1. Substrate for polymerase activity determination

2. An RNA polymerase inhibitorAcridine Orange

3. This invention discloses high-affinity oligonucleotide ligands to the thermostable $i(Taq) polymerase and $i(Tth) polymerase.

4. Cresol Red does not inhibit Taq polymerase

5. Cresol Red does not inhibit Taq polymerase

6. Bst DNA Polymerase, Large Fragment is the portion of the Bacillus stearothermophilus DNA Polymerase protein that contains the 5´ → 3´ polymerase activity, but lacks 5´ →3´ exonuclease activity

7. Method for testing mutant gene through real-time polymerase chain reaction using dna polymerase with inhibited activity of 5'-flap endonuclease

8. THERMOSTABLE $i(IN VITRO) COMPLEX WITH POLYMERASE ACTIVITY

9. Azt triphosphate also inhibits the DNA polymerase of HBV

10. Pre-Aliquoted PCR master mix can be ordered with ThermoPrime Taq DNA Polymerase, Extensor Hi-Fidelity PCR Enzyme Mix or Thermo-Start Taq DNA Polymerase.

11. Basidiomycota, elongation factor 1-alpha, fungi, molds, RNA polymerase II, systematics.

12. Described are nucleic acid molecules encoding enzymes having fructosyl polymerase activity.

13. RNA polymerase II synthesizes precursors of mRNAs and most snRNA and microRNAs.

14. Amplifiers for polymerase chain reaction (PCR) used to amplify DNA for laboratory use

15. The samples were tested for influenza virus ribonucleic acid (RNA) using polymerase chain reaction.

16. TOPO® Cloning utilizes the Taq polymerase which naturally leaves a single adenosine (A) …

17. DNA can also be amplified using a procedure called the polymerase chain reaction (PCR).

18. Biochemist Kary Mullis won the 1993 Nobel Prize in Chemistry for inventing the polymerase chain reaction

19. A polymerase chain reaction method for measuring Astragalus content in a polyherbal preparation has been published

20. Furthermore, poly(ADP-ribose) polymerase (PARP) inhibitors could further expand the treatment options for recurrent disease.

21. The long segment (around 7200 nucleotides in length) encodes the viral polymerase and a zinc-binding protein.

22. Poly(adp-ribose) polymerase ('parp') inhibitors, methods and pharmaceutical compositions for treating neural or cardiovascular tissue damage

23. Method for detecting metal ions using unnatural activity of nucleic acid polymerase, and logic gate using same

24. Genetic analysis of the samples was performed using advanced methods like the Polymerase Chain Reaction (PCR) technique.

25. The triphosphorylated form of ACV serves as both a substrate and inhibitor of the herpes DNA polymerase.

26. The present invention relates to a method for detecting single nucleotide polymorphism (SNP) using a feature that the 5'-flap endonuclease (FEN) activity of DNA polymerase is inhibited when a probe complementarily binds to the end of a polymerase chain reaction (PCR) product.

27. The Curative SARS-CoV-2 Assay is a real-time reverse transcription polymerase chain reaction (rRT-PCR) test

28. Confirmed cases are those that have positive results from diagnostic, confirmatory polymerase chain reaction (PCR) tests or nucleic

29. PabpolB is already marketed under a brand name, Isis to amplify DNA using the polymerase chain reaction (PCR).

30. The researchers used polymerase chain reaction to amplify Tn916-like cTns followed by restriction fragment length polymorphism analysis.

31. Individual Alleles are amplified using the polymerase chain reaction (PCR) and measured following capillary electrophoresis (CE) separation and detection

32. The sequence of nucleotides for the A, B and O genes was amplified by the polymerase chain reaction (PCR).

33. Exons 10, 11, 13, 14, 15 and 16 of the RET proto-oncogene were amplified in polymerase chain reactions.

34. We report here the crystal structure of RNA polymerase II in the third state, the reverse translocated, or “Backtracked” state

35. The present invention relates to a freeze-drying reagent composition for a polymerase chain reaction, and a preparation method therefor.

