PorA 6 CAG GAA ACA GCT ATG ACC GCG GAC AAT ACG AGG GCG
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چکیده
regions of the promoter. variation in the spacing between the-10 and-35 protein in Neisseria meningitidis is caused by Variable expression of class 1 outer membrane
منابع مشابه
Nucleotide sequence of the gtfA gene from S. mutans GS-5.
5' AAGCTTCCAC TACCTTGCCA CCCGCAATAA GAACGATTAC TTCTCCCTCG CCTT 54 Kec Pro tie Thr Asn 141 CTACCA CCTAAAGATC TCCCTCTTAT TTTTAGOTTG AACTCGTATA AACCAAAATT AATTACACCA GATAAA ATG CCA ATT ACA AAT -35 -10 BBS fut Lys ThT Hec Leu Il« Thr Tyr Ala Aap Ser Leu Gly Lye Asa Leu Lys Glu Leu Asn Glu A«n H e Glu Agn Tyr AAA ACA ATG TTC ATT ACT TAC GCA CAC ACT TTC OGT AAA AAT TTG AAA CAA TTG AAT GAA AAT ATT GAG...
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Table 1 Designations, targets, and positions of primers for PCR analysis and Southern blot hybridization Primer Target Sequence (5′ – 3′) GenBank accession number Reference saaDF saa 5′-CGT GAT GAA CAG GCT ATT GC-3′ AF399919 [26] saaDR saa 5′-ATG GAC ATG CCT GTG GCA AC-3′ AF399919 [26] subAB-V-for subAB 5′-CTT CCC TCA TTG CCT CAC G-3′ AY258503 This study subAB-V-rev subAB 5′-GGC TGG CCT GTT GTG...
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Supplementary Methods Primers used for genotyping: The α’ promoter silencing system and the drd1 mutant alleles have been described previously (Kanno et al., 2004). The work reported here was carried out using plants carrying the drd1-6 allele. The drd1-6 mutation produces a G to A substitution (TGGTCA to TGATCA), producing a new NdeII restriction enzyme site (/GATC) that can be used for genoty...
متن کاملRapid communication: complete nucleotide sequence of the chicken prolactin gene.
Name of Sequence. Chicken prolactin (PRL) gene. Genus and Species. Gallus gallus (chicken). Origin of Clones. Genomic DNA from Xing Hua Chinese native chickens was used as a template. Primers were designed based on exon/intron junctions of the genomic turkey PRL gene sequence (Kurima et al., 1995). Polymerase chain reaction (PCR) amplifications of the PRL gene were performed by using the follow...
متن کاملNathalie Troffer-Charlier, Vincent Cura, Pierre Hassenboehler, Dino Moras, Jean Cavarelli
Cloning of CARM128-140 The N terminal part of mouse CARM1 (amino-acids 28-140) was PCR amplified from the original GST-CARM1 construct (Chen et al, 1999) and cloned in the expression vector pGGWA (Busso et al, 2005) using the Gateway system (Invitrogen). The primers used for cloning were 5’-GGG GAC AAG TTT GTA CAA AAA AGC AGG CTT CCT GGT GCC ACG CGG TTC TCA TAT GGC TAC AGT GTC TGT GTT CCC-3’ wi...
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تاریخ انتشار 1994