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Merck

R7020

Transcript RNA Markers 0.2-10 kb

for RNA electrophoresis

Synonym(s):

RNA agarose gel electrophoresis ladder, RNA agarose gel electrophoresis marker, northern blot ladder, northern blot marker, ssRNA ladder, ssRNA marker, tRNA ladder, tRNA marker

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50 μG

€175.00

€175.00


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About This Item

UNSPSC Code:
41105337
NACRES:
NA.25

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grade

Molecular Biology

Quality Level

form

liquid

usage

25 uses

solubility

water: soluble

suitability

suitable for electrophoresis (RNA)

storage temp.

−70°C

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This Item
R7644P9577D7058
grade

for molecular biology

grade

for molecular biology

grade

-

grade

-

Quality Level

300

Quality Level

200

Quality Level

200

Quality Level

100

form

liquid

form

liquid

form

liquid

form

liquid

storage temp.

−70°C

storage temp.

−70°C

storage temp.

−20°C

storage temp.

−20°C

usage

25 uses

usage

25 uses

usage

sufficient for 50 uses

usage

100 uses

suitability

suitable for electrophoresis (RNA)

suitability

suitable for electrophoresis (RNA)

suitability

suitable for electrophoresis (DNA)

suitability

suitable for electrophoresis (DNA)

General description

Sigma′s Transcript RNA Marker (0.2 – 10 kb) contains 9 RNA transcripts from 200 – 10,000 bases. Two ul of the ladder should be diluted in gel loading buffer and then loaded in a single lane on an agarose gel.

Application

Suitable for size determination of small RNA using native or denaturing agarose gel electrophoresis.
Transcript RNA Markers 0.2-10 kb has been used as a molecular weight marker for northern blot hybridization.[1]

Other Notes

Contains nine defined RNA transcripts, 200–10,000 nucleotides
For optimal resolution, the recommended agarose gel concentration is 1.0%.
Sigma′s Transcript RNA Marker (0.2 – 10 kb) is provided in a gel-loading solution with 10 mM Tris-HCl (pH 8.0), with 1.0 mM EDTA.

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Barley lesion mimics, supersusceptible or highly resistant to leaf rust and net blotch.
Wright SA, et al.
Plant Pathology, 62, 982-992 (2013)
Magda Dudek et al.
Nucleic acids research, 48(14), 7786-7800 (2020-06-26)
Marine flavobacteria possess dedicated Polysaccharide Utilization Loci (PULs) enabling efficient degradation of a variety of algal polysaccharides. The expression of these PULs is tightly controlled by the presence of the substrate, yet details on the regulatory mechanisms are still lacking.

Articles

Choose the appropriate markers and ladders for nucleic acid size determination of samples separated by electrophoresis. Determine size of DNA, RNA and PCR-generated fragments using agarose or polyacrylamide gels.

Protocols

Learn Northern and Southern blotting basics, with protocols and applications for macromolecule transfer to membrane supports.

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Questions

1–2 of 2 Questions  
  1. in what proportion should i mix RNA marker and loading dye buffer.

    1 answer
    1. RNA Marker sample solutions for electrophoresis should be prepared as follows: Mix 2-4 µl of RNA Marker, add water (Rnase free) to make up to 5 µl, then add 3 µl of RNA Sample Loading Buffer, and 1 µl of 200 mM Potassium Acetate, pH 4.5. Additional information can be found in the Product Information Sheet.

      Helpful?

  2. Can I denaturate it using Glyoxal?

    1 answer
    1. This product has been tested on 1% agarose gel with formaldehyde. It has not been specifically qualified for use with glyoxal, however there is no reason to suspect that it would not be suitable. See the reference in the link below comparing formaldehyde to glyoxal:
      https://link.springer.com/protocol/10.1385/0-89603-127-6:1

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