
Bethesda Research Laboratories Life Technologies, Inc. Product: Vanadyl Ribonucleoxide Complex. |
Biofeedback; “A Procedure for Productive Coupling of Synthetic Oligonucleotides to Polystyrene Microtier Wells for Hybridization Capture”; Biotechniques; vol. 8, p. 278-279, 1990. |
Pal Venetianer, et al., Pro Nat. Acad. Sci. USA, Vl. 71, No. 10,pp. 3892-3895, Oct. 1974; “Enzymatic Synthesis of Solid Phase-Bound DNA Sequences Corresponding to Specific Mammalian Gene”. |
P.T. Gilham, Journal of the American Chemical Society, vol. 86, pp. 4982-4985; “The Synthesis of Polynucleotide-Celluloses and Their use in the Fractionation of Polynucleotides”. |
M.R. Ven Murthy, et al., Nucleic Acids Research, vol. 14, No. 17, Jul. 24, 1986; “Preparation and Biochemical Manipulation of mRNAs and CDNAs on small Oligo(dt)-cellulose discs”. |
Jane A. Matthews, et al., Analytical Biochemistry 169, pp. 1-25 (1988); “Analytical Strategies for the Use of DNA Probes”. |
Stefan Stamm, et al., Nucleic Acids Research, vol. 19, No. 16, pp. 1350; “Sanchored PCR: PCR with cDNA Coupled to a Solid Phase”. |
R. Julian S. Duncan, et al., Analytical Biochemistry 132, pp. 68-73 (1983); “A New Regent Which May Be Used to Introduce Sulfhydryl Groups into Proteins, and Its Us in the Preparation Conjugates for Immunoassay”. |
Seiichi Hashida, et al., Journal of Applied Biochemistry 6, pp. 56-63 (1984) ; “More Useful Maleimide Compounds for the Conjugation of Fab' to Horseradish Peroxidase through Thiol Groups in the Hinge”. |
Hidenori Yamada, et al., Biochemistry 1981, 20 pp. 4836-4842; “Selective Modification of Aspartic Acid-101 in Lysozyme by Carbodiimide Reaction”. |
James V. Staros, et al., Analytical Biochemistry 156, pp. 220-222(1986); “Enhancement by N-Hydroxsuccinimide of Water-Soluble Carbodiimide-Mediated Coupling reactions”. |
Norman Arnheim, et al., C&EN, Oct. 1, 1990, pp. 36-46; “Polymerase Chain Reaction”. |