11585614910

DIG-High Prime DNA Labeling and Detection Starter Kit II

Manufacturer: Sigma Aldrich

Synonym(S): DIG system, dna labeling

Select a Size

Pack Size SKU Availability Price
12 REACTIONS 11585614910-12-REACTIONS In Stock ₹ 60,417.30

11585614910 - 12 REACTIONS

₹ 60,417.30

In Stock

Quantity

1

Base Price: ₹ 60,417.30

GST (18%): ₹ 10,875.114

Total Price: ₹ 71,292.414

usage

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

Quality Level

100

manufacturer/tradename

Roche

greener alternative product characteristics

Designing Safer ChemicalsLearn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

greener alternative category

Aligned,

storage temp.

−20°C

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Description

  • General description: 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.
  • Application: 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 hybridizationsfor all types of filter hybridizationfor single-copy gene detection in total genomic DNA, even from organisms with high complexity, for example, human, barley, and wheat
  • Packaging: 1 kit containing 7 components.
  • Principle: 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.
  • Other Notes: For life science research only. Not for use in diagnostic procedures.

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Precautionary Statements

P264 - P280 - P302 + P352 - P332 + P313 - P337 + P313 - P362 + P364

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

Flash Point(F)

does not flash

Flash Point(C)

does not flash

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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)

Quality Level:
100

manufacturer/tradename:
Roche

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Designing Safer ChemicalsLearn more about the Principles of Green Chemistry.

sustainability:
Greener Alternative Product

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storage temp.:
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100

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Roche

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100

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Roche

greener alternative product characteristics:
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