Nineteen discrete fragments ranging from 100 bp to 10000 bp
Higher intensity reference bands at 500 bp, 1000 bp and 5000 bp
The Norgen HighRangerPlus 100 bp DNA Ladder is prepared to ensure quality and batch-to-batch consistency. Our HighRangerPlus contains nineteen discrete fragments ranging from 100 bp to 10000 bp with higher intensity reference bands at 500 bp, 1000 bp and 5000 bp. This Ladder is ideal for size determination of digested DNA.
Contents: 1mL of premixed DNA ladder (0.5µg/10µL) in loading buffer (10mM EDTA, 10% glycerol, 0.015% bromophenol blue, and 0.17% SDS).
HighRanger Plus 100 bp DNA Ladder (Cat# 12000) – 100 loads
Ladder Properties:
Nineteen discrete fragments ranging from 100 bp to 10000 bp
Higher intensity bands at 500 bp, 1000 bp and 5000 bp for easy reference
Fragment
Size (bp)
Mass (ng)
1
10000
42
2
8000
33
3
6000
25
4
5000
42
5
4000
35
6
3000
27
7
2500
22
8
2000
18
9
1500
13
10
1000
40
11
900
28
12
800
25
13
700
34
14
600
19
15
500
44
16
400
13
17
300
18
18
200
13
19
100
10
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: This kit is stable for 2 years after the date of shipment.
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.
Other Products
IST-125 QuickSeal MicroTM Self Adhesive Sealing Film
Product Info
Document
Product Info
Overview
Low strength adhesive film that is transparent, peelable and suitable for short term storage.
This transparent polyester-based film has a low strength adhesive
It is designed as a low-cost sealing option, and useful for temporary storage and as a cover for applications such as centrifugation
End tabs allow for easy application and removal
This seal is removable without leaving residue on the plate
For all adhesive seals, the best sealing results are achieved using our Hand Roller or KAPS 500 Auto Sealer
Document
Low strength adhesive film that is transparent, peelable and suitable for short term storage.
Opentrons OT-2 Tips, 20µL. Optimized for volumes 1µL to 20µL. Clear Tips, Polypropylene. These tips are DNAse/RNAse, pyrogen and protease free – they are sterilized from ebeam irradiation. Not autoclavable.
Compatible with: Opentrons 8-Channel GEN2 P20 Electronic Pipettes, Opentrons Single-Channel GEN2 P20 Electronic Pipettes, Opentrons Single-Channel GEN1 P10 Electronic Pipettes, Opentrons 8-Channel GEN1 P10 Electronic PipettesOpentrons platform and workstation accuracy and precision performance is not validated with use of non-Opentrons tips.
Document
Opentrons OT-2 Tips, 20µL. Optimized for volumes 1µL to 20µL. Clear Tips, Polypropylene. These tips are DNAse/RNAse, pyrogen and protease free – they are sterilized from ebeam irradiation. Not autoclavable.
Compatible with: Opentrons 8-Channel GEN2 P20 Electronic Pipettes, Opentrons Single-Channel GEN2 P20 Electronic Pipettes, Opentrons Single-Channel GEN1 P10 Electronic Pipettes, Opentrons 8-Channel GEN1 P10 Electronic PipettesOpentrons platform and workstation accuracy and precision performance is not validated with use of non-Opentrons tips.
The MagPure Plasmid purification system uses the paramagnetic bead technology for high-throughput preparation of high-copy or low-copy plasmid DNA from E. coli cells. This kit also can be used with fosmid and BAC vector-based constructs. The system uses alkaline lysis followed by a MagPure purification to differentially bind plasmid DNA to paramagnetic beads. While the DNA is bound to the beads, contaminants can be rinsed away using a simple washing procedure. Because MagPure uses magnetic separation technology, the protocol does not require vacuum filtration. This makes kit extremely amenable to automation. Plasmid DNA purified with this system is most commonly used in Sanger Sequencing and PCR amplification.
Details
Specifications
Features
Specifications
Main Functions
Isolation up to 20µg plasmid DNA from 1-3ml bacterial culture
Applications
Enzyme digestion, sequencing, PCR and labeling, etc.
Purification technology
Magnetic beads technology
Process method
Manual or automatic
Sample type
Conventional plasmid, plasmid≤30KB
Sample amount
1-3ml
Elution volume
≥50μl
Principle
This product is based on the purification method of high binding magnetic particles. The sample is lysed and digested under the action of lysate and Lysozyme. DNA is released into the lysate. After adding magnetic particles and binding solution, DNA will be adsorbed on the surface of magnetic particles, and impurities such as proteins will be removed without adsorption.The adsorbed particles were washed with washing solution to remove proteins and impurities, washed with ethanol to remove salts, and finally DNA was eluted by Elution Buffer.
Advantages
1. Suitable for extracting plasmids from 1-5ml or <3ml YT medium. 2. The same amount of buffer 1, 2, and 3 avoids errors caused by adjusting the pipette, making it convenient to use in conjunction with automated workstations. 3. Containing buffer 1 for washing, reducing the problem of false high production. 4. The purified plasmid can be directly used for sequencing, enzyme digestion, PCR, and other applications.
Kit Contents
Contents
P181102
P181103
P181104
Purification Times
100 Preps
500 Preps
5000 Preps
RNase A
10 mg
50 mg
2 x 250 mg
Buffer P1
30 ml
150 ml
2 x 750 ml
Buffer P2
30 ml
150 ml
2 x 750 ml
Buffer N3
30 ml
150 ml
2 x 750 ml
Buffer PW1
35 ml
180 ml
2 x 900 ml
MagPure Particle NB*
2.2 ml
11 ml
2 x 60 ml
Storage and Stability
RNase A and MagPure Particle NB should be stored at 2-8°C upon arrival. However, short-term storage (up to 24 weeks) at room temperature (15-25°C) does not affect its performance. The remaining kit components can be stored dry at room temperature (15-25°C) and are stable for at least 18 months under these conditions. After addition of RNase A, Buffer P1 is stable for 6 months when stored at 2-8°C.
Experiment Data
Document
The MagPure Plasmid purification system uses the paramagnetic bead technology for high-throughput preparation of high-copy or low-copy plasmid DNA from E. coli cells. This kit also can be used with fosmid and BAC vector-based constructs. The system uses alkaline lysis followed by a MagPure purification to differentially bind plasmid DNA to paramagnetic beads. While the DNA is bound to the beads, contaminants can be rinsed away using a simple washing procedure. Because MagPure uses magnetic separation technology, the protocol does not require vacuum filtration. This makes kit extremely amenable to automation. Plasmid DNA purified with this system is most commonly used in Sanger Sequencing and PCR amplification.
