Naar de inhoud springen Naar het navigatiemenu springen

ROTI®Load DNAstain 2 SYBR® Green, 1.8 ml, 1 x 1.8 ml

6x conc., ready-to-use
Icon_ready-to-use Ready-to-use products and reagents
VE
Verp.
Verpakking
Density (D) ~1,12 g/cm³
Storage temp. -20 °C
Transport temp. ambient temp.
WGK 1

DNA-gel loading buffer with fluorescent DNA-dye SYBR® Green. For fragments of 100-2000 bp.
Contains: Tris, EDTA, xylencyanol, tartrazine, SYBR® Green.
1.8 ml are sufficient for gel run and staining of approx. 1,800 lanes (5 µl sample + 1 µl loading buffer).

53,65 €/VE 

Excl. btw | 1,8 ml Per VE

Bestelnr. 1CN6.1

Op voorraad
Vrij van verzendingskosten vanaf 250 €
Snelle en betrouwbare levering!
Vanaf 6 VE 50,97 €/VE
Vanaf 24 VE 48,28 €/VE

Productdetails



ROTI®Load DNAstain 2 SYBR® Green 6x conc., ready-to-use

Technische informatie
Activeringsmax. (DNA-gebonden) ~320 nm
470-500 nm
Aantal sporen ca. 1000/ml 
Emissiemax. (DNA-gebonden) 525 nm 
Kleurstof Xylene cyanole, tartrazine, SYBR® Green 
Incl. DNA-kleuring ja 
Sensitiviteit 0,01 ng/band
Toepassing Simultaneous gel staining, medium fragments 
ROTI®Load DNAstain 2 SYBR® Green
Geselecteerde hoeveelheid:   0
  1. Tussentotaal:  0.00
Bestelnr. VE Verp. Verpakking Prijs Hoeveelheid
1CN6.1 1,8 ml plastic 1 x 1.8 ml

53,65 €

1CN6.2 9 ml plastic 5 x 1.8 ml

166,65 €

Op voorraad
Beschikbaar
In bestelling
Niet meer verkrijgbaar
Leveringsdatum onbekend
Geselecteerde hoeveelheid:   0
  1. Tussentotaal:  0.00

Downloads / MSDS


Algemene informatie

Selecting a Suitable ROTI®Load Gel Loading Buffer for Nucleic Acids

Care should be taken to ensure that the dyes contained in the gel stop before smallest relevant DNA bands. This ensures that the buffer can be stopped in time. However, the selected dyes may overlay the bands shown. In this case, select a loading buffer that does not contain any unwanted dyes.
Bromophenol blue and xylene cyanol can be used as colour markers in all standard gels. If a relevant band is overlaid by one of these colour markers, choose a gel loading buffer containing Orange G. If small fragments are to be assayed, the gel loading buffer should contain Orange G in order to mark the run. If relevant bands are overlaid, however, a choice can be made between bromophenol blue or xylene cyanol depending on the size of the bands. A loading buffer without xylene cyanol is usually used for assaying large fragments.

Glycerine is the standard reagent for increasing the density of samples.
Ficoll® 400 produces particularly well-defined bands.


Summary Staining of Nucleic Acid in Gels

Product Sensitivity Description Excitation
Ethidium bromide solution 0.5-5 ng/band Standard fluorescent staining 254-330 nm, 500 nm UV- and blue light
SYBR® Green DNA dye 0.01 ng/band Non-toxic, green fluorescent staining 254 nm and 495 nm UV- and blue light
ROTI®GelStain 0.3 ng/band Non-toxic, green fluorescent staining 302 nm and 490 nm UV- and blue light
ROTI®GelStain Red 0.3 ng/band Non-toxic, red fluorescent staining 310 nm, 540 nm UV- and blue light
ROTI®Methylene blue staining concentrate 10 ng/band Reversible, non-toxic blue staining White light
ROTI®Black N <0.1 ng/band Silver staining of DNA polyacrylic amide gels White light

Analysecertificaten

Hier kunt u uw analysecertificaat voor het geselecteerde product zoeken en downloaden. Geef een chargenummer op.
De volgende analysecertificaten werden gevonden:

Notes on the product

Appearancegreen solution
Each batch is functionally tested for its suitability in electrophoresis.