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Aminopropargyl ddCTP [5-Propargylamino-2',3'-dideoxycytidine-5'-triphosphate]

英文名称:Aminopropargyl ddCTP [5-Propargylamino-2',3'-dideoxycytidine-5'-triphosphate]
Aminopropargyl ddCTP [5-Propargylamino-2',3'-dideoxycytidine-5'-triphosphate]
价格 12950
产品规格
10 umoles

产品货号
产品参数
Ex (nm)-Em (nm)-
分子量592.15溶剂DMF
存储条件在零下15度以下保存, 避免光照
产品概述

产品基本信息

产品名称:Aminopropargyl ddCTP [5-Propargylamino-2',3'-dideoxycytidine-5'-triphosphate]

CAS:114748-56-0

储存条件:-15℃避光防潮

保质期:24个月

 

产品物理化学光谱特性

分子量:592.15

外观:液体

溶剂:DMF

激发波长(nm):N/A

发射波长(nm):N/A

 

产品介绍

Sanger法是DNA测序中早靠谱的方法之一,DNA由四种脱氧核苷酸三磷酸(dNTP)合成。将每个新核苷酸添加到后的dNTP的3'-OH基团中。可以将二脱氧胸苷三磷酸(ddTTPs)添加到正在生长的DNA链中,但是当它出现时,链延长会停止,因为下一个要连接的核苷酸没有3'-OH。待测序的DNA被制备成单链。该模板DNA带有大量dATP,dGTP,dCTP和dTTP的混合物。加入四种双脱氧核苷酸(ddATP,ddGTP,ddCTP和ddTTP)的混合物,每种混合物均以限量存在,并分别用发不同颜色的荧光的“标签​​”标记。因为所有四个正常核苷酸都存在,所以链延伸正常进行,直到偶然地DNA聚合酶插入ddNTP(而不是正常dNTP)。如果正常核苷酸与双脱氧形式的比率足够高,则在插入ddNTP之前,某些DNA链将成功添加数百个核苷酸,从而终止该过程。在孵育期结束时,片段的长度从长到短分离,一个核苷酸之间的差异足以使该链与下一较短和下一较长链分开。当被激光束照射时,四个DDNTP中的每一个都会发出不同的荧光,可以通过自动扫描仪打印输出序列。这些ddATP,ddGTP,ddCTP和ddTTP胺衍生物是开发Sanger测序试剂的重要组成部分。百萤生物是AAT Bioquest的中国代理商,为您提供优质的Aminopropargyl ddCTP [5-Propargylamino-2',3'-dideoxycytidine-5'-triphosphate]。 

 

参考文献

Polyadenylated sequencing primers enable complete readability of PCR amplicons analyzed by dideoxynucleotide sequencing
Authors: Beranek, M., Drastikova, M., Petera, J.
Journal: Acta Medica (Hradec Kralove) (2012): 160-4

UV-induced bond modifications in thymine and thymine dideoxynucleotide: structural elucidation of isomers by differential mobility mass spectrometry
Authors: St-Jacques, A., Anichina, J., Schneider, B. B., Covey, T. R., Bohme, D. K.
Journal: Anal Chem (2010): 6163-7

Analysis of processivity of mungbean dideoxynucleotide-sensitive DNA polymerase and detection of the activity and expression of the enzyme in the meristematic and meiotic tissues and following DNA damaging agent
Authors: Roy, S., Choudhury, S. R., Sengupta, D. N.
Journal: Arch Biochem Biophys (2008): 55-65

A dideoxynucleotide-sensitive DNA polymerase activity characterized from endoreduplicating cells of mungbean (Vigna radiata L.) during ontogeny of cotyledons
Authors: Roy, S., Sarkar, S. N., Singh, S. K., Sengupta, D. N.
Journal: FEBS J (2007): 2005-23

Mechanism-based suppression of dideoxynucleotide resistance by K65R human immunodeficiency virus reverse transcriptase using an alpha-boranophosphate nucleoside analogue
Authors: Selmi, B., Boretto, J., Sarfati, S. R., Guerreiro, C., Canard, B.
Journal: J Biol Chem (2001): 48466-72

Synthesis of the first ferrocene-labeled dideoxynucleotide and its use for 3'-redox end-labeling of 5'-modified single-stranded oligonucleotides
Authors: Anne, A., Blanc, B., Moiroux, J.
Journal: Bioconjug Chem (2001): 396-405

Improving dideoxynucleotide-triphosphate utilisation by the hyper-thermophilic DNA polymerase from the archaeon Pyrococcus furiosus
Authors: Evans, S. J., Fogg, M. J., Mamone, A., Davis, M., Pearl, L. H., Connolly, B. A.
Journal: Nucleic Acids Res (2000): 1059-66

Structure-based design of Taq DNA polymerases with improved properties of dideoxynucleotide incorporation
Authors: Li, Y., Mitaxov, V., Waksman, G.
Journal: Proc Natl Acad Sci U S A (1999): 9491-6

Characterization of the native and recombinant catalytic subunit of human DNA polymerase gamma: identification of residues critical for exonuclease activity and dideoxynucleotide sensitivity
Authors: Longley, M. J., Ropp, P. A., Lim, S. E., Copel and W. C.
Journal: Biochemistry (1998): 10529-39

Comparative performance of high-density oligonucleotide sequencing and dideoxynucleotide sequencing of HIV type 1 pol from clinical samples
Authors: Gunthard, H. F., Wong, J. K., Ignacio, C. C., Havlir, D. V., Richman, D. D.
Journal: AIDS Res Hum Retroviruses (1998): 869-76