Highly degenerate, inosine-containing primers specifically amplify rare cDNA using the polymerase chain reaction.
about
Universal primers that amplify RNA from all three flavivirus subgroupsMolecular cloning of an atypical voltage-gated sodium channel expressed in human heart and uterus: evidence for a distinct gene familyMolecular cloning and protein structure of a human blood group Rh polypeptideSelective amplification of an mRNA and related pseudogene for a human ADP-ribosylation factor, a guanine nucleotide-dependent protein activator of cholera toxinNovel actin crosslinker superfamily member identified by a two step degenerate PCR procedureIdentification of a cytochrome P450 gene by reverse transcription--PCR using degenerate primers containing inosineMolecular cloning and expression of ps20 growth inhibitor. A novel WAP-type "four-disulfide core" domain protein expressed in smooth muscleUnveiling of the diversity of Prasinoviruses (Phycodnaviridae) in marine samples by using high-throughput sequencing analyses of PCR-amplified DNA polymerase and major capsid protein genesMolecular cloning of PARP (proline/arginine-rich protein) from human cartilage and subsequent demonstration that PARP is a fragment of the NH2-terminal domain of the collagen α2(XI) chainDeep sequencing of a dimethylsulfoniopropionate-degrading gene (dmdA) by using PCR primer pairs designed on the basis of marine metagenomic data.Cloning of the immunological repertoire in Escherichia coli for generation of monoclonal catalytic antibodies: construction of a heavy chain variable region-specific cDNA library.Bacterial biota in reflux esophagitis and Barrett's esophagus.Amplification of nucleic acids by polymerase chain reaction (PCR) and other methods and their applications.Directional cloning of DNA fragments using deoxyinosine-containing oligonucleotides and endonuclease V.A Unique Primer with an Inosine Chain at the 5'-Terminus Improves the Reliability of SNP Analysis Using the PCR-Amplified Product Length Polymorphism MethodA mouse homolog of the Escherichia coli recA and Saccharomyces cerevisiae RAD51 genes.Two-step polymerase chain reactions and restriction endonuclease analyses detect and differentiate ompA DNA of Chlamydia spp.Detection and strain differentiation of Chlamydia psittaci mediated by a two-step polymerase chain reaction.Bacterial biota in the human distal esophagus.Molecular cloning of a human thyrotropin receptor cDNA fragment. Use of highly degenerate, inosine containing primers derived from aligned amino acid sequences of a homologous family of glycoprotein hormone receptors.rpoB gene analysis as a novel strategy for identification of spirochetes from the genera Borrelia, Treponema, and Leptospira.Amplification of DNA polymerase gene fragments from viruses infecting microalgae.Evaluation of infection with human immunodeficiency virus type 1 by using nonisotopic solution hybridization for detection of polymerase chain reaction-amplified proviral DNA.New approaches to the diagnosis of oral soft-tissue disease of viral origin.The polymerase chain reaction: applications for the detection of foodborne pathogens.Clinical applications of the polymerase chain reaction.Alternative mRNA Processing Occurs in the Variable Region of the Pro-1(XI) and Pro-2(XI) Collagen Chains
P2860
Q24286946-011AF404-D8AC-4CC4-BEE5-C24EDE4A84CBQ24336511-840E7707-A0E0-49B3-BE29-21FCD03F2A73Q24557491-6300E7DE-6ED8-4864-A70C-D81277DA790EQ24558739-203AA6BE-DF07-44B0-A162-4D7DFD697604Q28295252-91783091-8E4E-49EF-8FEA-79547C056A73Q28367497-88336852-606A-4143-89AA-0676066DA37DQ28578517-5CC5E5E5-E3CA-44DA-B7C0-F67440BBBFCAQ28657444-B445EB11-5C99-4517-98B3-86092B857FE9Q29396708-0FCC9A5B-F7B5-48CE-AB36-D6CBC2ED7A11Q30492738-43EA5EBB-C8C1-49E0-B129-AE4D6073B7F1Q34293780-5D511D3F-76B7-4F4A-BBFA-7242F923198BQ34514507-A4C1EB88-46E1-47FC-8C31-E90DB2C75C74Q34594233-5F1F1760-0375-4DF2-8CB7-57420E304A9FQ35007311-0D569437-AE49-4F5D-864C-C28C2D5A7D48Q35779284-CC720B82-50F8-4205-A562-1AE4B01BE96AQ36420035-806EE9E0-DCCD-4173-BC05-73F5987511A1Q37119818-CFE95494-780D-47CD-BA90-2C04A2C9C01AQ37242694-36FE34F6-F483-4FA9-BAF8-993359193831Q37356948-5EA6A0E3-D1EC-4473-95B6-1E03C389D5F7Q38340816-578BEF34-9714-4A07-BB15-6E72B1D242FAQ39458158-004BBC3F-F096-4A71-B629-980177A229F8Q39797310-5BB18314-2C90-4B38-9746-D9EBD5AA202BQ40214090-80F6C304-4853-44CC-8D73-13787080AF19Q40789910-6E885D42-4CF6-4E96-B24F-48B1E147D4A1Q41069906-963F52A8-15BD-40DE-9783-79B4094C12C8Q44986699-21B21D17-5C9E-4CB0-A828-FEE8DC398B9BQ55919461-3501724B-3358-4FDF-94D7-13B3AC39C39E
P2860
Highly degenerate, inosine-containing primers specifically amplify rare cDNA using the polymerase chain reaction.
description
1988 nî lūn-bûn
@nan
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
1988年论文
@zh
1988年论文
@zh-cn
name
Highly degenerate, inosine-con ...... the polymerase chain reaction.
@en
type
label
Highly degenerate, inosine-con ...... the polymerase chain reaction.
@en
prefLabel
Highly degenerate, inosine-con ...... the polymerase chain reaction.
@en
P2093
P356
P1476
Highly degenerate, inosine-con ...... the polymerase chain reaction
@en
P2093
P2860
P356
10.1093/NAR/16.22.10932
P577
1988-11-01T00:00:00Z