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D9893

Sigma-Aldrich

pBR322 Plasmid DNA from E. coli RRI

lyophilized powder

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1 UNIT
CN¥4,469.43
5 UNITS
CN¥17,897.47

CN¥4,469.43


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1 UNIT
CN¥4,469.43
5 UNITS
CN¥17,897.47

About This Item

CAS Number:
EC Number:
MDL number:
UNSPSC Code:
12352200
eCl@ss:
32160414
NACRES:
NA.52

CN¥4,469.43


Available to ship onApril 27, 2025Details

New, lower price on this item!

biological source

Escherichia coli

Quality Level

grade

Molecular Biology

form

lyophilized powder

mol wt

2.9 MDa
4363 bp

storage temp.

2-8°C

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This Item
D4904D3404D4154
mol wt

2.9 MDa, 4363 bp

mol wt

2.9 MDa, 4363 bp

mol wt

-

mol wt

-

form

lyophilized powder

form

buffered aqueous solution

form

buffered aqueous solution

form

buffered aqueous solution

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

grade

for molecular biology

grade

for molecular biology

grade

for molecular biology

grade

for molecular biology

biological source

Escherichia coli

biological source

-

biological source

-

biological source

Escherichia coli (RRI)

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

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).

Specificity

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.

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 as a low molecular weight DNA to test the enzymatic activity of partially purified component from Perna viridis (Linn.)[1] It has also been used for investigating its effect on the calcium carbonate particle morphology by scanning electron microscopy studies[2]

Biochem/physiol Actions

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.

Components

DNA is provided as a powder, lyophilized from a solution of 1 mM Tris-HCl (pH 7.5) with 1mM NaCl and 1mM EDTA.

Other Notes

Accession number: J01749
Accession number: J01749

related product

Product No.
Description
Pricing

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Changes in tumorigenesis- and angiogenesis-related gene transcript abundance profiles in ovarian cancer detected by tailored high density cDNA arrays.
Martoglio, A.-M., et al.
Cancer Biochemistry Biophysics, 6, 750-750 (2000)
S Iuliano et al.
Journal of chromatography. A, 972(1), 77-86 (2002-10-25)
A HPLC technique has been developed, based on hydrophobic-interaction Chromatography with a non-porous packing (TSKgel Butyl-NPR, Tosoh Biosep LLC), that allows separation of the open circular (nicked) and supercoiled forms of five DNA plasmids, ranging in size from 4 to
S Leah Etheridge et al.
PLoS genetics, 4(11), e1000259-e1000259 (2008-11-15)
Dishevelled (Dvl) proteins are important signaling components of both the canonical beta-catenin/Wnt pathway, which controls cell proliferation and patterning, and the planar cell polarity (PCP) pathway, which coordinates cell polarity within a sheet of cells and also directs convergent extension
Muhammed Zafar A N Iqbal et al.
Indian journal of experimental biology, 54(12), 816-821 (2016-12-01)
Viral diseases are not only responsible for health related issues but also exert pressure on the State economy. Tropical and subtropical countries have more prevalence of virus associated pathological conditions such as chickenpox, adenovirus related infections, dengue, chickengunya, infectious mononucleosis
Bei Cheng et al.
Journal of colloid and interface science, 352(1), 43-49 (2010-09-11)
Calcium carbonate microspheres with different surface structures were successfully prepared by the reaction of sodium carbonate with calcium chloride in the presence of deoxyribonucleic acid (DNA) at room temperature. The as-prepared products were characterized by scanning electron microscopy (SEM), transmission

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