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P1473

PCR 100 bp Low Ladder

for electrophoresis of PCR fragments

Sinónimos:

100bp maker, 100bp marker for agarose gel electrophoresis, 100pb ladder for agarose gel electrophoresis, DNA ladder, DNA marker, gel ladder, gel marker

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NACRES:
NA.25
UNSPSC Code:
41141827
Biological source:
synthetic
Form:
liquid
Storage temp.:
−20°C
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biological source

synthetic

Quality Level

grade

Molecular Biology

form

liquid

usage

75 uses

suitability

suitable for electrophoresis (DNA)

storage temp.

−20°C

General description

Sigma′s PCR 100 bp Low Marker contains 10 dsDNA fragments from 100 – 1,000 bases, evenly spaced in 100 bp repeats. Two ul of the ladder should be diluted in gel loading buffer and then loaded in a single lane on an agarose gel.
The PCR 100 bp low ladder has been specially designed for the size determination of polymerase chain reaction (PCR) generated DNA fragments.

Application

PCR 100 bp Low Ladder has been used:
  • in agarose gel electrophoresis as a standard DNA marker to obtain DNA fragments of about 240 bp for polymerase chain reaction (PCR)-denaturing gradient gel electrophoresis (DGGE) analysis[1]
  • to visualize DNA from enzyme digested PCR mixture
  • to estimate the molecular weight of the PCR product fragments

Other Notes

Contains 10 bands, 100–1,000 bp in exact 100 bp spaced (ladder) recombinant repeats.
For optimal resolution, the recommended agarose gel concentration is 2.0%.
Sigma′s PCR 100 bp Low Marker is provided in a solution of 10 mM Tris-HCl (pH 8.0), with 1.0 mM EDTA.

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Este artículo
D3687P9577P1598
grade

Molecular Biology

grade

Molecular Biology

grade

-

grade

Molecular Biology

biological source

synthetic

biological source

-

biological source

-

biological source

fermentation/recombinant (E. coli strain DH5A)

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

100

form

liquid

form

liquid

form

liquid

form

liquid

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

2-8°C

usage

75 uses

usage

75 uses

usage

sufficient for 50 uses

usage

80 uses


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Clase de almacenamiento

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flash_point_f

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flash_point_c

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Frontiers in microbiology, 3, 436-436 (2013-01-15)
In this study, bacterial composition of iru produced by natural, uncontrolled fermentation of Parkia biglobosa seeds was assessed using culture-independent method in combination with culture-based genotypic typing techniques. PCR-denaturing gradient gel electrophoresis (DGGE) revealed similarity in DNA fragments with the
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SKUGTIN
P1473-1VL04061835516230
P1473-25UG04061831598148

Questions

  1. What loading buffer/dye is the P1473 DNA ladder compatible with for loading onto a gel.

    1 answer
    1. This DNA ladder can be used with a loading buffer such as G2526:
      https://www.sigmaaldrich.com/product/sigma/g2526

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