Random Primers
Random Primers
Invitrogen™

Random Primers

Random Primers are oligodeoxyribonucleotides (mostly hexamers) used to prepare labeled DNA probes from templates for filter hybridization or in situRead more
Have Questions?
Catalog NumberQuantity
48190011100 μL
Catalog number 48190011
Price (EUR)
222,00
Each
-
Add to cart
Quantity:
100 μL
Recurring order eligible. Learn more »
Price (EUR)
222,00
Each
Add to cart
Ask our AI about this Product

Random Primers are oligodeoxyribonucleotides (mostly hexamers) used to prepare labeled DNA probes from templates for filter hybridization or in situ hybridization and to prime mRNAs with or without poly(A) for cDNA synthesis. These primers are truly random and are suitable for DNA synthesis using Klenow fragments with DNA templates or for cDNA synthesis using reverse transcriptase with mRNA templates. To avoid storage buffer interference, Random Primers are supplied in a low-salt-concentration buffer.

Performance and quality testing: Incorporation of a radioactively labeled nucleotide is verified using control DNA in a Random Primers labeling reaction

For Research Use Only. Not for use in diagnostic procedures.
Specifications
For Use With (Application)cDNA Synthesis
FormLiquid
Product TypePrimer
Quantity100 μL
Shipping ConditionApproved for shipment on Wet or Dry Ice
Concentration3 μg/μL
PrimerRandom
Unit SizeEach
Contents & Storage
• Random Primers in 3 mM Tris-HCl, 0.2 mM EDTA (100 μL at 3 μg/μL)

Store at –20°C.
Guaranteed stable for 6 months when properly stored.
Have questions about this product? Ask our AI assisted search.
Can I use CTAB rather than SDS in my sample buffer?
Where do I find buffer recipes for your precast protein gels?
Why is LDS (lithium dodecyl sulfate) used in the 4X NuPAGE sample buffer instead of SDS?
What is the recipe for traditional Laemmli Buffer?
If a Tricine gel is accidentally run with buffers used in the Tris-Glycine system, what will happen and why?
This is an AI-powered search and may not always get things right. You can help us make it better with a thumbs up or down on individual answers or by selecting the “Give feedback" button. Your search history and customer login information may be retained by Thermo Fisher and processed in accordance with our Privacy Notice.

瀏覽此商品的人,也瀏覽



Documents & Downloads

Certificates

Lot #Certificate TypeDateCatalog Number(s)
3046923Certificate of AnalysisMar 20, 202548190011
2321900Certificate of AnalysisJan 31, 202548190011
2984116Certificate of AnalysisJan 31, 202548190011
2505846Certificate of AnalysisJan 30, 202548190011
2367817Certificate of AnalysisJan 30, 202548190011
5 results displayed, search above for a specific certificate

Safety Data Sheets

Product Information

Frequently asked questions (FAQs)

Yes, we do offer Random Primers as a stand-alone item: Cat. No. 48190011.

The following components are available as stand-alone items:

- Superscript III Reverse Transcriptase (Cat. Nos. 18080093, 18080044, 18080085)
- Oligo (dT)20 Primer (Cat. No. 18418020)
- Random hexamers (Cat. No. 48190011)
- 10 mM dNTP Mix (Cat. Nos. 18427013, 18427088)
- RNAseOUT Recombinant Ribonuclease Inhibitor (Cat. No. 10777019)
- E. coli RNAse H (Cat. Nos. 18021014, 18021071)

The concentration of Random Primers (Cat. No. 48190011) is 1500 pmol/µL or 1.5 mM.

Find additional tips, troubleshooting help, and resources within our Reverse Transcription and RACE Support Center.

Citations & References (6)

Citations & References
Abstract
Global Expression Profiling of Acetate-grown Escherichia coli.
Authors: Oh Min-Kyu; Rohlin Lars; Kao Katy C; Liao James C;
Journal:J Biol Chem
PubMed ID:11815613
'This study characterized the transcript profile of Escherichia coli in acetate cultures using DNA microarray on glass slides. Glucose-grown cultures were used as a reference. At the 95% confidence level, 354 genes were up-regulated in acetate, while 370 genes were down-regulated compared with the glucose-grown culture. Generally, more metabolic genes ... More
RasGRP, a Ras guanyl nucleotide- releasing protein with calcium- and diacylglycerol-binding motifs.
Authors:Ebinu JO, Bottorff DA, Chan EY, Stang SL, Dunn RJ, Stone JC
Journal:Science
PubMed ID:9582122
RasGRP, a guanyl nucleotide-releasing protein for the small guanosine triphosphatase Ras, was characterized. Besides the catalytic domain, RasGRP has an atypical pair of EF hands that bind calcium and a diacylglycerol (DAG)-binding domain. RasGRP activated Ras and caused transformation in fibroblasts. A DAG analog caused sustained activation of Ras-Erk signaling ... More
Class II histone deacetylases act as signal-responsive repressors of cardiac hypertrophy.
Authors:Zhang CL, McKinsey TA, Chang S, Antos CL, Hill JA, Olson EN,
Journal:Cell
PubMed ID:12202037
The heart responds to stress signals by hypertrophic growth, which is accompanied by activation of the MEF2 transcription factor and reprogramming of cardiac gene expression. We show here that class II histone deacetylases (HDACs), which repress MEF2 activity, are substrates for a stress-responsive kinase specific for conserved serines that regulate ... More
Improvements in siRNA properties mediated by 2'-deoxy-2'-fluoro-beta-D-arabinonucleic acid (FANA).
Authors:Dowler T, Bergeron D, Tedeschi AL, Paquet L, Ferrari N, Damha MJ,
Journal:Nucleic Acids Res
PubMed ID:16554553
RNA interference (RNAi) has emerged recently as an efficient mechanism for specific gene silencing. Short double-stranded small interfering RNAs (siRNAs) are now widely used for cellular or drug target validation; however, their use for silencing clinically relevant genes in a therapeutic setting remains problematic because of their unfavourable metabolic stability ... More
Use of an in vivo reporter assay to test for transcriptional and translational fidelity in yeast.
Authors: Shaw Randal J; Bonawitz Nicholas D; Reines Daniel;
Journal:J Biol Chem
PubMed ID:12006589
Eukaryotic RNA polymerase II and Escherichia coli RNA polymerase possess an intrinsic ribonuclease activity that is stimulated by the polymerase-binding proteins SII and GreB, respectively. This factor-activated hydrolysis of nascent RNA has been postulated to be involved in transcription elongation as well as removal of incorrect bases misincorporated into RNA. ... More
6 total citations

Share catalog number, name or link

1x1 image pixel for data collection