Transcribed Spacers(전사된 스페이서)란 무엇입니까?
Transcribed Spacers 전사된 스페이서 - Additionally, Fpr4 and TRAMP5 negatively regulate RNAs from the nontranscribed spacers of ribosomal DNA. [1] The effective markers for trees of the Aigeiros Duby section have recently been developed using the polymorphism of 5S rDNA non-transcribed spacers (NTSs). [2] Amongst these are the non-transcribed spacers of ribosomal DNA where either paralog is sufficient to establish chromatin that is both transcriptionally silent and refractory to recombination. [3] The effective markers for trees of the Aigeiros Duby section have recently been developed using the polymorphism of 5S rDNA non-transcribed spacers (NTSs). [4]또한, Fpr4 및 TRAMP5는 리보솜 DNA의 전사되지 않은 스페이서로부터 RNA를 음성적으로 조절합니다. [1] Aigeiros Duby 섹션의 나무에 대한 효과적인 마커는 최근 5S rDNA NTS(non-transcribed spacer)의 다형성을 사용하여 개발되었습니다. [2] 이들 중에는 전사적으로 침묵하고 재조합에 불응성인 염색질을 확립하기에 파라로그 중 하나가 충분한 리보솜 DNA의 전사되지 않은 스페이서가 있습니다. [3] Aigeiros Duby 섹션의 나무에 대한 효과적인 마커는 최근 5S rDNA NTS(non-transcribed spacer)의 다형성을 사용하여 개발되었습니다. [4]
translation elongation factor 번역 연신율
The internal transcribed spacers (ITS), part of the translation elongation factor-1α (tef1) and partial β-tubulin (tub2) sequence data were analyzed to investigate the phylogenetic relationships of the new species with other Lasiodiplodia species. [1] Sequence analyses based on the regions of large subunit rRNA (LSU), small subunit rRNA (SSU), translation elongation factor 1-α (TEF) and internal transcribed spacers (ITS) were performed to resolve the phylogenetic relationships of the new taxon in Phaeosphaeriaceae. [2] Fifty fungal isolates were obtained and identified based on morphology and phylogeny, through analysis of the ribosomal DNA internal transcribed spacers (ITS), translation elongation factor 1-alpha (TEF1-alpha), β-tubulin (TUB-2), second largest subunit of RNA polymerase (RPB2), glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the mating type locus MAT1–2 (ApMAT) partial gene sequences. [3] 8S nuclear ribosomal gene with the two flanking internal transcribed spacers (ITS), translation elongation factor (EF-1α), calmodulin (CAM), partial RNA polymerase largest subunit (RPB1) and partial RNA polymerase second largest subunit (RPB2), was generated to distinguish species within the FIESC. [4]내부 전사된 스페이서(ITS), 번역 신장 인자-1α(tef1)의 일부 및 부분 β-튜불린(tub2) 서열 데이터를 분석하여 새로운 종과 다른 Lasiodiplodia 종 간의 계통 발생 관계를 조사했습니다. [1] 대형 서브유닛 rRNA(LSU), 소형 서브유닛 rRNA(SSU), 번역 신장 인자 1-α(TEF) 및 내부 전사 스페이서(ITS) 영역을 기반으로 한 서열 분석을 수행하여 Phaeosphaeriaceae의 새로운 분류군의 계통 발생 관계를 해결했습니다. . [2] nan [3] nan [4]
3 phosphate dehydrogenase 3인산 탈수소효소
Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), histone-3 (HIS3), DNA lyase (APN2), intergenic spacer between DNA lyase and the mating-type locus MAT1-2-1 (APN2/MAT-IGS), and intergenic spacer between GAPDH and a hypothetical protein (GAP2-IGS) have the properties of good barcodes, whereas sequences of actin (ACT), chitin synthase (CHS-1) and nuclear rDNA internal transcribed spacers (nrITS) are not able to distinguish most species. [1] Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), histone-3 (HIS3), DNA lyase (APN2), intergenic spacer between DNA lyase and the mating-type locus MAT1-2-1 (APN2/MAT-IGS), and intergenic spacer between GAPDH and a hypothetical protein (GAP2-IGS) have the properties of good barcodes, whereas sequences of actin (ACT), chitin synthase (CHS-1) and nuclear rDNA internal transcribed spacers (nrITS) are not able to distinguish most species. [2] To confirm the species identification, six DNA regions of the randomly selected strain AACAWY203DRT5 were amplified by polymerase chain reaction and sequenced: rDNA internal transcribed spacers regions (ITS), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), calmodulin (CAL), chitin synthase (CHS) (Gan et al. [3]Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), histone-3 (HIS3), DNA lyase (APN2), intergenic spacer between the DNA lyase and the mating-type locus MAT1-2-1 (APN2/MAT-IGS), intergenic spacer GAPDH와 가상 단백질(GAP2-IGS) 사이에는 좋은 바코드의 특성이 있는 반면, 액틴(ACT), 키틴 합성효소(CHS-1) 및 핵 rDNA 내부 전사 스페이서(nrITS)의 서열은 대부분의 종을 구별할 수 없습니다. [1] Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), histone-3 (HIS3), DNA lyase (APN2), intergenic spacer between the DNA lyase and the mating-type locus MAT1-2-1 (APN2/MAT-IGS), intergenic spacer GAPDH와 가상 단백질(GAP2-IGS) 사이에는 좋은 바코드의 특성이 있는 반면, 액틴(ACT), 키틴 합성효소(CHS-1) 및 핵 rDNA 내부 전사 스페이서(nrITS)의 서열은 대부분의 종을 구별할 수 없습니다. [2] 종 식별을 확인하기 위해 무작위로 선택된 AACAWY203DRT5 균주의 6개 DNA 영역을 중합효소 연쇄 반응에 의해 증폭하고 시퀀싱했습니다: rDNA 내부 전사 스페이서 영역(ITS), 글리세르알데히드-3-포스페이트 탈수소효소(GAPDH), 칼모듈린(CAL), 키틴 합성효소 (CHS) (Gan et al. [3]
fungal root associated 곰팡이 뿌리 관련
Using plants grown in natural soil and community profiling of bacterial 16S rRNA genes and fungal internal transcribed spacers (ITSs), we examined the role of the Lotus symbiosis genes RAM1, NFR5, SYMRK, and CCaMK in structuring bacterial and fungal root-associated communities. [1] Using plants grown in natural soil and community profiling of bacterial 16S rRNA genes and fungal internal transcribed spacers (ITS), we examined the role of the Lotus symbiosis genes RAM1, NFR5, SYMRK, and CCaMK in structuring bacterial and fungal root-associated communities. [2] Using plants grown in natural soil and community profiling of bacterial 16S rRNA genes and fungal internal transcribed spacers (ITS), we examined here the role of the Lotus symbiosis genes RAM1, NFR5, SYMRK, and CCaMK in structuring bacterial and fungal root-associated communities. [3]자연 토양에서 자란 식물과 박테리아 16S rRNA 유전자 및 곰팡이 내부 전사 스페이서(ITS)의 커뮤니티 프로파일링을 사용하여 우리는 박테리아 및 곰팡이 뿌리 관련 커뮤니티를 구조화하는 로터스 공생 유전자 RAM1, NFR5, SYMRK 및 CCaMK의 역할을 조사했습니다. [1] 자연 토양에서 자란 식물과 박테리아 16S rRNA 유전자 및 곰팡이 내부 전사 스페이서(ITS)의 커뮤니티 프로파일링을 사용하여 우리는 박테리아 및 곰팡이 뿌리 관련 커뮤니티를 구조화하는 로터스 공생 유전자 RAM1, NFR5, SYMRK 및 CCaMK의 역할을 조사했습니다. [2] 자연 토양에서 자란 식물과 박테리아 16S rRNA 유전자 및 곰팡이 내부 전사 스페이서(ITS)의 커뮤니티 프로파일링을 사용하여 여기에서 우리는 박테리아 및 곰팡이 뿌리 관련 커뮤니티를 구조화하는 로터스 공생 유전자 RAM1, NFR5, SYMRK 및 CCaMK의 역할을 조사했습니다. . [3]
nuclear ribosomal internal 핵 리보솜 내부
