MagaDye 561ddATP 货号17062-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

  • 产品参数
  • 产品详情

MagaDye 561ddATP  货号17062
级别 :
超纯、高纯
含量 :
95%
品牌 :
AAT Bioquest
用途范围 :
AAT Bioquest生产的荧光染料
特色服务 :
包邮

产品详情

Product details

MagaDye 561-ddATP

MagaDye 561ddATP  货号17062

简要概述

产品基本信息

货号:17062

产品名称:MagaDye 561-ddATP

规格:5nmoles

储存条件:保存在冰箱-15℃干燥

保质期:12个月

产品物理化学光谱特性

Ex(nm):498

Em(nm):561

吸收(nm):498

  
产品介绍

Sanger测序,也称为链终止法,是一种基于DNA聚合酶选择性掺入链终止双脱氧核苷酸(ddNTPs)的DNA测序技术。虽然新的NGS技术由于其较高的通量能力和较低的每份样品成本而在临床研究实验室中变得很普遍,但Sanger测序仍具有99.99%的准确度。四种不同的荧光ddNTP(标记为BigDye®,BigDye®是ThermoFisher的商标)是执行Sanger测序的关键成分。MagaDye 561-ddATP等同于BigDye dROX,具有几乎相同的光谱。金畔生物是AAT Bioquest的中国代理商,为您提供优质的MagaDye 561-ddATP。 

ddATP 货号17209-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

  • 产品参数
  • 产品详情

ddATP 货号17209
级别 :
超纯、高纯
含量 :
95%
产品规格 :
1 umole
品牌 :
AAT Bioquest
用途范围 :
科研试剂
特色服务 :
包邮

产品详情

Product details

ddATP [2',3'-Dideoxyadenosine-5'-triphosphate]

ddATP 货号17209 货号 17209 存储条件 在零下15度以下保存, 避免光照
规格 1 umole
Ex (nm) Em (nm)
分子量 475.18 溶剂 Water
产品详细介绍

简要概述

产品基本信息

货号:17209

产品名称:ddTTP [2',3'-Dideoxythymidine-5'-triphosphate]

规格:1 umole

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:475.18

溶剂:水

 

产品介绍

Sanger测序,也称为链终止法,是一种基于DNA聚合酶选择性掺入链终止双脱氧核苷酸(ddNTPs)的DNA测序技术。它是由Frederick Sanger及其同事于1977年开发的。尽管新的NGS技术由于其较高的通量能力和较低的每份样品成本而在临床研究实验室中变得很普遍,但Sanger测序的准确度仍为99.99%,仍然是临床的“黄金标准”研究排序。 dd-ATP是执行Sanger测序的四个关键ddNTP组件之一。

2-Aminoethoxypropargyl ddATP 货号17084-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

2-Aminoethoxypropargyl ddATP

2-Aminoethoxypropargyl ddATP

2-Aminoethoxypropargyl ddATP    货号17084 货号 17084 存储条件 在零下15度以下保存, 避免光照
规格 1 umoles 价格 11988
Ex (nm) Em (nm)
分子量 659.24 溶剂 DMF
产品详细介绍

简要概述

产品基本信息

货号:17084

产品名称:2-Aminoethoxypropargyl ddATP

规格:1 umoles

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:659.24

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测序中最早最靠谱的方法之一,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最后的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,片段的长度从最长到最短分离,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。金畔生物是AAT Bioquest的中国代理商,为您提供最优质的2-Aminoethoxypropargyl ddATP。 

 

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

说明书
2-Aminoethoxypropargyl ddATP.pdf

MagaDye 561-ddATP 货号17062-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

MagaDye 561-ddATP

MagaDye 561-ddATP

MagaDye 561-ddATP    货号17062 货号 17062 存储条件 在零下15度以下保存, 避免光照
规格 5 nmoles 价格 11988
Ex (nm) 498 Em (nm) 561
分子量 ~2000 溶剂 Water
产品详细介绍

简要概述

产品基本信息

货号:17062

产品名称:MagaDye 561-ddATP

规格:5nmoles

储存条件:保存在冰箱-15℃干燥

保质期:12个月

 

产品物理化学光谱特性

Ex(nm):498

Em(nm):561

吸收(nm):498

  
产品介绍

Sanger测序,也称为链终止法,是一种基于DNA聚合酶选择性掺入链终止双脱氧核苷酸(ddNTPs)的DNA测序技术。虽然新的NGS技术由于其较高的通量能力和较低的每份样品成本而在临床研究实验室中变得很普遍,但Sanger测序仍具有99.99%的准确度。四种不同的荧光ddNTP(标记为BigDye®,BigDye®是ThermoFisher的商标)是执行Sanger测序的关键成分。MagaDye 561-ddATP等同于BigDye dROX,具有几乎相同的光谱。金畔生物是AAT Bioquest的中国代理商,为您提供最优质的MagaDye 561-ddATP。 

点击查看光谱

 

参考文献

A novel gross deletion and breakpoint junction sequence analysis of ATP7B in a Chinese family with Wilson disease using next‑generation sequencing and Sanger sequencing.
Authors: Liu, Wei-Liang and Li, Fang and Liu, Lu and Chen, Wei and He, Zhi-Xu and Gu, Hao and Ai, Rong
Journal: Molecular medicine reports (2020): 517-523

