UltraPure™ 琼脂糖-1000
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UltraPure™ 琼脂糖-1000
Invitrogen™

UltraPure™ 琼脂糖-1000

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UltraPure™ 琼脂糖-1000 是一种多糖(参见结构),用于在琼脂糖凝胶电泳中基于大小分离核酸。UltraPure™ 琼脂糖 1000 专门配制用于小分子 (•非常适合分析和回收小分子了解更多信息
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货号数量
16550100100 g
货号 16550100
价格(CNY)
2,206.00
飞享价
Ends: 31-Dec-2025
6,438.00
共减 4,232.00 (66%)
Each
添加至购物车
数量:
100 g
请求批量或定制报价
价格(CNY)
2,206.00
飞享价
Ends: 31-Dec-2025
6,438.00
共减 4,232.00 (66%)
Each
添加至购物车
UltraPure™ 琼脂糖-1000 是一种多糖(参见结构),用于在琼脂糖凝胶电泳中基于大小分离核酸。UltraPure™ 琼脂糖 1000 专门配制用于小分子 (<1,000 bp) DNA、RNA 和 PCR 片段的高分辨率分离。该标准熔点琼脂糖可分离大小低至 10bp 的不同 DNA 片段。使用 UltraPure™ 琼脂糖 1000 的优势:

•非常适合分析和回收小分子 DNA 和 RNA 片段
• 强凝胶结构可更好地进行处理
• 更高的透明度可增强片段的能见度

改善包装
新型环保包装使用的塑料量比原装瓶少 75%(参见图)。这意味着在制造过程中消耗更少的能源和原材料,垃圾填埋场的废弃物也更少。此外,简易倒口减少了溢出和污染的可能性。

性能和质量检测
UltraPure™ 琼脂糖 1000 的性能经评价可满足外观、水分、凝胶强度、胶凝温度、熔化温度、硫酸盐含量、电内渗和 DNase/RNase 分析的质量标准。

注:UltraPure™ 琼脂糖 10000(货号 16550-100)是先前销售的货号 10975-035 产品的替换产品。
仅供科研使用。不可用于诊断程序。
规格
适用于(应用)核酸凝胶电泳、印迹
形式粉末
凝胶兼容性琼脂糖凝胶
环保功能绿色可持续包装
熔点标准熔点
产品线UltraPure
产品类型琼脂糖
数量100 g
运输条件室温
分离范围50 bp - 1 kb
Unit SizeEach
内容与储存
1 袋,含 100 g UltraPure™ 低熔点琼脂糖。在室温下储存。

常见问题解答 (FAQ)

我想自己灌胶,你们推荐用什么琼脂糖?

我们的UltraPure琼脂糖是标准熔点琼脂糖,适用于DNA和RNA片段的常规分离和分析,分离范围为500–23,000bp。UltraPure琼脂糖1000是特制的琼脂糖,为PCR片段和其它短DNA片段提供较高的分辨率。我们也提供UltraPure低熔点琼脂糖,是在65°C或更低的温度下分离10到1000 bp DNA片段的理想选择。

I want to pour my own gels. Which agarose should I use?

Our UltraPure Agarose is standard melting-point agarose designed for routine separation and analysis of DNA and RNA fragments in the 500-23,000 nt range. UltraPure Agarose 1000 is a specialized agarose that provides higher resolution of PCR fragments and other short DNA fragments. We also offer an UltraPure Low Melting Point Agarose, which is ideal for resolving DNA fragments from 10 to 1,000 bp with a low melting temperature of 65°C or less.

How can generation of replication competent adenoviruses be avoided when using your pSilencer adeno 1.0-CMV System?

Although there is only a very small chance of creating replication competent virus, steps should still be taken to avoid added risk. The virus is expanded in two rounds of amplification, and all secondary expansions should be performed from an initial expansion stock. Secondary amplifications in HEK293 cells should not be performed from the stock of another secondary expansion, as this could increase the chance of making replication competent virus. See the product manual for more detail and guidelines for screening.

Find additional tips, troubleshooting help, and resources within our RNAi Support Center.

引用和文献 (6)

引用和文献
Abstract
Co-injection of a targeted, reversibly masked endosomolytic polymer dramatically improves the efficacy of cholesterol-conjugated small interfering RNAs in vivo.
Authors:Wong SC, Klein JJ, Hamilton HL, Chu Q, Frey CL, Trubetskoy VS, Hegge J, Wakefield D, Rozema DB, Lewis DL
Journal:Nucleic Acid Ther
PubMed ID:23181701
'Effective in vivo delivery of small interfering (siRNA) has been a major obstacle in the development of RNA interference therapeutics. One of the first attempts to overcome this obstacle utilized intravenous injection of cholesterol-conjugated siRNA (chol-siRNA). Although studies in mice revealed target gene knockdown in the liver, delivery was relatively ... More
Relationship of IL-1 and TNF-a polymorphisms with Helicobacter pylori in gastric diseases in a Brazilian population.
Authors:Santos JC, Ladeira MS, Pedrazzoli J, Ribeiro ML
Journal:Braz J Med Biol Res
PubMed ID:22714811
'It is well known that the risk of development of gastric cancer (GC) in Helicobacter pylori-infected patients depends on several factors. Thus, the aim of this study was to investigate the effect of proinflammatory cytokine gene polymorphisms for IL-1ß, IL-1RN and TNF-a on the development of GC in a Brazilian ... More
Polymorphisms of the TLR2 and TLR4 genes are associated with risk of gastric cancer in a Brazilian population.
Authors:de Oliveira JG, Silva AE
Journal:World J Gastroenterol
PubMed ID:22468087
'To investigate toll-like receptor 2 (TLR2) -196 to -174 del, and TLR4 (+896A/G rs4986790 and +1196C/T rs4986791) polymorphisms at risk of chronic gastritis and gastric cancer in a Brazilian population and association of gastric lesions with risk factors such as smoking, alcohol intake and Helicobacter pylori infection.' ... More
Transcriptome characterization and gene expression of Epinephelus spp in endoplasmic reticulum stress-related pathway during betanodavirus infection in vitro.
Authors:Lu MW, Ngou FH, Chao YM, Lai YS, Chen NY, Lee FY, Chiou PP
Journal:BMC Genomics
PubMed ID:23170826
'Grouper (Epinephelus spp) is an economically important fish species worldwide. However, viral pathogens such as nervous necrosis virus (NNV) have been causing severe infections in the fish, resulting in great loss in the grouper aquaculture industry. Yet, the understanding of the molecular mechanisms underlying the pathogenicity of NNV is still ... More
A non-exothermic cell-embedding tissue-mimicking material for studies of ultrasound-induced hyperthermia and drug release.
Authors:Mylonopoulou E, Bazán-Peregrino M, Arvanitis CD, Coussios CC
Journal:Int J Hyperthermia
PubMed ID:23406389
'The present study aims to create and characterise a cell-embedding tissue-mimicking material (TMM) that has thermal and acoustic properties similar to liver tissue, in order to enable study and optimisation of protocols for ultrasound-induced hyperthermia and drug delivery.' ... More