p penneri atcc 33519 Search Results


atcc 33519  (ATCC)
92
ATCC atcc 33519
Atcc 33519, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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proteus penneri  (ATCC)
93
ATCC proteus penneri
List of strains used a
Proteus Penneri, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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racemase leguminosarum polypeptide  (ATCC)
92
ATCC racemase leguminosarum polypeptide
List of strains used a
Racemase Leguminosarum Polypeptide, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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proteus vulgaris  (ATCC)
97
ATCC proteus vulgaris
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Proteus Vulgaris, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


List of strains used a

Journal:

Article Title: Fragmentation of 23S rRNA in Strains of Proteus and Providencia Results from Intervening Sequences in the rrn (rRNA) Genes

doi:

Figure Lengend Snippet: List of strains used a

Article Snippet: Lane 1, P. vulgaris (Pv, SGSC3360); lane 2, P. vulgaris (SA5474); lane 3, P. rettgeri (Pr, SA5473); lane 4, Proteus penneri (Pp, SA5462); lane 5, Proteus mirabilis (Pm, SA5450); lane 6, Morganella morganii (Mm, SA5438); lane 7, P. vulgaris (ATCC 13315, ATCC type strain); lane 8, P. vulgaris (ATCC 29905); lane 9, S. enterica serovar Typhimurium LT2 (Stm, SGSC1412); lane 10, E. coli K-12 (Ec, SA1332). (A) The regions of rrl genes containing IVSs were amplified by PCR, with primers P1 and P2 for helix 25 and primers P3 and P4 for helix 45 (as illustrated in Fig. ).

Techniques:

Agarose gel containing PCR products from amplification of regions of rrl genes containing IVSs and rRNA Northern blots from Proteus and Providencia strains. Lane 1, P. vulgaris (Pv, SGSC3360); lane 2, P. vulgaris (SA5474); lane 3, P. rettgeri (Pr, SA5473); lane 4, Proteus penneri (Pp, SA5462); lane 5, Proteus mirabilis (Pm, SA5450); lane 6, Morganella morganii (Mm, SA5438); lane 7, P. vulgaris (ATCC 13315, ATCC type strain); lane 8, P. vulgaris (ATCC 29905); lane 9, S. enterica serovar Typhimurium LT2 (Stm, SGSC1412); lane 10, E. coli K-12 (Ec, SA1332). (A) The regions of rrl genes containing IVSs were amplified by PCR, with primers P1 and P2 for helix 25 and primers P3 and P4 for helix 45 (as illustrated in Fig. ​Fig.1).1). PCR products were separated by electrophoresis in agarose gels containing ethidium bromide and visualized under UV light. (B) rRNA was isolated by phenol extraction as described in Materials and Methods, separated by glyoxal–DMSO–1.5% agarose gel electrophoresis, blotted to a Hybond-N+ membrane, and stained with methylene blue (23).

Journal:

Article Title: Fragmentation of 23S rRNA in Strains of Proteus and Providencia Results from Intervening Sequences in the rrn (rRNA) Genes

doi:

Figure Lengend Snippet: Agarose gel containing PCR products from amplification of regions of rrl genes containing IVSs and rRNA Northern blots from Proteus and Providencia strains. Lane 1, P. vulgaris (Pv, SGSC3360); lane 2, P. vulgaris (SA5474); lane 3, P. rettgeri (Pr, SA5473); lane 4, Proteus penneri (Pp, SA5462); lane 5, Proteus mirabilis (Pm, SA5450); lane 6, Morganella morganii (Mm, SA5438); lane 7, P. vulgaris (ATCC 13315, ATCC type strain); lane 8, P. vulgaris (ATCC 29905); lane 9, S. enterica serovar Typhimurium LT2 (Stm, SGSC1412); lane 10, E. coli K-12 (Ec, SA1332). (A) The regions of rrl genes containing IVSs were amplified by PCR, with primers P1 and P2 for helix 25 and primers P3 and P4 for helix 45 (as illustrated in Fig. ​Fig.1).1). PCR products were separated by electrophoresis in agarose gels containing ethidium bromide and visualized under UV light. (B) rRNA was isolated by phenol extraction as described in Materials and Methods, separated by glyoxal–DMSO–1.5% agarose gel electrophoresis, blotted to a Hybond-N+ membrane, and stained with methylene blue (23).