36. 21 In summary, we have identified two ORFs which encode RNA polymerase subunits with considerable similarity to their cellular counterparts.

37. A polymerase chain reaction (PCR) assay has been developed to detect pineapple Bacilliform virus (PBV) in extracts from infected plants

38. Diagnosis was based on universal polymerase chain reaction from a cortical brain biopsy, followed by sequencing of the amplified rDNA gene.

39. Polymerase Chain Reaction (PCR) was used to amplify the genomic regions of interest (exon 2 MHC class genes DRA and DRB).

40. A strand-displacing DNA polymerase initiates synthesis and 2 of the primers form loop structures to facilitate subsequent rounds of Amplification.

41. The Arog gene was amplified by polymerase chain reaction(PCR) from strain K-12 and a mutant strain resistant to phenylalanine analogues

42. This technology has been demonstrated with polymerase chain reaction amplified DNA including different sequences to identify a mutation in the CF gene.

43. Samples of DNA were first amplified using the semi-automated polymerase chain reaction and then subjected to a Taqman drug response analysis.

44. Objective: To characterize the microbial etiology of chronic suppurative otitis media comparing the methods of classical Bacteriological culture and polymerase chain reaction

45. The repetitive polymerase chain reaction (rep-PCR) technique was utilised to amplify the DNA from some 140 bacterial isolates from selected fish farms.

46. Some samples were also analyzed by restriction fragment length polymorphism (RFLP) analysis of reverse transcription polymerase chain reaction (RT-PCR)-amplified DNA fragments.

47. Learn about isothermal Amplification, compare differences between LAMP and PCR, and how Phi29 DNA polymerase is the main enzyme of choice for WGA

48. Molecular biology Archaea are of interest in biotechnology as they have unique biochemical features (e.g., enzymes of theromophiles, such as Taq polymerase, the

49. Subsequently, polymerase chain reaction (PCR) method was employed to amplify the minute amounts of DNA in the biological samples and strengthen the signal.

50. The present invention relates to a method for detecting metal ions using unnatural activity of nucleic acid polymerase and a logic gate using same.

51. The addition of the Adenines is catalyzed by the enzyme poly (A) polymerase, which recognizes the sequence AAUAAA as a signal for the addition

52. Naturejobs - All Jobs In this study, we present X-ray structures of a DNA polymerase caught while incorporating a nucleotide opposite an Abasic site

53. Symbol: Atmin: Name: ATM interactor: RGD ID: 1305781: Description: Predicted to have DNA-binding transcription activator activity, RNA polymerase II-specific; dynein complex bindi

54. The method ARDRA-ITS uses the internal transcribed spacer (ITS) of the ribosomal DNA (rDNA) which is amplified by the polymerase chain reaction (PCR).

55. According to the invention, the method for detecting metal ions using unnatural activity of nucleic acid polymerase can reduce cost and detect metal ions easily.

56. 20 Objective Polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP) assay was applied to molecular typing of resistance-associated esterase genes of Culex pipiens complex.

57. Inhibitors of poly(ADP-ribose)polymerase having a structure of Formula (I), ways to make them and methods of treating patients using them are disclosed.

58. The method involves using polymerase chain reaction nucleic acid primers to amplify target microbial sequences and thereafter detecting the presence or absence of amplicons using microsphere agglutination.

59. HLA typing was performed using polymerase chain reaction/restriction fragment-length polymorphism (PCR/RFLP) and PCR/sequence-specific primer (PCR/SSP) methods in 100 Kurds and 100 Azeris.

60. ‘appropriate diagnostic test’ means a real-time quantitative polymerase chain reaction (qPCR) assay containing species-specific STerF and STerR primers amplifying a 119 nucleotide long fragment of Bsal DNA;

61. S phase-specific Antimetabolite (of pyrimidine) that is converted to a 5'-mononucleotide (AraCMP), and then to AraCTP, which competitively inhibits DNA polymerase and results in blockade of DNA synthesis

62. A method is described using the polymerase chain reaction (PCR) to amplify defined nucleic acid strands in individual cellsin situ in conventional smears of bone marrow and peripheral cells.

