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Roche

DIG Easy Hyb

greener alternative

suitable for hybridization, solution

Synonym(s):

DIG system

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About This Item

UNSPSC Code:
41105326

form

solution

Quality Level

packaging

pkg of 500 mL

manufacturer/tradename

Roche

greener alternative product characteristics

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

sustainability

Greener Alternative Product

technique(s)

hybridization: suitable

greener alternative category

storage temp.

2-8°C

General description

DIG Easy Hyb is a nontoxic, ready-to-use hybridization buffer. DIG Easy Hyb does not contain formamide, but facilitates lowering of hybridization temperature comparable to buffers that contain 50% formamide.
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 using 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.

Application

DIG Easy Hyb can be used in all membrane hybridization applications using nonradioactive (e.g., digoxigenin-labeled) nucleic acid probes. DIG Easy Hyb is ready-made, and can be used without any additions. It is specifically designed for use with DIG kits.

Quality

Absence of contaminants: DNase- and RNase-free.

Other Notes

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

Legal Information

DIG Easy Hyb is a trademark of Roche

also commonly purchased with this product

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 2

flash_point_f

No data available

flash_point_c

No data available


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Human cytomegalovirus infection contributes to glioma disease progression via up-regulating endocan expression
Xing Yang
Translational Research (2016)
Hugo V Miranda et al.
Molecular & cellular proteomics : MCP, 13(1), 220-239 (2013-10-08)
SAMP1 and SAMP2 are ubiquitin-like proteins that function as protein modifiers and are required for the production of sulfur-containing biomolecules in the archaeon Haloferax volcanii. Here we report a novel small archaeal modifier protein (named SAMP3) with a β-grasp fold
Borhan Uddin et al.
BMC genomics, 16, 1082-1082 (2015-12-23)
Highly efficient genome editing can be achieved through targeting an endonuclease to specific locus of interest. Engineered zinc-finger nuclease (ZFN) and CRISPR-associated protein-9 nuclease (Cas9) offer such an elegant approach for genome editing in vertebrate cells. In this study, we
Samuel Vega-Estévez et al.
mBio, 12(5), e0187121-e0187121 (2021-09-08)
Microorganisms need to adapt to environmental changes, and genome plasticity can lead to rapid adaptation to hostile environments by increasing genetic diversity. Here, we investigate genome plasticity in the CTG(Ser1) yeast Scheffersomyces stipitis, an organism with an enormous potential for
Fang Liu et al.
International journal of molecular sciences, 22(22) (2021-11-28)
It is vital to develop high-throughput methods to determine transgene copy numbers initially and zygosity during subsequent breeding. In this study, the target sequence of the previously reported endogenous reference gene hmg was analyzed using 633 maize inbred lines, and

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