Article Snippet: Lane 1, P. vulgaris (Pv, SGSC3360); lane 2, P. vulgaris (SA5474); lane 3, P. rettgeri (Pr, SA5473); lane 4, Proteus penneri (Pp, SA5462); lane 5, Proteus mirabilis (Pm, SA5450); lane 6, Morganella morganii (Mm, SA5438); lane 7, P. vulgaris (ATCC 13315, ATCC type strain); lane 8, P. vulgaris (ATCC 29905); lane 9, S. enterica serovar Typhimurium LT2 (Stm, SGSC1412); lane 10, E. coli K-12 (Ec, SA1332). (A) The regions of rrl genes containing IVSs were amplified by PCR, with primers P1 and P2 for helix 25 and primers P3 and P4 for helix 45 (as illustrated in Fig. ).

Techniques: Agarose Gel Electrophoresis, Amplification, Northern Blot, Electrophoresis, Isolation, Staining

Intervening sequences from individual genes for rRNA of selected Proteus, Providencia, and Salmonella strains. Individual rrl genes were sequenced as described in Materials and Methods, and aligned using CLUSTAL X. The conserved residues are shown by dots, and deletions are shown by spaces. The consensus sequence is at the bottom. Each sequence is identified by the strain number and the I-CeuI fragment from which it was isolated, except in the case of serovar Typhimurium, where the individual rrl gene is indicated. Letters in parentheses indicate the family of IVSs to which each sequence belongs, where a family consists of sequences with 90% or greater nucleotide identity based on DNASIS (see Tables ​Tables33 and ​and4).4). We propose four families for helix 25 and two families for helix 45. The species are as follows: Pv, Proteus vulgaris; Pp, Proteus penneri; Pm, Proteus mirabilis; Pr, Providencia rettgeri, and S. typhimurium, Salmonella serovar Typhimurium. Numbers at the end of each sequence indicate the base pairs in the IVS.

Journal:

Article Title: Fragmentation of 23S rRNA in Strains of Proteus and Providencia Results from Intervening Sequences in the rrn (rRNA) Genes

doi:

Figure Lengend Snippet: Intervening sequences from individual genes for rRNA of selected Proteus, Providencia, and Salmonella strains. Individual rrl genes were sequenced as described in Materials and Methods, and aligned using CLUSTAL X. The conserved residues are shown by dots, and deletions are shown by spaces. The consensus sequence is at the bottom. Each sequence is identified by the strain number and the I-CeuI fragment from which it was isolated, except in the case of serovar Typhimurium, where the individual rrl gene is indicated. Letters in parentheses indicate the family of IVSs to which each sequence belongs, where a family consists of sequences with 90% or greater nucleotide identity based on DNASIS (see Tables ​Tables33 and ​and4).4). We propose four families for helix 25 and two families for helix 45. The species are as follows: Pv, Proteus vulgaris; Pp, Proteus penneri; Pm, Proteus mirabilis; Pr, Providencia rettgeri, and S. typhimurium, Salmonella serovar Typhimurium. Numbers at the end of each sequence indicate the base pairs in the IVS.

Article Snippet: Lane 1, P. vulgaris (Pv, SGSC3360); lane 2, P. vulgaris (SA5474); lane 3, P. rettgeri (Pr, SA5473); lane 4, Proteus penneri (Pp, SA5462); lane 5, Proteus mirabilis (Pm, SA5450); lane 6, Morganella morganii (Mm, SA5438); lane 7, P. vulgaris (ATCC 13315, ATCC type strain); lane 8, P. vulgaris (ATCC 29905); lane 9, S. enterica serovar Typhimurium LT2 (Stm, SGSC1412); lane 10, E. coli K-12 (Ec, SA1332). (A) The regions of rrl genes containing IVSs were amplified by PCR, with primers P1 and P2 for helix 25 and primers P3 and P4 for helix 45 (as illustrated in Fig. ).

Techniques: Sequencing, Isolation