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31 results about "ALDH2" patented technology

Aldehyde dehydrogenase, mitochondrial is an enzyme that in humans is encoded by the ALDH2 gene located on chromosome 12. This protein belongs to the aldehyde dehydrogenase family of enzymes. Aldehyde dehydrogenase is the second enzyme of the major oxidative pathway of alcohol metabolism. Two major liver isoforms of aldehyde dehydrogenase, cytosolic and mitochondrial, can be distinguished by their electrophoretic mobilities, kinetic properties, and subcellular localizations.

4-Methylpyrazole Formulations for Inhibiting Ethanol Intolerance

InactiveUS20080021083A1Avoid symptomsReducing ALDH activityOrganic active ingredientsBiocideMedicineAcetaldehyde
Methods, articles of manufacture and compositions are provided useful for the prevention or amelioration of a symptom of acetaldehyde accumulation or ethanol intolerance in a subject with reduced or absent reduced or absent aldehyde dehydrogenase subtype 2 (ALDH2) activity wherein about 1 mg / kg to about 4 mg / kg 4-methylpyrazole, or an equivalent mass of a 4-MP salt, are to be orally administered to the subject.
Owner:RAPTOR PHARMA

Method and set for detecting alcohol metabolizing genes

The present invention relates to a method and a set for detecting alcohol metabolizing genes. The present invention provides a method and a reagent for detecting alcohol dehydrogenase (ADH1B) and aldehyde dehydrogenase (ALDH2). The method and the reagent have enough specifity and sensitivity, can save complicated steps for learning the technology, and can save time and manpower. The present invention further provides a method and a set for detecting an individual who has a high cancer risk after consuming alcohol.
Owner:CHI MEI MEDICAL CENT

Primer for detecting alcohol metabolizing genes by aid of pyrosequencing joint sequencing methods and application of primer

The invention discloses a primer for detecting alcohol metabolizing genes by the aid of pyrosequencing joint sequencing methods, and belongs to the technical field of biological detection. The primer comprises amplification primers shown as SEQ ID NO.1-4 and sequencing primers shown as SEQ ID NO.5-6. Biotin labeling is carried out by 5' ends of the primers shown as SEQ ID NO.1 and SEQ ID NO.3. The invention further discloses application of the primer to simultaneously detecting the polymorphism of SNP (single nucleotide polymorphism) loci rs671 of ALDH2 (acetaldehyde dehydrogenase 2) genes and SNP loci rs1229984 of ADH1B (alcohol dehydrogenase 1B) genes. The primer is high in detection throughput as compared with the traditional ordinary pyrosequencing with only single-SNP polymorphism detection capacity during sequencing reaction in each procedure, the detection time can be effectively shortened, and labor and the cost can be effectively reduced. Besides, the primer and the application have the advantages of accurate detection results, good specificity, high sensitivity, short detection cycle, simplicity in operation and capability of meeting clinical examination requirements.
Owner:石家庄迪安医学检验实验室有限公司

Positive reference taking GG type of 1510 site of human ALDH2*2 gene as template

InactiveCN107326087ASolve quality inspection problemsVerify accuracyMicrobiological testing/measurementALDH2Cancer research
The invention relates to a positive reference taking a GG type of a 1510 site of a human ALDH2*2 gene as a template. The positive reference is characterized in that the positive reference is a reagent mainly comprising a base sequence. The base sequence comprises a human ALDH2*D gene fragment which is as shown in SEQ NO:4, wherein the base site with an underline is the 1510 site of the human ALDH2*D gene, and the 1510 site is used for representing a position wherein the GG type of the human ALDH2*D gene can be mutated to an AA type of the human ALDH2*D gene. The positive reference provided by the invention is used for verifying whether the detection result that a detected sample whether contains the GG type of the 1510 site of the human ALDH2*D gene or not is correct or not, and solves the quality detection problem of the human ALDH2*D gene.
Owner:TOYO TOYOBO CO LTD

