D4904
pBR322 Plasmid DNA from E. coli RRI
buffered aqueous solution
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Informacje o tej pozycji
Numer CAS:
UNSPSC Code:
12352200
eCl@ss:
32160414
EC Number:
297-227-2
NACRES:
NA.51
MDL number:
Origin of replication:
BR322
Przejdź do
Pomoc techniczna
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Pozwól nam pomócrecombinant
expressed in E. coli
grade
Molecular Biology
form
buffered aqueous solution
mol wt
2.9 MDa, 4363 bp
origin of replication
BR322
selection
ampicillin
shipped in
dry ice
storage temp.
−20°C
Quality Level
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Ta pozycja | |||
|---|---|---|---|
| origin of replication BR322 | origin of replication - | origin of replication - | origin of replication - |
| mol wt 2.9 MDa, 4363 bp | mol wt 2.9 MDa, 4363 bp | mol wt - | mol wt - |
| form buffered aqueous solution | form lyophilized powder | form buffered aqueous solution | form buffered aqueous solution |
| recombinant expressed in E. coli | recombinant - | recombinant - | recombinant - |
| grade for molecular biology | grade for molecular biology | grade for molecular biology | grade for molecular biology |
| shipped in dry ice | shipped in - | shipped in dry ice | shipped in dry ice |
General description
Plasmid pBR322 was one of the first multipurpose cloning vectors constructed for use in E. coli. This plasmid is derived from the ColE1-type plasmid pMB1 and shares the same type of replication mechanism and controls as ColE1 and relatives. Plasmid pBR322 confers resistance to ampicillin and tetracycline. The plasmid sequence has been published.
The plasmid has unique restriction sites within the gene for ampicillin resistance (Pst I, Pvu I, and Sca I), within the gene for tetracycline resistance (BamH I, BspM I, EcoR V, Nhe I, Nru I, Sal I, Sph I, and Xma III), and elsewhere (Aat II, Ava I, Bal I, Bsm I, BspM II, Cla I, EcoR I, Hind III, Nde I, Pvu II, Ssp I, Sty I, and Tth111 I).
The plasmid has unique restriction sites within the gene for ampicillin resistance (Pst I, Pvu I, and Sca I), within the gene for tetracycline resistance (BamH I, BspM I, EcoR V, Nhe I, Nru I, Sal I, Sph I, and Xma III), and elsewhere (Aat II, Ava I, Bal I, Bsm I, BspM II, Cla I, EcoR I, Hind III, Nde I, Pvu II, Ssp I, Sty I, and Tth111 I).
Application
Plasmid pBR322 was one of the first multipurpose cloning vectors constructed for use in Escherichia coli. This plasmid and derivatives have been used for a number of purposes including cloning, selection and expression of recombinant molecules, construction of shuttle vectors and vectors for nucleotide sequencing, studies of elements involved in gene expression, as plasmid DNA standards, and as a model system for studies on prokaryotic plasmid replication.
pBR322 Plasmid DNA from E. coli RRI has been used to study about ferrous ion-induced strand breaks in the plasmid pBR322 are mediated through hydrogen peroxide.[1]
Biochem/physiol Actions
Unique Sites: Within the gene for ampicillin resistance: Pst I, Pvu I, Sca I; Within the gene for tetracycline resistance: BamH I, BspM I, EcoR V, Nhe I, Nru I, Sal I, Sph I, Xma III; other unique sites: Aat II, Ava I, Bal I, Bsm I, BspM II, Cla I, EcoR I, Hind III, Nde I, Pvu II, Ssp I, Sty I, Tth111 I.
One of the most commonly used cloning vectors, pBR322, confers resistance to ampicillin and tetracycline. The DNA sequence of the entire plasmid has been published.
This plasmid is derived from the ColE1-type plasmid pMB1 and shares the same type of replication mechanism and controls as ColE1 and relatives.
Other Notes
Accession number: J01749
DNA is provided in a solution of 10 mM Tris-HCl (pH 8.0) with 1 mM EDTA.
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Numer produktu
Opis
Cennik
Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Jörg Flemmig et al.
European biophysics journal : EBJ, 36(4-5), 377-384 (2006-10-19)
Ferrous ion-induced generation of single and multiple strand breaks in the DNA plasmid pBR322 induces the formation of two new plasmid forms with altered electrophoretic mobility. The yield of these plasmid forms, the circular relaxed and the linear forms, depended
Ferrous ion-induced strand breaks in the DNA plasmid pBR322 are not mediated by hydrogen peroxide
Flemmig J and Arnhold J
European Biophysics Journal, 36(4-5), 377-384 (2007)
Charles J Addison et al.
BioTechniques, 37(3), 376-378 (2004-10-09)
Transformation of Escherichia coli plays an important role in recombinant DNA technology. Most current transformation protocols require that the cells be treated to attain a particular physiological state known as "competence," and this makes transformation procedures lengthy and arduous. Here
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