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Citations & References (15)
Invitrogen™
Novex™ TBE Gels, 6%
Novex™ TBE Gels 6% are designed to run on the XCell SureLock™ Mini-Cell and provide high-resolution analysis of restriction digests and PCR products.
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| Catalog Number | Wells |
|---|---|
| EC62655BOX | 15-well |
| EC6261BOX | 1-well |
| EC6265BOX | 10-well |
| EC62652BOX | 12-well |
Catalog number EC62655BOX
Price (EUR)
276,65
Online Exclusive
285,00Save 8,35 (3%)
Each
Wells:
15-well
Price (EUR)
276,65
Online Exclusive
285,00Save 8,35 (3%)
Each
Novex™ TBE Gels 6% provide high-resolution analysis of restriction digests and PCR products. Designed to run on the XCell SureLock™ Mini-Cell, the polyacrylamide gels give sharp, clearly resolved, intense bands, and provide separations of double-strand DNA fragments from 65–250 bp.
Novex TBE Gels are available in a variety of well formats and gel percentages and can be stained by silver staining, ethidium bromide, and SYBR™ Green staining techniques after electrophoresis.
Advantages of TBE Gels for nucleic acid separation:
• High resolution and sensitivity with lower background staining
• Requires ∼10% sample concentration and volume of large or agarose gels
• Efficient blotting
• Easy extraction of DNA from gels
• Gel extraction does not interfere with enzymatic reactions
• Accurate and reproducible results
Formulation
Novex TBE gels are manufactured with high-purity Tris base, boric acid, EDTA, acrylamide, bisacrylamide, TEMED, and APS.
Recommended buffers
For optimum performance, Novex™ TBE Running Buffer and Novex™ Hi-Density TBE Sample Buffer are strongly recommended for use with these gels. Novex Hi-Density TBE Sample Buffer contains the tracking dyes Bromophenol Blue and Xylene Cyanol as well as the density agent Ficoll™, which yields sharper and straighter bands than conventional density agents.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
DescriptionNovex TBE Gels, 6%, 15-well
For Use With (Equipment)XCell SureLock Mini-Cell
Quantity10 Gels/Box
Sample TypeDouble-stranded DNA (dsDNA)
Shipping ConditionWet Ice
Gel Percentage6%
Gel TypeTBE
Product TypeTBE Gel
Separation Range65 to 250 bp
Wells15-well
Unit SizeEach
Contents & Storage
• Catalog number refers to a single box of 10 gels
Store at 4°C.
Store at 4°C.
Citations & References (15)
Citations & References
Abstract
Prevalence and correlates of GB virus C infection in HIV-infected and HIV-uninfected pregnant women in Bangkok, Thailand.
Journal:J Med Virol
PubMed ID:21108337
'GB virus C (GBV-C) is an apathogenic virus that has been shown to inhibit HIV replication. This study examined the prevalence and correlates of GBV-C infection and clearance in three cohorts of pregnant women in Thailand. The study population consisted of 1,719 (1,387 HIV-infected and 332 HIV-uninfected) women from three
An in vitro DNA double-strand break repair assay based on end-joining of defined duplex oligonucleotides.
Journal:Methods Mol Biol
PubMed ID:22941624
'DNA double-strand breaks (DSBs) are caused by endogenous cellular processes such as oxidative metabolism, or by exogenous events like exposure to ionizing radiation or other genotoxic agents. Repair of these DSBs is essential for the maintenance of cellular genomic integrity. In human cells, and cells of other higher eukaryotes, DSBs
Smooth muscle phenotypic diversity is mediated through alterations in myocardin gene splicing.
Journal:J Cell Physiol
PubMed ID:21792927
'Myocardin (MYOCD) is a smooth and cardiac muscle-specific transcriptional coactivator that is required for the proper expression of contraction-related genes. Through its function to transactivate effector genes, MYOCD plays an essential role in mediating the switch between contractile and non-contractile phenotypes, particularly in smooth muscle cells (SMC). There are at
Genome wide full-length transcript analysis using 5' and 3' paired-end-tag next generation sequencing (RNA-PET).
Journal:Methods Mol Biol
PubMed ID:22113299
'RNA-PET is a paired end tag (PET) sequencing method for full-length mRNA transcripts analysis using the next generation sequencer platforms such as Illumina GA and SOLiD. Unlike RNA-Seq method that sequences randomly sheared shotgun RNA short fragments, RNA-PET captures and sequences the 5'' and 3'' end tags of full-length cDNA
Rapid, low-input, low-bias construction of shotgun fragment libraries by high-density in vitro transposition.
Journal:Genome Biol
PubMed ID:21143862
We characterize and extend a highly efficient method for constructing shotgun fragment libraries in which transposase catalyzes in vitro DNA fragmentation and adaptor incorporation simultaneously. We apply this method to sequencing a human genome and find that coverage biases are comparable to those of conventional protocols. We also extend its