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Merck

11585614910

Roche

Zestaw startowy DIG-High Prime do znakowania i detekcji DNA II

greener alternative

sufficient for 12 labeling reactions (10 ng to 3 μg per assay), sufficient for 24 blots (blots of 100 cm2)

Synonim(y):

System DIG, znakowanie DNA

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Wybierz wielkość

12 REACTIONS

2920,00 zł

2920,00 zł


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Informacje o tej pozycji

Kod UNSPSC:
41105500
NACRES:
NA.54

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zastosowanie

sufficient for 12 labeling reactions (10 ng to 3 μg per assay)
sufficient for 24 blots (blots of 100 cm2)

Poziom jakości

producent / nazwa handlowa

Roche

charakterystyka ekologicznej alternatywy

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

kategoria ekologicznej alternatywy

temp. przechowywania

−20°C

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Ta pozycja
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usage

sufficient for 12 labeling reactions (10 ng to 3 μg per assay), sufficient for 24 blots (blots of 100 cm2)

usage

sufficient for 12 labeling reactions, sufficient for 24 blots

usage

sufficient for 25 labeling reactions, sufficient for 50 blots

usage

sufficient for 40 labeling reactions

manufacturer/tradename

Roche

manufacturer/tradename

Roche

manufacturer/tradename

Roche

manufacturer/tradename

Roche

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

sustainability

Greener Alternative Product

sustainability

Greener Alternative Product

sustainability

Greener Alternative Product

greener alternative category

Aligned,

greener alternative category

, Aligned

greener alternative category

, Aligned

greener alternative category

, Aligned

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Opis ogólny

DIG-High Prime DNA Labeling and Detection Starter Kit II is a convenient kit for random-primed labeling of DNA templates with digoxigenin (DIG)-11- deoxyuridine triphosphate (dUTP), alkali-labile and chemiluminescent detection of the DIG-labeled hybrids. This kit was assembled with convenience in mind, offering ready-to-use CSPD supplied with a dripping device for easy application, ready-made blocking solution, and DIG Easy Hyb granules. The DIG-High Prime mixture includes stabilized Klenow enzyme, nucleotides, primers and reaction buffer, all in one convenient reagent.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is designed as a safer chemical.  The DIG System was established as a sensitive and cost-effective alternative to radioactivity for the labeling and detection of nucleic acids. There are many available publications that prove the versatility of the DIG System, so use of radio-labeling is no longer the only option for labeling of DNA for hybridization.

Zastosowanie

DIG-High Prime DNA Labeling and Detection Starter Kit II has been used in a variety of hybridization techniques:
  • in Southern blots[1]
  • in northern blots[2]
  • in dot blots[3]
  • in colony and plaque hybridizations
  • for all types of filter hybridization
  • for single-copy gene detection in total genomic DNA, even from organisms with high complexity, for example, human, barley, and wheat

Działania biochem./fizjol.

The DIG High Prime DNA Labeling and Detection Starter Kit II uses digoxigenin (DIG), a steroid hapten, to label DNA probes for hybridization and subsequent chemiluminescence detection by enzyme immunoassay. The "random primed" DNA labeling method originally developed by Feinberg and Vogelstein is based on the hybridization of oligonucleotides of all possible sequences to the denatured DNA to be labeled. The input DNA serves solely as a template for the synthesis of labeled DNA, and is not degraded during the reaction, making it possible to label minimal amounts of DNA (10 ng) with this method.The complementary DNA strand is synthesized by Klenow polymerase using the 3′-OH termini of the random oligonucleotides as primers. Modified deoxyribonucleoside triphosphates, labeled with digoxigenin present in the reaction, are incorporated into the newly synthesized complementary DNA strand.

Opakowanie

1 kit containing 7 components.

Inne uwagi

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

Numer produktu
Opis

  • DIG-High Prime 5x concentrated

  • DIG-labeled Control DNA, pBR328 (linearized with Bam HI) 5 μg/ml

  • DNA Dilution Buffer

  • Anti-Digoxigenin-AP Conjugate antibody

  • CSPD ready-to-use

  • Blocking Solution 10x concentrated

  • DIG Easy Hyb Granules

Piktogramy

Exclamation mark

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

Eye Irrit. 2 - Skin Irrit. 2

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

does not flash

Temperatura zapłonu (°C)

does not flash


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Eva-Maria Holstein et al.
Cell reports, 7(4), 1259-1269 (2014-05-20)
A large and diverse set of proteins, including CST complex, nonsense mediated decay (NMD), and DNA damage response (DDR) proteins, play important roles at the telomere in mammals and yeast. Here, we report that NMD, like the DDR, affects single-stranded
Erum Dilshad et al.
PloS one, 10(10), e0140266-e0140266 (2015-10-09)
The potent antimalarial drug artemisinin has a high cost, since its only viable source to date is Artemisia annua (0.01-0.8% DW). There is therefore an urgent need to design new strategies to increase its production or to find alternative sources.
Emmanuel Ogwok et al.
Journal of virological methods, 169(2), 296-304 (2010-08-10)
Cassava brown streak disease (CBSD), caused by two distinct species, Cassava brown streak Uganda virus (CBSUV) and Cassava brown streak virus (CBSV), is a major constraint to cassava (Manihot esculenta Crantz) production in Africa. Absence of infectious clones of CBSUV
Ling Zhang et al.
International journal of genomics, 2014, 921950-921950 (2014-09-10)
The Delta-12 oleate desaturase gene (FAD2-1), which converts oleic acid into linoleic acid, is the key enzyme determining the fatty acid composition of seed oil. In this study, we inhibited the expression of endogenous Delta-12 oleate desaturase GmFad2-1b gene by
Rajiv R Mohan et al.
PloS one, 6(4), e18771-e18771 (2011-05-03)
Untargeted and uncontrolled gene delivery is a major cause of gene therapy failure. This study aimed to define efficient and safe tissue-selective targeted gene therapy approaches for delivering genes into keratocytes of the cornea in vivo using a normal or

Produkty

Digoxigenin (DIG) labeling methods and kits for DNA and RNA DIG probes, random primed DNA labeling, nick translation labeling, 5’ and 3’ oligonucleotide end-labeling.

Metody znakowania digoksygeniną (DIG) i zestawy do sond DNA i RNA DIG, znakowanie DNA z losowym primerem, znakowanie nickiem translacyjnym, znakowanie końcowe oligonukleotydów 5' i 3'.

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