Diaporthe asparagi (Phomopsis asparagi) was identified based on molecular analysis of the nuclear ribosomal internal transcribed spacers (ITS), while D. [1] Molecular studies, based on the nuclear ribosomal internal transcribed spacers (nrITS), chromosome number data and pollen morphology, support the morphological results. [2] Plastid DNA (trnH–psbA; 674 individuals from 34 populations) and nuclear ribosomal internal transcribed spacers (ITS; 214 individuals from 30 populations) were sequenced to assess genetic diversity, genetic differentiation, population genetic structure, and demographic patterns. [3]Diaporthe asparagi(Phomopsis asparagi)는 핵 리보솜 내부 전사 스페이서(ITS)의 분자 분석을 기반으로 식별된 반면 D. [1] 핵 리보솜 내부 전사 스페이서(nrITS), 염색체 수 데이터 및 꽃가루 형태를 기반으로 한 분자 연구는 형태학적 결과를 뒷받침합니다. [2] nan [3]
second largest subunit 두 번째로 큰 소단위
Aside from morphological and chemotaxonomic studies, a multi-locus phylogenetic analysis using internal transcribed spacers regions (ITS) and the large subunit (LSU) of the ribosomal DNA, the second largest subunit of the RNA polymerase (RPB2), and beta-tubulin (TUB2) genes was performed. [1] Molecular phylogenetic analyses, based on the data of the internal transcribed spacers (ITS) and the large subunit (LSU) of the nuclear ribosomal DNA, and the second largest subunit of RNA polymerase II (rbp2) genes, also support the finding that C. [2]형태학 및 화학분류학 연구 외에도 내부 전사된 스페이서 영역(ITS)과 리보솜 DNA의 큰 소단위(LSU), RNA 중합효소(RPB2)의 두 번째로 큰 소단위 및 베타-튜불린( TUB2) 유전자를 수행하였다. [1] 핵 리보솜 DNA의 내부 전사된 스페이서(ITS)와 큰 소단위체(LSU), RNA 중합효소 II(rbp2) 유전자의 두 번째로 큰 소단위체의 데이터를 기반으로 한 분자 계통발생학적 분석도 C. [2]
Internal Transcribed Spacers 내부 전사 스페이서
Comparisons were based on conidial and pycnidial morphology and multilocus sequence analysis of actin (ACT), β-tubulin (BT), calmodulin (CAL), nuc rDNA internal transcribed spacers (ITS1-5. [1] Aside from morphological and chemotaxonomic studies, a multi-locus phylogenetic analysis using internal transcribed spacers regions (ITS) and the large subunit (LSU) of the ribosomal DNA, the second largest subunit of the RNA polymerase (RPB2), and beta-tubulin (TUB2) genes was performed. [2] Molecular analysis based on obtained sequences (MH479426) of the rDNA internal transcribed spacers (ITS1 and ITS4) resulted more than 92 per cent identical to ITS sequence of C. [3] 8S, and 28S rDNA) and two internal transcribed spacers (ITS1 and ITS2). [4] Finally, we observed small-RNAs derived from internal transcribed spacers (ITSs) of a U3 snoRNA loci that via complementarity binding, may be involved in the biosynthesis of U3-DII snoRNAs. [5] The internal transcribed spacers (ITS), part of the translation elongation factor-1α (tef1) and partial β-tubulin (tub2) sequence data were analyzed to investigate the phylogenetic relationships of the new species with other Lasiodiplodia species. [6] The phylogenetic relationships of 42 species of cloacinine nematodes belonging to three tribes (Coronostrongylinea, Macropostrongylinea and Zoniolaiminea) were examined based on sequence data of the first and second internal transcribed spacers (ITS-1 and ITS-2) of the nuclear ribosomal DNA. [7] The internal transcribed spacers (ITS) of the rDNA cistron are the most commonly used DNA barcoding region in Fungi [11], and rely on concerted