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MilliporeSigma

D3812

DirectLoad 50 bp DNA Step Ladder

ready-to-use marker for DNA electrophoresis

Synonyme(s) :

DirectLoad 50 bp DNA Marker, Ready-to-use 50 bp DNA Marker, Ready-to-use DirectLoad 50 bp DNA Marker, Ready-to-use DirectLoad 50 bp DNA Step Ladder

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A propos de cet article

NACRES:
NA.25
UNSPSC Code:
41105335
Service technique
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Quality Level

form

(liquid)

usage

sufficient for 100 loads

suitability

suitable for electrophoresis (DNA)

storage temp.

−20°C

General description

Sigma′s DirectLoad 50 bp DNA Step Ladder contains 17 blunt-ended fragments consisting of 50 bp repeats from 50 to 500 bp, 100 bp repeats from 600 to 900 bp, and 1 kb repeats from 1 to 3 kb. Ten ul of the ladder can be loaded directly in a single lane on an agarose or polyacrylamide gel.

Application

Suitable for size determination of PCR-generated DNA fragments with either agarose or polyacrylamide gels.
DirectLoad 50 bp DNA Step Ladder has been used for cell lysis and genomic cleavage detection assay.

Features and Benefits

  • Ready-to-load
  • Easy-to-use
  • Popular band sizes

Other Notes

For optimal resolution, the recommended agarose gel concentration is 2.0%.
Sigma′s DirectLoad 50 bp DNA Step Ladder is provided in a gel-loading solution of 5% glycerol, 4.2 mM EDTA, 0.083% orange G and 0.0125% xylene cyanol.

Legal Information

DirectLoad is a trademark of Sigma-Aldrich Co. LLC


wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Classe de stockage

12 - Non Combustible Liquids



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Protocoles

JumpStart™ Taq DNA Polymerase is an antibody-inactivated, hot start enzyme.

Protocol using antibody mediated hot start polymerase. Method has short activation period (<1min), and results in higher yields and more specificity over standard PCR methods.

Articles

Markers for gel electrophoresis aid size determination of DNA, PCR fragments, and RNA, staining well with common nucleic acid stains.

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.

Contenu apparenté


Solid-phase reverse transfection for intracellular delivery of functionally active proteins
Bulkescher R, et al.
Genome Research, 27(10), 1752-1758 (2017)
Cinzia Fabbro et al.
FEMS microbiology letters, 307(2), 158-164 (2010-04-24)
Culturable vibrios were isolated from seawater collected during an annual sampling study performed along the Gulf of Trieste coast (Northern Adriatic Sea), and conventional culturing and identification methods were used to investigate the presence of Vibrio parahaemolyticus. Biochemically selected Vibrio



Numéro d'article de commerce international

RéférenceGTIN
D3812-1VL04061835515967