63. Random amplified polymorphic DNA (RAPD) analysis was used to evaluate the genetic diversity of the isolates. In this analysis, polymerase chain reaction was performed by using four random decamer primers.

64. Design/setting/patients: Bacteriological analysis by classical culture and by molecular polymerase chain reaction of 35 effusion otitis samples from patients with cleft lip and palate attending the Hospital for

65. Samples of lymphocytic genomic DNA were amplified with polymerase chain reaction, and analysis of the coding exons including the flanking intron/UTR sequences of the OPA-1 gene was performed.

66. The purified enzyme had an absolute requirement for DNA and was inhibited by actinomycin D and other known inhibitors of DNA-dependent RNA polymerase, but not by rifamycin or rifampicin.

67. The Arbitrarily primed polymerase chain reaction (AP-PCR) is a PCR-based DNA fingerprinting technique using primers whose nucleotide sequence is Arbitrarily chosen (Welsh and McClelland 1990; Williams et al

68. Nail specimens and skin scrapings were investigated for fungi using Blancophor® preparation, and cultured. In addition to conventional diagnostics, PCR (polymerase chain reaction) for detection of dermatophyte DNA was employed.

69. For the recently described serotype 15 of biotype I and serotypes 13 and 14 of biotype II of Actinobacillus pleuropneumoniae, fhuA and hgbA were detected by polymerase chain reaction and DNA sequencing.

70. Alizarine derivatives as new dual inhibitors of the HIV-1 reverse transcriptase-associated DNA polymerase and RNase H activities effective also on the RNase H activity of non-nucleoside resistant reverse transcriptases

71. Buffers are commonly used in research labs, especially in applications involving protein electrophoresis, polymerase chain reaction and Western blotting.Buffers are vital components for modeling biological systems and have many uses in cell culture, molecular

72. Arenaviruses use a cap snatching strategy to gain the cap structures from the cellular mRNAs, and it is mediated by the endonuclease activity of the L polymerase and the cap binding activity of NP.

73. The most commonly utilized Confirmatory tests include periodic acid-Schiff (PAS) staining, nail culture, in-office potassium hydroxide (KOH) preparation of nail clippings, or polymerase chain reaction (PCR) [5, 6], each conferring unique strengths and limitations.

74. The IBX Test being offered by Concentric by Ginkgo is a PCR (polymerase chain reaction)-based test that is designed to detect the virus that causes COVID-19 in respiratory specimens, for example nasal, oral swabs, or saliva.

75. To test this hypothesis, 34 human specimens obtained during carotid endarterectomy or bypass procedures were examined by use of specific oligonucleotide primers for Porphyromonas gingivalis, Prevotella intermedia, Actinobacillus actinomycetemcomitans and Bacteroides forsythus in polymerase chain reaction (PCR) assays.

76. Polymerase chain reaction (PCR) was therefore performed from pretreatment biopsy specimens from lesional skin of 36 erythema migrans patients (m:f=15:21, mean age 49 years) and seven acrodermatitis chronica atrophicans patients (m:f=0:7, mean age 59 years), respectively.

77. If the result of either duplicate test is reactive, the specimen is reported as repeatedly reactive and undergoes confirmatory testing with a more specific supplemental test (e.g., a polymerase chain reaction (PCR), western blot or, less commonly, an immunofluorescence assay (IFA)).

78. Evidently inspired by his dad, Arthur Kornberg, who won the Nobel prize in 1959 for his work on describing the DNA polymerase enzyme that facilitates DNA replication, young Roger published a research paper in 2001 that set the scientific community abuzz.

79. The application further describes a method for diprotection of RNA with aqueous ethylamine, a method for synthesis of a basic ribonucleoside mimetics, and transcription units comprising an RNA polymerase II promoter, a U6 small nuclear promoter, or an adenovirus VA1 promoter system.

80. Codon optimization is a common strategy to increase heterologous expression levels, based on the premise that using Codons frequently used in the expression host should increase expression yields by avoiding a shortage of charged tRNAs or transcriptional arrest of the RNA polymerase.