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Glen research/Sulfurizing Reagent II/1kit/40-4037-10

价格
¥1000.00
货号:40-4037-10
浏览量:127
品牌:Glen research
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商品描述
Technical Documents
Description
Details
Dilution/Coupling Data
References
Related Products

Technical Documents

Safety Data Sheet

Sulfurizing Reagent !! - Stable in Solution and Optimized for RNA Sulfurizaion

Safety Data Sheet

Glen Report 18.13: Sulfurizing Reagent II - Stable in Solution and Optimized for RNA Sulfurization

Glen Report 6.23: Research Review - Antisense RNA

Glen Report 18-1 Supplement: Sulfurizing Reagent II and its use in Synthesizing Oligonucleotide Phosphorothioates

Glen Report 4-16: Sulfurization of Oligonucleotides

Glen Report 32-27: Technical Snippets


Description

Sulfurizing Reagent II

Details

Usage

  • Coupling: Sulfurizing: A 60 second sulfurization step time for DNA or a 360 second sulfurization step time for RNA is recommended.Sulfurization step must come before capping step to minimize phosphodiester formation.
  • Deprotection: See TB_Sulfurizing II.pdf
Specifications
Diluent60% pyridine/40% Acetonitrile (fully dissolve in pyridine first, see notes below*)
StorageControlled room temperature or lower, dry
StabilityAt least 6 months

Dilution/Coupling Data

The table below show pack size data and, for solutions, dilution and approximate coupling based on normal priming procedures.

ABI 392/394

Catalog #Pack SizeGrams/Pack0.1M Dil. (mL)Approximate Number of Additions
LV40LV20040nm0.2μm1μm10μm
40-4037-101 g1grams1111111

Expedite

Catalog #Pack SizeGrams/PackDilution (mL)Approximate Number of Additions
Molarity50nm0.2μm1μm15μm
40-4037-101 g1grams111111

References

Literature Highlights

Glen Report 18.1: Sulfurizing Reagent Ii - Stable In Solution And Optimized For Rna Sulfurization
Glen Report 18.1 Supplement: Sulfurizing Reagent Ii And Its Use In Synthesizing Oligonucleotide Phosphorothioates



Glen research表观遗传学是生物学和癌症研究中发展最快的领域之一。虽然基本的遗传密码定义了合成哪些蛋白质和基因产物,但表观遗传控制定义了它们何时何地表达。基因表达的这种动态控制对于X染色体失活,胚胎发生,细胞分化至关重要,并且似乎是记忆形成和突触可塑性的组成部分。在2009年,两份报告1,2  中所述5-羟甲基-2'-脱氧胞苷的发现(HMDC),浦肯野神经元和胚胎干细胞的新颖的DC修饰。后来,第三份报告发现这种修饰在与较高认知功能相关的脑组织中高度丰富。3 dC修饰是通过α-酮戊二酸依赖性十一种11易位(TET)酶的作用产生的,该酶将5-Me-dC氧化为hmdC。这一发现激发了关于可能通过例如碱基切除修复(BER)借助专门的DNA糖基化酶发生的活性脱甲基途径的讨论。或者,可以设想一种方法,其中将hmdC的羟甲基进一步氧化为5-甲酰基-dC(fdC)或5-羧基-dC(cadC),然后消除甲酸或二氧化碳4,5。Glen Research自成立以来就一直为这项研究提供支持,为合成包含所有新dC衍生物-hmdC,fdC和cadC的寡核苷酸提供了基础。第一代hmdC亚磷酰胺已被广泛接受,但需要相当苛刻的脱保护条件。因此,介绍了由Carell和同事开发的与UltraMild脱保护兼容的第二代构建基(5-Hydroxymethyl-dC II)。6  5-甲酰基-dC III旨在满足制备包含所有甲基化变体的寡核苷酸的所有要求。