2012 Promega catalogue
2012 Promega catalogue
2012 Promega catalogue
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Life<br />
Science<br />
Catalog<br />
<strong>2012</strong><br />
Worldwide Contact List<br />
Section<br />
Contents<br />
Table of<br />
Contents<br />
Cell Signaling<br />
94<br />
DNA 5´ End-Labeling System<br />
Product Size Cat.# Price ($)<br />
DNA 5´ End-Labeling System 10 reactions U2010 144.00<br />
For Laboratory Use.<br />
Description: The DNA 5´ End-Labeling System is a complete system for<br />
phosphorylating both double- and single-stranded DNA and RNA with T4<br />
Polynucleotide Kinase and [γ- 32 P]ATP. The system includes enzymes, buffers<br />
and control DNA standards to measure reaction efficiencies. Calf Intestinal<br />
Alkaline Phosphatase is included for removal of the 5´-phosphate prior to<br />
labeling with T4 Polynucleotide Kinase.<br />
Features:<br />
• Convenient: Can use to label both single-stranded and double-stranded<br />
DNA and RNA.<br />
• Complete: System includes enzymes, buffers and control DNA standards<br />
for measuring reaction efficiencies (except radionucleotides).<br />
• Flexible: Works with [γ- 32 P]ATP, [γ- 33 P]ATP or [γ- 35 S]ATP.<br />
Storage Conditions: Store at –20°C.<br />
Protocol Part#<br />
DNA 5´ End-Labeling System Technical Bulletin TB096<br />
Prime-a-Gene ® Labeling System<br />
Product Size Cat.# Price ($)<br />
Prime-a-Gene ® Labeling System<br />
Available Separately<br />
30 reactions U1100 282.00<br />
Nuclease-Free Water 150 ml P1195 125.00<br />
Labeling 5X Buffer 300 µl U1151 58.00<br />
U1100, U1151 For Laboratory Use. P1195 For Research Use Only. Not for Use in Diagnostic<br />
Procedures.<br />
Description: The Prime-a-Gene ® Labeling System provides a complete set<br />
of complementary reagents, including Labeling 5X Buffer that contains random<br />
synthetic hexadeoxynucleotide primers for random-primed labeling of linear<br />
template DNA with radionucleotides. As little as 25ng of input DNA can be used<br />
to generate probes with specific activities >1 × 10 9 cpm/μg.<br />
Storage Conditions: Store at –20°C.<br />
Protocol Part#<br />
Prime-a-Gene ® Labeling System Technical Bulletin<br />
TB049<br />
Ribonuclease H<br />
Product Size Conc. Cat.# Price ($)<br />
Ribonuclease H 50 u 0.5–2 u/µl M4281 207.00<br />
For Laboratory Use.<br />
250 u 0.5–2 u/µl M4285 884.00<br />
Description: Ribonuclease H (RNase H) is an endonuclease that specifically<br />
hydrolyzes the phosphodiester bonds of RNA hybridized to DNA to produce<br />
3´-OH and 5´-P-terminated products. It will not degrade single-stranded nucleic<br />
acids, double-stranded DNA or double-stranded RNA.<br />
Storage Conditions: Store at –20°C.<br />
RNase ONE Ribonuclease<br />
Product Size Conc. Cat.# Price ($)<br />
RNase ONE Ribonuclease 1,000 u 5–10 u/µl M4261 177.00<br />
For Laboratory Use.<br />
5,000 u 5–10 u/µl M4265 665.00<br />
Description: RNase ONE Ribonuclease is a 27kDa periplasmic enzyme<br />
from E. coli that catalyzes the degradation of RNA to cyclic nucleotide mono-<br />
phosphate (NMP) intermediates. Slower hydrolysis further catalyzes the<br />
degradation of these intermediates to 3´-NMPs. RNase ONE Ribonuclease is<br />
one of the few known RNases that can cleave a phosphodiester bond between<br />
any two ribonucleotides. RNase ONE Ribonuclease may be used to remove<br />
RNA from DNA preparations, for RNase protection assays and for mapping or<br />
quantitation of RNA by selective cleavage of single-stranded regions.<br />
Features:<br />
• Flexible: RNase ONE Ribonuclease has the ability to cleave phosphodiester<br />
bonds between any two ribonucleotides.<br />
• Provided with 10X Reaction Buffer: 100mM Tris-HCl (pH 7.5 at 25°C),<br />
50mM EDTA, 2M sodium acetate.<br />
Storage Conditions: Store at –20°C. Do not freeze at –70°C. Do not store<br />
on dry ice.<br />
RQ1 RNase-Free DNase<br />
Product Size Conc. Cat.# Price ($)<br />
RQ1 RNase-Free DNase<br />
For Laboratory Use.<br />
1,000 u 1 u/µl M6101 86.00<br />
Description: RQ1 RNase-Free DNase is a preparation of deoxyribonuclease I<br />
that degrades single-stranded or double-stranded DNA to produce 3´-hydroxyl<br />
oligonucleotides. This preparation is qualified for use in applications where<br />
maintaining the integrity of RNA is critical.<br />
Features:<br />
• Convenient: 10X Reaction Buffer (400mM Tris-HCl [pH 8.0 at 25°C],<br />
100mM MgSO 4, 10mM CaCl 2) and Stop Buffer (20mM EGTA [pH 8.0 at<br />
25°C]) are provided.<br />
Storage Conditions: Store at –20°C.<br />
Protocol Part#<br />
RQ1 RNase-Free DNase Protocol 9PIM610<br />
For complete and up-to-date product information visit: www.promega.com/catalog