Molecular Biology

electrophoresis gel matrix


 

 

 

Acrylamides solutions

  • Ready to use 40% solution.

  • Prepared with the highest quality products : 4X acrylamide, 2X bis-acrylamide.

  • No hazard powder.

Liquid Acrylamide products were designed to replace powdered materials with convenient, "user friendly" solutions. These solutions are provided in a ready-to-use format, thereby eliminating inhalation hazards associated with handling acrylamide and bis-acrylamide powders.

Liquid Acrylamides produce highly reproducible gels with excellent band mobility and resolution. Concentrations are carefully controlled for maximum lot-to-lot consistency and all solutions are 0.2 um micro-filtered prior to packaging.

Liquid Acrylamide products are prepared from Ultra Pure Grade components in specially treated, deionized water and are guaranteed stable for at least one year when properly stored.

Acrylamide/Bis-Acrylamide 19:1

is a 40% solution containing 38% (w/v) acrylamide and 2% (w/v) bis-acrylamide. Optimized for nucleic acid electrophoresis. Final ratio of monomer to cross-linker is 19:1.

Acrylamide/Bis-Acrylamide 29:1

is a 40% solution containing 38.67% (w/v) acrylamide and 1.33% (w/v) bis-acrylamide. Excellent for many protein electrophoresis applications and can also be used for nucleic acid electrophoresis. Final monomer to cross-linker ratio is 29:1.

Acrylamide/Bis-Acrylamide 37.5:1 (30:0.8)

is a solution of 38.96% (w/v) acrylamide and 1.04% (w/v) bis-acrylamide. Optimized for most protein separations. Final ratio is 37.5:1 (30:0.8).

Security Sheet

Acrylamides

UP873376

500ml

Solution 4X-40%

UP873377

2x500ml

Bis-Acrylamide

UP864965

500ml

Solution 2%

UP864966

2x500ml

Acrylamides/Bis-Acrylamide 19:1

UP86489B

500ml

Solution 40%

UP86489C

2x500ml

Acrylamides/Bis-Acrylamide 29:1

UP864927

500ml

Solution 40%

UP864928

2x500ml

Acrylamides/Bis-Acrylamide 37.5:1

UP864937

500ml

Solution 40%

UP864938

2x500ml

 

Other biochemicals for electrophoresis

Ammonium Persuflate

UP306098

4x25g

ACS Grade

-

(NH4)2S2O8

CAS [7727-57-0]

MW 228.20

Purity 98.0 %

Titrable Free Acid < 0.04 meq/g

Storage at store at room temperature

Formamide, deionized

UP07099

TEMED

UP15413D

25ml

(N,N,N’,N’-TETRAMETHYLETHYLENEDIAMINE)

Ultra pure grade

C6H16N2

CAS [10-18-9]

MW 116.21

Purity (Anhydrous Basis) : 99.0 %

Storage at store at room temperature.

-

SDS, powder

UP64910

SDS, 20% solution

UP89682

Urea

 

Agaroses

Agarose MB

UPS54180

100g

UPS54181

250g

for analytical electrophoresis in Molecular Biology

Applications

Agarose UPTIMA has been specially designed for analytical electrophoresis in routine Molecular Biology analysis. Separation range is 0.2 - 22 Kbp, depending on agarose concentration and buffer used for electrophoresis.

 

Fig1.

Four samples were amplified using Cytochrome b specific primers (lanes 1-4), using Uptima UptiTherm DNA Polymerase (Cat.No. UPS5 3661).

The 358 bp product was separated by electrophoresis using Uptima agarose (1.5% gel) in TBE buffer for 35 min (5V/cm). The Uptima agarose shows an exceptional resolution as well as clarity and performance, even for the visualisation of 100 bp molecular weight marker (Cat.No. UPS54811).

Technical Information

Appearance

White fine powder

Gel strength (1%)

1200 gr / cm2

Gelling range (1%)

36-39ºC

Melting range

87 - 89 ºC

EEO (relative mobility) (1%)

< 0.10

Sulphates

< 0 - 10 %

DNase, Rnase

Non detected

Protease activities

Non detected

Quality control

Each lot is thoroughly controled to ensure maximum performance and lot to lot reproducibility.

