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Cytiva Amersham™ Megaprime™ DNA Labeling System
For labeling DNA probes to specific activities >1 x 109dpm/μg in 10 minutes
650.00 € - 1119.00 €
Specifications
| Content And Storage | -15°C to -30°C |
|---|---|
| For Use With (Application) | Membrane hybridization |
| Product Code | Brand | Product Type | No. of Reactions | Includes | Price | Quantity & Availability | |||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Product Type | No. of Reactions | Includes | Price | Quantity & Availability | |||
|
10575155
|
Cytiva
RPN1605 |
Megaprime DNA Labeling System, dNTP (for use with any radioactively labeled nucleotide) | 60 | Primer solution 300μL, Labeling Buffer dATP, dGTP and dTTP in Tris HCl pH7.5, 2-mercaptoethanol and MgCl2, Nucleotide solutions dATP, cCTP, dGTP, dTTP in Tris HCl pH 8, 0.5mM EDTA 240μL, Reaction Buffer A 10 x concentra | N/A | ||||
|
10175804
|
Cytiva
RPN1607 |
Megaprime DNA Labeling System, dCTP (for use with labeled dCTP) | 60 | Primer solution 300μL, Labeling Buffered ATP, dGTP and dTTP in Tris HCl pH7.5, 2-mercaptoethanol and MgCl2 600μL, Nucleotide solutions dATP, cCTP, dGTP, dTTP in Tris HCl pH 8, 0.5mM EDTA, Reaction Buffer A 10 x concentr | N/A | ||||
|
10025174
|
Cytiva
RPN1604 |
Megaprime DNA Labeling System, dNTP (for use with any radioactively labeled nucleotide) | 30 | Primer solution 150μL; Labeling Buffer dATP, dGTP and dTTP in Tris HCl pH7.5, 2-mercaptoethanol and MgCl2 Nucleotide solutions: dATP, cCTP, dGTP, dTTP in Tris HCl pH 8, 0.5mM EDTA 120μL, Reaction Buffer A 10 x concentra | N/A | ||||
|
10714367
|
Cytiva
RPN1606 |
Megaprime DNA Labeling System, dCTP (for use with labeled dCTP) | 30 | Primer solution 150μL, Labeling Buffer dATP, dGTP and dTTP in Tris HCl pH7.5, 2-mercaptoethanol and MgCl2 300μL, Nucleotide solutions dATP, cCTP, dGTP, dTTP in Tris HCl pH 8, 0.5mM EDTA, Reaction Buffer A 10 x concentra | N/A | ||||
Description
Megaprime™ DNA Labeling Systems are used for rapid, random-prime labeling from as little as 25ng substrate DNA.
- Features cloned Klenow fragment and random nonamers in the random-prime labeling technique
- No need to remove unincorporated nucleotides before hybridization
- Protocols for labeling directly from low melting point agarose
Specifications
| -15°C to -30°C | |
| Membrane hybridization |