evolution to homogenize the rDNA array leading to a “barcode gap” [12]. [8] Sequences of the internal transcribed spacers (ITSs) of nuclear ribosomal DNA (nrDNA) were studied in 15 Tunisian date palm accessions (Phoenix dactylifera L. [9] In the present study, we examined bacterial and fungal communities in the rhizosphere of wheat and canola at six paired locations on fall and spring sampling dates using high-throughput sequencing of marker genes (bacterial 16S rRNA gene and fungal internal transcribed spacers). [10] Cultures identified as Diaporthe based on morphological features were further identified to species level by sequencing the internal transcribed spacers (ITS) 1 and 2 and 5. [11] Specific LAMP assays based on rDNA internal transcribed spacers 1 or 2 sequences, considering intraspecies variability at these loci, were developed for Aedes aegypti, Aedes albopictus, Aedes japonicus, Aedes koreicus and the indigenous Aedes geniculatus. [12] Genomic approaches are based mainly on detecting amplicons of ribosomal RNA genes, and internal transcribed spacers are gradually gaining popularity in clinical practices. [13] 1–8), but slightly lower than those of the internal transcribed spacers (ITS). [14] Sequence data from amplified internal transcribed spacers (ITS) 2 region with fungal-specific primers exposed 83,417 sequences belonging to 7 operational taxonomic units (OTUs). [15] Sequence analyses based on the regions of large subunit rRNA (LSU), small subunit rRNA (SSU), translation elongation factor 1-α (TEF) and internal transcribed spacers (ITS) were performed to resolve the phylogenetic relationships of the new taxon in Phaeosphaeriaceae. [16] Fifty fungal isolates were obtained and identified based on morphology and phylogeny, through analysis of the ribosomal DNA internal transcribed spacers (ITS), translation elongation factor 1-alpha (TEF1-alpha), β-tubulin (TUB-2), second largest subunit of RNA polymerase (RPB2), glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and the mating type locus MAT1–2 (ApMAT) partial gene sequences. [17] Phylogenies inferred from 28S, nuc rDNA internal transcribed spacers (ITS1-5. [18] Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), histone-3 (HIS3), DNA lyase (APN2), intergenic spacer between DNA lyase and the mating-type locus MAT1-2-1 (APN2/MAT-IGS), and intergenic spacer between GAPDH and a hypothetical protein (GAP2-IGS) have the properties of good barcodes, whereas sequences of actin (ACT), chitin synthase (CHS-1) and nuclear rDNA internal transcribed spacers (nrITS) are not able to distinguish most species. [19] The collected strains were identified by sequencing several regions, including internal transcribed spacers, and determined their susceptibility to the antifungals itraconazole, voriconazole, and amphotericin B. [20] The effectiveness of a polyphenol-based cluster analysis was compared to molecular markers (internal transcribed spacers, ITS1 and ITS2) to unequivocally discern the two apples. [21] Phylogenetic evidence presented here resolves the relationship of Phaeochorella within the Sordariomycetes, based