Store at room temperature.

Agarose HR

UPS54200

50g

UPS54201

100g

for high resolutionl electrophoresis

Applications

Agarose UPTIMA has been specially designed for analytical electrophoresis in routine Molecular Biology analysis. Separation range is 20 - 2000bp, depending on agarose concentration and buffer used for electrophoresis.

 

Fig 2.

Four samples were amplified using cytochrome b specific primers (lanes 1-4), using Uptima DNA Polymerase (Cat.No. UPS53661). The 358bp product was separated by electrophoresis using Uptima HR agarose 1.5% in TBE buffer for 35 min(5V/cm2).

The Uptima agarose HR shows an exceptional resolution as well as clarity and performance, even for the visualisation of 100 bp molecular weight marker (UPS54811).

Technical Information

Appearance

White fine powder

Gel strength (1%)

2000 gr / cm2

Gelling range (1%)

36-38ºC

Melting range

87 - 89 ºC

EEO (relative mobility) (1%)

< 0.15

Sulphates

< 0 - 15 %

DNase, Rnase

Non detected

Protease activities

Non detected

Quality control

Each lot is thoroughly controled to ensure maximum performance and lot to lot reproducibility.

Store at room temperature.

Agarose HR0.7

UPS54252

1L

UPS54253

2L

for high resolution electrophoresis using 0.7% standard agarose

Applications

Uptima Agarose HR0.7 (0.7% standard agarose) substitutes high-resolution agaroses for the discrimination of DNA fragments <500bp.

Revolutionary: up to 6 - 10 bp discrimination.

Savvy: cuts down agarose costs.

DNA can be purified from the Agarose HR0.7 Matrix using standard methods.

Fast and easy to use.

Agarose HR0.7 Matrix kit includes Uptima MB Agarose.

Quality control

Each lot is thoroughly controled to ensure maximum performance and lot to lot reproducibility.

Store at <25°C

Fig 3.

Agarose HR0.7 gel showing duplicate samples of three molecular ladders : FX174-Hinfl (lanes 1-2, Cat. UPS54781), pBR322/BsuRI (3-4, Cat. UPS54791), and 100 bp-ladder (5-6, Cat.UPS54811). Picture to the left depicts low-molecular weight bands with sharper contrast.

 

Related product

Ethidium Bromide

UP89244B

10ml

10mg/ml solution

C21H20BrN3

CAS [1239-45-8]

MW 394,32

Ethidium Bromide solution is the safer than powder and most convenient means to prepare gels, solutions and gradients for your molecular biology applications. Ethidium bromide intercalates double-stranded DNA and RNA2. The fluorescence of EtBr increases 21-fold upon binding to double-stranded RNA and 25-fold on binding double-stranded DNA so that destaining the background is not necessary with a low stain concentration (10 mg/ml). Ethidium bromide has been used in a number of fluorimetric assays for nucleic acids3-5. It has been shown to bind to single-stranded DNA (although not as strongly) and triple-stranded DNA6.

 

Ethidium Bromide is a nucleic acid intercalating agen and frameshift mutagen1. It can also be used in conjunction with acridine orange to differentiate between viable, apoptotic and necrotic cells3.

Literature :

1- Scaria, P.V. , Shafer, R.H., Binding of ethidium bromide to a DNA triple helix. Evidence for intercalation J. Biol. Chem. 266, 5417 (1991)

2- Sambrook, J., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor, (1989), 6-44, 6

3- Karsten, U. , Wollenberger, A., Improvements in the ethidium bromide method for direct fluorometric estimation of DNA and RNA in cell and tissue homogenates Anal. Biochem. 77, 464 (1977)

4- El-Hamalawi, A., The fluorometric determination of nucleic acids in pea seeds by use of ethidium bromide complexes. Anal. Biochem. 67, 384 (1975)

5- Moore, S.P. , Sutherland, B.M., A densitometric nondestructive microassay for DNA quantitation Anal. Biochem. 144, 15 (1985)

6- Severini, A. , Morgan, A.R., An assay for proteinases and their inhibitors based on DNA/ethidium bromide fluorescence Anal. Biochem. 193, 83 (1991)

 

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