PCR Sizer 100 bp DNA Ladder
Ideal for PCR product size confirmation
For research use only and NOT intended for in vitro diagnostics.
PCR Sizer 100 bp DNA Ladder
Ideal for PCR product size confirmation
$75.00
SKU
11400
Register today to receive an exclusive 15% off* on your first order.
Features and Benefits
- Ready-to-use
- Quantitative
- Highly Stable
- Precise
- Ten discrete fragments from 100 bp to 1000 bp
- Higher intensity reference band at 500 bp
The Norgen PCRSizer 100 bp DNA Ladder is prepared to ensure quality and batch-to-batch consistency. Our PCRSizer contains ten discrete fragments ranging from 100 bp to 1000 bp in 100 bp increments with a higher intensity reference band at 500 bp. This Ladder is ideal for PCR product size confirmation.
Contents:
1mL of premixed DNA ladder (0.5µg/10µL) in loading buffer (10mM EDTA, 10% glycerol, 0.015% bromophenol blue, and 0.17% SDS).
Details
Supporting Data
PCR Sizer 100 bp DNA Ladder (Cat# 11400) - 100 loads
Ladder Properties:
• Ten discrete bands, ranging from 100 bp to 1,000 bp
• Higher intensity band at 500 bp for easy reference
• Ten discrete bands, ranging from 100 bp to 1,000 bp
• Higher intensity band at 500 bp for easy reference
Fragment
|
Size (bp)
|
Mass (ng)
|
1
|
1000
|
78
|
2
|
900
|
70
|
3
|
800
|
62
|
4
|
700
|
55
|
5
|
600
|
47
|
6
|
500
|
78
|
7
|
400
|
31
|
8
|
300
|
24
|
9
|
200
|
31
|
10
|
100
|
24
|
Recommended Use:
Mix thoroughly. For best results, load 10µL of DNA ladder per well. For precise mass determination with a densitometer, stain gel after electrophoresis using 0.5µg/mL ethidium bromide for 30-40 minutes. The table above shows the size and mass for each band based on 10µL ladder per well.
Storage:
Stable at room temperature. For longer term storage, -20°C is recommended.
This ladder was standardized using 10µL of DNA per lane on a 0.8 cm thick, 13 x 15 cm, 1.0% agarose gel run in TAE buffer.
Documentation
Citations
Title | Genetic diversity in the germplasm of tropical maize landraces determined using molecular markers |
Citation | Genetics and Molecular Research 2013. |
Authors | D Molin, CJ Coelho, DS Maximo, FS Ferreira, JR Gardingo, RR Matiello |