on a multilocus analysis of partial nuc rDNA large subunit (28S) and internal transcribed spacers (ITS1-5. [22] The phylogenetic tree based on internal transcribed spacers of rDNA sequences using Bayesian and Maximum Likelihood methods showed that G. [23] The internal transcribed spacers (ITS) of the rDNA cistron are the most commonly used DNA barcoding region in Fungi [1]. [24] altissima internal transcribed spacers of 35S rDNA were long and intrinsically repetitive while in G. [25] Identification of the Pythium species was achieved by examining their morphological features and sequences analysis of internal transcribed spacers (ITS) and cytochrome oxidase subunit 2 gene (Cox II). [26] Using plants grown in natural soil and community profiling of bacterial 16S rRNA genes and fungal internal transcribed spacers (ITSs), we examined the role of the Lotus symbiosis genes RAM1, NFR5, SYMRK, and CCaMK in structuring bacterial and fungal root-associated communities. [27] Using plants grown in natural soil and community profiling of bacterial 16S rRNA genes and fungal internal transcribed spacers (ITS), we examined the role of the Lotus symbiosis genes RAM1, NFR5, SYMRK, and CCaMK in structuring bacterial and fungal root-associated communities. [28] Molecular phylogenetic analyses, based on the data of the internal transcribed spacers (ITS) and the large subunit (LSU) of the nuclear ribosomal DNA, and the second largest subunit of RNA polymerase II (rbp2) genes, also support the finding that C. [29] Diaporthe asparagi (Phomopsis asparagi) was identified based on molecular analysis of the nuclear ribosomal internal transcribed spacers (ITS), while D. [30] Using three chloroplast markers and nuclear internal transcribed spacers of ribosomalDNA(ITS), we present a phylogeny of the Begonia sections Casparya and Semibegoniella (Begoniaceae) and representative species of related sections. [31] Using plants grown in natural soil and community profiling of bacterial 16S rRNA genes and fungal internal transcribed spacers (ITS), we examined here the role of the Lotus symbiosis genes RAM1, NFR5, SYMRK, and CCaMK in structuring bacterial and fungal root-associated communities. [32] This maturation process involves a large set of accessory proteins as well as ribonucleases, responsible for removal of the external and internal transcribed spacers from the pre-rRNA. [33] With the objective to evidence the relation between apomixes and polyembryony, were used sequences of internal transcribed spacers (ITS), and intergenic spacers (IGS) and amplification of simple repeated sequences (SSR). [34] The validated SNPs were used to check cockles that were suggested to be hybrids by a claimed diagnostic tool based on the internal transcribed spacers of the ribosomal RNA. [35] A meta-barcoding approach based on Illumina sequencing of internal transcribed spacers (ITS1 and ITS2) was carried out on DNA extracted from root samples (fine roots and ECM root tips separately). [36] Sequences of the Cytochrome oxidase II gene and fragments of the Internal Transcribed Spacers 1 for both species