Reagent kit for detecting children disease genetic susceptibility

The present invention provides a kit of detecting genetic predisposition of children syndrome. The kit includes specific primer pairs and specific fluorescent probe pairs for detecting 28 SNP polymorphism genotypes on the genes NOS3, CTLA4, ENOS, ERCC1, ERCC2, MTHFR, MTRR, MTR, MS4A2, XRCC1, ALDH2, TNFA, CCL5, PARP1, OPG, VDR, PON1, AGT, CCND1, UCP2, ADH2, ADBR2, APOB, CYP11B2, CYP1A1, CYP2E1, CETP, NQO1 at the same time, and normal components for FQ-PCR detection. The kit of the invention evaluates the genetic predisposition of children syndrome by detecting the genotypes of the 28 SNP polymorphism sites at the same time which is tightly relative to the genetic predisposition of children syndrome.
Owner:XINBAXIANG SHANGHAI MOLECULAR MEDICAL TECH SHANGHAI

Molecule associated with onset of gout, and method and kit for evaluating diathesis of uric acid-related diseases and inflammation-related diseases, and inspection object and drug

InactiveUS20170002413A1Reduce expenditureLoss and decrease in functionNervous disorderPeptide/protein ingredientsDiseaseMedicine
To specify a molecule associated with the onset of gout so as to provide a method for evaluating a diathesis of uric acid-related diseases and a diathesis of inflammation-related diseases, an evaluation kit for carrying out the method, an inspection object, and a drug, on the basis of the molecule specified above, for contributing to the early treatment and prevention of the uric acid-related diseases and inflammation-related diseases. The molecule includes any one protein and cDNA of CNIH2-PACS1, ALDH2, MYL2-CUX2, GCKR, MAP3K11, NPT4, ABCG2, HIST1H2BF / HIST1H4E, HIST1H2BE / HIST1H4D and FAM35A, or proteins of combination thereof with GLUT9, NPT1, URAT1, or NXRN2, and is capable of selectively inducing gout. A molecule includes protein and cDNA of an ABCG2 variant and is capable of selectively and ATP-dependently decreasing urate excretion.
Owner:THE UNIV OF TOKYO

Methods and compositions for treating diseases

ActiveUS20160310579A1Reduces and eliminates toxicityOrganic active ingredientsPeptide/protein ingredientsALDH2Toxicity
The present invention provides methods and compositions comprising ALDH2 in the treatment of a patient with toxicity resulting from ALDH2 deficiency. The physiological states that may be treated using the present invention include temporary ALDH2 deficiency, such as that seen by alcohol poisoning or an ischemic event.
Owner:KATSNELSON ILANA

Nitroglycerin metabolism marker detection kit and detection method and application thereof

The invention discloses a nitroglycerin metabolism marker detection kit and a detection method and application thereof. The detection kit is used for detecting the gene polymorphism of a nitroglycerin metabolism marker gene locus ALDH2G1510A, and the kit comprises an ALDH2G1510A amplification primer, an ALDH2G1510A sequencing primer and a positive control. According to the method, ALDH2 (G1510A) is amplified through RPA, a large number of amplification products are rapidly and effectively generated at the constant temperature, single-stranded DNA is specifically captured through an amino-labeled single-stranded DNA analogue directly combined with carboxyl modifier, after washing, a sequencing primer and template DNA are added for annealing, and a sequencing raw material is added for pyrosequencing.
Owner:湖南菲思特精准医疗科技有限公司

A genetic detection kit for alcohol assessment

The invention provides a gene detection reagent kit for evaluating alcohol tolerance. The gene detection reagent kit comprises six amplification primers for three genes including an internal reference gene GAPDH (glyceraldehyde phosphate dehydrogenase), a gene ADH1B (ethanol dehydrogenase 1B) and a gene ALDH2 (acetaldehyde dehydrogenase 2) and five Taq-man probe primers. One of the Taq-man probe primers is positioned at the internal reference gene GAPDH and is used for carrying out FAM fluorescence labeling; two other Taq-man probe primers are SNP (single nucleotide polymorphism) probes positioned at the gene ADH1B and are used for carrying out VIC and ROX (roxithromycin) labeling; the remaining two Taq-man probe primers are SNP probes positioned at the gene ALDH2 and are used for Cy5 and Quasar705 labeling, BHQ is used as a quenching group, and delta ct values can be computed. The gene detection reagent kit has the advantages that the alcohol tolerance of healthy persons can be evaluated by the gene detection reagent kit from the aspect of genes, and accordingly the healthy persons can know the strength and the weakness of alcohol tolerance, can drink alcohol scientifically and can carry on occasion such as party, gathering and banquet related to alcohol culture.
Owner:TIANJIN KANGTING BIOLOGICAL ENG GRP CO LTD
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