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11373099910

Roche

RNA Molecular Weight Marker III, DIG-labeled

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About This Item

UNSPSC Code:
41105335

form

solution

packaging

pkg of 200 μL (2 μg)

manufacturer/tradename

Roche

concentration

10 ng/μL

shipped in

dry ice

storage temp.

−20°C

General description

The fragments are prepared by in vitro transcription of linearized plasmids with SP6 or T7 RNA Polymerase in separate reactions. The transcripts are then combined at a ratio that gives bands of uniform intensity when separated by gel electrophoresis.
The transcripts are labeled in a photodigoxigenin reaction so that a digoxigenin moiety is present every 200th to 300th nucleotide.
Size Range: 0.3 to 1.5 kb

Application

RNA molecular weight marker III, DIG-labeled has been used in RNA electrophoresis and northern blot analysis.[1][2]

Sequence

Five fragments: 310, 438, 575, 1049, and 1517 bases.

Preparation Note

Working concentration: Transfer 40 to 100 ng of labeled RNA Molecular Weight Marker I per lane or 20 to 50 ng of RNA Molecular Weight Marker II or III per lane, depending on the reaction time in the detection step, to produce clear banding patterns.
Note: Taking the lane (slot) size of the agarose gel into account, load 100 ng for RNA marker I and 50 ng for RNA marker II or III.

Other Notes

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

Storage Class

12 - Non Combustible Liquids

wgk_germany

nwg

flash_point_f

No data available

flash_point_c

No data available


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Detection of Long Non-coding RNA Expression by Non-radioactive Northern Blots
Hu X, et al.
Methods in Molecular Biology, 177-188 (2016)
Tethering of Poly(A)-binding Protein Interferes with Non-translated mRNA Decay from the 5? End in Yeast
Tsuboi T, et al.
The Journal of Biological Chemistry, 285(44), 33589-33601 (2010)
Tatsuhisa Tsuboi et al.
The Journal of biological chemistry, 285(44), 33589-33601 (2010-08-25)
The decay of eukaryotic mRNA is triggered mainly by deadenylation, which leads to decapping and degradation from the 5' end of an mRNA. Poly(A)-binding protein has been proposed to inhibit the decapping process and to stabilize mRNA by blocking the

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