are also provided. [37] Partial DNA sequences of the mitochondrial gene cytochrome c oxidase subunit I (cox 1) and the internal transcribed spacers (ITS1, 5. [38] On the other hand, nucleotide sequence analysis of internal transcribed spacers (ITS) of rDNA has proved to be a useful method for identification of dermatophytes. [39] For the first time in Pakistan, adult flukes were morphologically characterized and the sequence variation in the nuclear ribosomal DNA (rDNA) region, including the first internal transcribed spacers (ITS1) and the 5. [40] The DNA sequencing, which includes two non-coding regions designated as the internal transcribed spacers (ITS1 and ITS2) and the 5. [41] aestivum that is grown both under N/P fertilization and in conditions of extreme N/P-starvation, were taxonomically described and compared (bacterial 16S rRNA genes and fungal Internal Transcribed Spacers—ITS). [42] All major splits among Brassicaceae lineages were used in BEAST analyses of individually analysed 48 tribes comprising 2101 taxa in total using the internal transcribed spacers of nuclear ribosomal DNA. [43] Partial sequences of the 18S and internal transcribed spacers (ITS1-5. [44] formosanus on Okinawa Island, I developed a diagnostic polymerase chain reaction method using primer sets specific to the nuclear ribosomal DNA sequences consisting of the internal transcribed spacers (ITS1 and ITS2) and 5. [45] A phylogenetic analysis, performed using combined internal transcribed spacers (ITS), the large subunit (LSU) of ribosomal DNA (rDNA) regions, and a part of the histone 3 (H3) gene, lends support to our the finding that A. [46] To fill this knowledge gap, we sequenced and determined the internal transcribed spacers of ribosomal DNA (ITS rDNA) and the complete mitochondrial (mt) genome of S. [47] The diversity of the bacterial collection was evaluated by amplification of the internal transcribed spacers between the 16S and the 23S rRNA genes (ITS-PCR) and by 16S rRNA sequencing. [48] Our phylogenetic analyses, inferred from partial nucleotide sequences including the internal transcribed spacers (ITS) 1 and 2 with the 5. [49] Previous studies of the Internal Transcribed Spacers of the nuclear ribosomal DNA (ITS) in sections Quercus (white oaks), Protobalanus (intermediate or golden cup oaks), Cerris (Cerris oaks), and Ilex (Ilex oaks) suggest that ITS regions undergo full concerted evolution in oaks; however, ITS evolution patterns in red oaks (section Lobatae) are unknown due to scant representation in published work. [50]비교는 분생자 및 자소체 형태와 액틴(ACT), β-튜불린(BT), 칼모듈린(CAL), nuc rDNA 내부 전사 스페이서(ITS1-5. [1] 형태학 및 화학분류학 연구 외에도 내부 전사된 스페이서 영역(ITS)과 리보솜 DNA의 큰 소단위(LSU), RNA 중합효소(RPB2)의 두 번째로 큰 소단위 및 베타-튜불린( TUB2) 유전자를 수행하였다. [2] nan [3] nan [4] nan [5] 내부 전사된 스페이서(ITS), 번역 신장 인자-1α(tef1)의 일부 및 부분 β-튜불린(tub2) 서열 데이터를 분석하여 새로운 종과 다른 Lasiodiplodia 종 간의 계통 발생 관계를 조사했습니다. [6] nan [7] nan [8] nan [9] nan [10] nan [11] rDNA 내부 전사된 스페이서 1 또는 2 서열을 기반으로 하는 특정 LAMP 분석은 Aedes aegypti, Aedes albopictus, Aedes japonicus, Aedes koreicus 및 토착 Aedes geniculatus에 대해 개발되었습니다. [12] nan [13] nan [14] nan [15] 대형 서브유닛 rRNA(LSU), 소형 서브유닛 rRNA(SSU), 번역 신장 인자 1-α(TEF) 및 내부 전사 스페이서(ITS) 영역을 기반으로 한 서열 분석을 수행하여 Phaeosphaeriaceae의 새로운 분류군의 계통 발생 관계를 해결했습니다. . [16] nan [17] nan [18] Glyceraldehyde-3-phosphate dehydrogenase (GAPDH), histone-3 (HIS3), DNA lyase (APN2), intergenic spacer between the DNA lyase and the mating-type locus MAT1-2-1 (APN2/MAT-IGS), intergenic spacer GAPDH와 가상 단백질(GAP2-IGS) 사이에는 좋은 바코드의 특성이 있는 반면, 액틴(ACT), 키틴 합성효소(CHS-1) 및 핵 rDNA 내부 전사 스페이서(nrITS)의 서열은 대부분의 종을 구별할 수 없습니다. [19] nan [20] nan [21] nan [22] nan [23] nan [24] nan [25] nan [26] 자연 토양에서 자란 식물과 박테리아 16S rRNA 유전자 및 곰팡이 내부 전사 스페이서(ITS)의 커뮤니티 프로파일링을 사용하여 우리는 박테리아 및 곰팡이 뿌리 관련 커뮤니티를 구조화하는 로터스 공생 유전자 RAM1, NFR5, SYMRK 및 CCaMK의 역할을 조사했습니다. [27] 자연 토양에서 자란 식물과 박테리아 16S rRNA 유전자 및 곰팡이 내부 전사 스페이서(ITS)의 커뮤니티 프로파일링을 사용하여 우리는 박테리아 및 곰팡이 뿌리 관련 커뮤니티를 구조화하는 로터스 공생 유전자 RAM1, NFR5, SYMRK 및 CCaMK의 역할을 조사했습니다. [28] 핵 리보솜 DNA의 내부 전사된 스페이서(ITS)와 큰 소단위체(LSU), RNA 중합효소 II(rbp2) 유전자의 두 번째로 큰 소단위체의 데이터를 기반으로 한 분자 계통발생학적 분석도 C. [29] Diaporthe asparagi(Phomopsis asparagi)는 핵 리보솜 내부 전사 스페이서(ITS)의 분자 분석을 기반으로 식별된 반면 D. [30] nan [31] 자연 토양에서 자란 식물과 박테리아 16S rRNA 유전자 및 곰팡이 내부 전사 스페이서(ITS)의 커뮤니티 프로파일링을 사용하여 여기에서 우리는 박테리아 및 곰팡이 뿌리 관련 커뮤니티를 구조화하는 로터스 공생 유전자 RAM1, NFR5, SYMRK 및 CCaMK의 역할을 조사했습니다. . [32] nan [33] nan [34] nan [35] nan [36] Cytochrome oxidase II 유전자의 서열과 두 종에 대한 Internal Transcribed Spacers 1의 단편도 제공됩니다. [37] nan [38] nan [39] nan [40] nan [41] nan [42] nan [43] nan [44] nan [45] nan [46] nan [47] nan [48] nan [49] nan [50]
transcribed spacers region 전사된 스페이서 영역
Aside from morphological and chemotaxonomic studies, a multi-locus phylogenetic analysis using internal transcribed spacers regions (ITS) and the large subunit (LSU) of the ribosomal DNA, the second largest subunit of the RNA polymerase (RPB2), and beta-tubulin (TUB2) genes was performed. [1] To confirm the species identification, six DNA regions of the randomly selected strain AACAWY203DRT5 were amplified by polymerase chain reaction and sequenced: rDNA internal transcribed spacers regions (ITS), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), calmodulin (CAL), chitin synthase (CHS) (Gan et al. [2]형태학 및 화학분류학 연구 외에도 내부 전사된 스페이서 영역(ITS)과 리보솜 DNA의 큰 소단위(LSU), RNA 중합효소(RPB2)의 두 번째로 큰 소단위 및 베타-튜불린( TUB2) 유전자를 수행하였다. [1] 종 식별을 확인하기 위해 무작위로 선택된 AACAWY203DRT5 균주의 6개 DNA 영역을 중합효소 연쇄 반응에 의해 증폭하고 시퀀싱했습니다: rDNA 내부 전사 스페이서 영역(ITS), 글리세르알데히드-3-포스페이트 탈수소효소(GAPDH), 칼모듈린(CAL), 키틴 합성효소 (CHS) (Gan et al. [2]
transcribed spacers 1 전사된 스페이서 1
Specific LAMP assays based on rDNA internal transcribed spacers 1 or 2 sequences, considering intraspecies variability at these loci, were developed for Aedes aegypti, Aedes albopictus, Aedes japonicus, Aedes koreicus and the indigenous Aedes geniculatus. [1] Sequences of the Cytochrome oxidase II gene and fragments of the Internal Transcribed Spacers 1 for both species are also provided. [2]rDNA 내부 전사된 스페이서 1 또는 2 서열을 기반으로 하는 특정 LAMP 분석은 Aedes aegypti, Aedes albopictus, Aedes japonicus, Aedes koreicus 및 토착 Aedes geniculatus에 대해 개발되었습니다. [1] Cytochrome oxidase II 유전자의 서열과 두 종에 대한 Internal Transcribed Spacers 1의 단편도 제공됩니다. [2]