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引用和文献 (15)
Invitrogen™
Novex™ TBE Gels, 4–20%
Novex™ TBE Gels 4–20% 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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| 货号 | 孔 |
|---|---|
| EC62255BOX | 15孔 |
| EC6225BOX | 10孔 |
| EC62252BOX | 12孔 |
货号 EC62255BOX
价格（CNY)
2,137.00
Each
孔:
15孔
价格（CNY)
2,137.00
Each
Novex™ TBE Gels 4–20% 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 25–300 bp.
- DNA 片段可以被清晰地分离出明显紧密的条带
- 适合在 XCell SureLock™ Mini-Cell 小型电泳仪上运行
- 使用高纯度 Tris 碱、硼酸、EDTA、丙烯酰胺、双丙烯酰胺、TEMED 和 APS 制作而成
琼脂糖凝胶电泳、DNA 和 RNA 纯化及分析、核酸凝胶电泳和印迹杂交
For Research Use Only. Not for use in diagnostic procedures.
规格
描述Novex TBE Gels, 4 to 20%, 15-well
产品类型TBE 凝胶
数量10 块凝胶/盒
样品类型Double-stranded DNA (dsDNA)
运输条件湿冰
适用于（设备）XCell SureLock Mini-Cell
凝胶百分比4 至 20%
凝胶类型TBE 胶
分离范围25 to 300 bp
孔15孔
Unit SizeEach
内容与储存
• 货号是指一盒10块凝胶
在 4°C 下储存。
在 4°C 下储存。
常见问题解答 (FAQ)
我能否对TBE凝胶染色？如何染色？
TBE凝胶上可见的最小片段长度是多少？
TBE凝胶中的EDTA浓度是多少？甘油呢？
我可以对TBE凝胶或TBE-尿素凝胶染色吗？如何染色？
TBE凝胶的电泳条件（电压，电流，电泳时间等）是什么？
引用和文献 (15)
引用和文献
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