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Merck

HPPIKRO

Roche

High Pure Plasmid Isolation Kit

Roche, pkg of 50 purifications (11754777001), pkg of 250 purifications (11754785001)

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
41105500

gyártó/kereskedő neve

Roche

Minőségi szint

kiszerelés

pkg of 250 purifications (11754785001)
pkg of 50 purifications (11754777001)

Általános leírás

Low to medium throughput, mini scale, plasmid isolation.

The High Pure Plasmid Isolation Kit isolates purified plasmid DNA in small quantities using the alkaline lysis method, a commonly used method that generates highly purified plasmid DNA from E. coli, free of RNA contamination.
Nucleic acids bind to the surface of the glass fiber fleece in the presence of a chaotropic salt (guanidine HCl). This allows the High Pure filter tube to specifically immobilize nucleic acids (both DNA and RNA) while they are freed of contaminants.

Capacity: The High Pure Spin Filter Tubes hold up to 700 μL sample volume.
Sample: 0.5 - 4.0 mL cultures of E. coli (harvested at a density of 1.5 - 5.0 A 600 units/mL)

Alkalmazás

The High Pure Plasmid Isolation Kit prepares up to 15 μg purified plasmid DNA from bacterial cultures, that can be used directly in most molecular biology applications:
  • PCR
  • Sequencing
  • Cloning
  • In vitro transcription
  • Restriction enzyme digests
  • Random primed labeling

Tulajdonságok és előnyök

  • Quickly purify up to 24 plasmid samples in <30 minutes.
  • Minimize DNA loss with a kit that removes contaminants without precipitation or other handling steps that degrade DNA.
  • Improve reliability and reproducibility in downstream applications with a kit that removes RNA and other impurities that cause plasmid DNA to behave unpredictably.
  • Eliminate the use of hazardous organic compounds such as cesium chloride, phenol, chloroform, and ethidium bromide.

Komponensek

  • Suspension Buffer
  • RNase A, dry powder
  • Lysis Buffer
  • Binding Buffer
  • Wash Buffer I
  • Wash Buffer II
  • Elution Buffer
  • High Pure Spin Filter Tubes (containing glass fiber fleece)
  • Collection Tubes

Minőség

Plasmid pUC19 (4.5 μg) is purified from a 1.5 mL suspension of E. coli JM83, which was grown in LB-medium with ampicillin for 16 hours, to a cell density of 5 A 600 units/mL. 1 μg of the purified plasmid DNA is incubated for 1 hour at +37°C with 5 units of the restriction endonuclease Eco RI and then analyzed by agarose gel electrophoresis. The isolated plasmid DNA is as sensitive to restriction endonuclease digestion as plasmid DNA isolated by CsCl density centrifugation.

Elkészítési megjegyzés

The kit relies on alkaline lysis to release plasmid DNA from bacteria. RNase removes all RNA in the lysate. After cellular debris and (entrapped) genomic DNA are removed by centrifugation, the remaining supernatant is mixed with a chaotropic salt and applied to the glass fiber fleece in a High Pure Spin Filter Tube. Under the buffer conditions used in the procedure, the plasmid binds to the glass fiber fleece, while contaminating substances (salts, proteins, and other cellular contaminants) do not. Brief wash-and-spin steps readily remove these contaminants. Once purified, the plasmid can be easily eluted in a small volume of low-salt buffer or water.

Egyéb megjegyzések

For life science research only. Not for use in diagnostic procedures.

Piktogramok

CorrosionExclamation mark

Figyelmeztetés

Danger

Figyelmeztető mondatok

Veszélyességi osztályok

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1

Tárolási osztály kódja

8B - Non-combustible, corrosive hazardous materials

WGK

WGK 1

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable


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Analitikai tanúsítványok (COA)

Lot/Batch Number

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Dokumentumtár megtekintése

Chromosome evolution in Solanum traced by cross-species BAC-FISH.
Szinay D, et al.
The New phytologist, 195(3), 688-698 (2012)
Function Based Metagenomics Approach for Obtaining Lipase from Acid Mine Drainage Site.
Tutuncu H E, et al.
International Journal Series in Engineering Science, 1-20 (2017)
Marc Quirynen et al.
Journal of clinical periodontology, 38(6), 581-589 (2011-04-15)
Recent studies showed that qPCR could detect bacteria related to periodontitis and peri-implantitis in a low concentration after full-mouth tooth extraction. This study monitored the microbiota from tooth extraction, over 9 months of full edentulism, up to 1 year after
Molecular, cytological, and immunocytochemical study and kDNA
sequencing of laryngeal Leishmania infantum infectionv
Oryan A, et al.
Parasitology Research, 112(4), 1799-1804 (2013)

Protocols

Determine the labeling efficiency in terms of μg (expected yield of a standard labeling reaction is 20 μg of DIG labeled RNA per μg linearized template DNA after the DIG RNA labeling reaction).

Tudóscsoportunk valamennyi kutatási területen rendelkezik tapasztalattal, beleértve az élettudományt, az anyagtudományt, a kémiai szintézist, a kromatográfiát, az analitikát és még sok más területet.

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