Concurrent Cultivation of Mycobacterium avium and Mycobacterium intracellulare Identified by a Single Sanger Sequencing of the 16S Gene.
Authors: Han, Xiang Y and Golshan, Mohammad A and Bowman, Christopher J
Journal: Journal of clinical microbiology (2020)

Detection of TERT promoter mutation in serum cell-free DNA using wild-type blocking PCR combined with Sanger sequencing in hepatocellular carcinoma.
Authors: Akuta, Norio and Suzuki, Fumitaka and Kobayashi, Mariko and Fujiyama, Shunichiro and Kawamura, Yusuke and Sezaki, Hitomi and Hosaka, Tetsuya and Kobayashi, Masahiro and Saitoh, Satoshi and Arase, Yasuji and Ikeda, Kenji and Suzuki, Yoshiyuki and Kumada, Hiromitsu
Journal: Journal of medical virology (2020)

Guidelines for Sanger sequencing and molecular assay monitoring.
Authors: Crossley, Beate M and Bai, Jianfa and Glaser, Amy and Maes, Roger and Porter, Elizabeth and Killian, Mary Lea and Clement, Travis and Toohey-Kurth, Kathy
Journal: Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc (2020): 1040638720905833

Rapid, Inexpensive Measurement of Synthetic Bacterial Community Composition by Sanger Sequencing of Amplicon Mixtures.
Authors: Cermak, Nathan and Datta, Manoshi Sen and Conwill, Arolyn
Journal: iScience (2020): 100915

Shall I trust the report? Variable performance of Sanger sequencing revealed by deep sequencing on HIV drug resistance mutation detection.
Authors: Chen, Nan-Yu and Kao, Shu-Wei and Liu, Zhuo-Hao and Wu, Ting-Shu and Tsai, Chia-Lung and Lin, Hsi-Hsun and Wong, Wing-Wai and Chang, Yea-Yuan and Chen, Shu-Sheng and Ku, Stephane Wen-Wei
Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases (2020): 182-191

Update on molecular companion diagnostics – a future in personalized medicine beyond Sanger sequencing.
Authors: Campbell, Michelle Renee
Journal: Expert review of molecular diagnostics (2020)

BEAT: A Python Program to Quantify Base Editing from Sanger Sequencing.
Authors: Xu, Li and Liu, Yakun and Han, Renzhi
Journal: The CRISPR journal (2019): 223-229

Characterization and Clinical Significance of Natural Variability in Hepatitis B Virus Reverse Transcriptase in Treatment-Naive Chinese Patients by Sanger Sequencing and Next-Generation Sequencing.
Authors: Fu, Ya and Zeng, Yongbin and Chen, Tianbin and Chen, Huijuan and Lin, Ni and Lin, Jinpiao and Liu, Xiaofeng and Huang, Er and Wu, Songhang and Wu, Shu and Xu, Siyi and Wang, Long and Ou, Qishui
Journal: Journal of clinical microbiology (2019)

Comparison of Sanger sequencing for hepatitis C virus genotyping with a commercial line probe assay in a tertiary hospital.
Authors: Goletti, Sylvie and Zuyten, Siméon and Goeminne, Léonie and Verhofstede, Chris and Rodriguez-Villalobos, Hector and Bodeus, Monique and Stärkel, Peter and Horsmans, Yves and Kabamba-Mukadi, Benoît
Journal: BMC infectious diseases (2019): 738

说明书
MagaDye 561-ddATP.pdf

MagaDye™ 561-ddATP 货号17066-AAT Bioquest荧光染料

上海金畔生物科技有限公司代理AAT Bioquest荧光染料全线产品,欢迎访问AAT Bioquest荧光染料官网了解更多信息。

MagaDye™ 561-ddATP

MagaDye™ 561-ddATP

MagaDye™ 561-ddATP    货号17066 货号 17066 存储条件
规格 50 nmoles 价格 62412
Ex (nm) 498 Em (nm) 561
分子量 ~2000 溶剂
产品详细介绍

简要概述

产品基本信息

货号:17066

产品名称:MagaDye 561-ddATP

规格:50nmoles

储存条件:保存在冰箱-15℃干燥

保质期:12个月

 

产品物理化学光谱特性

Ex(nm):498

Em(nm):561

吸收(nm):498

  
产品介绍

Sanger测序,也称为链终止法,是一种基于DNA聚合酶选择性掺入链终止双脱氧核苷酸(ddNTPs)的DNA测序技术。虽然新的NGS技术由于其较高的通量能力和较低的每份样品成本而在临床研究实验室中变得很普遍,但Sanger测序仍具有99.99%的准确度。四种不同的荧光ddNTP(标记为BigDye®,BigDye®是ThermoFisher的商标)是执行Sanger测序的关键成分。MagaDye 561-ddATP等同于BigDye dROX,具有几乎相同的光谱。金畔生物是AAT Bioquest的中国代理商,为您提供最优质的MagaDye 561-ddATP。 

点击查看光谱

 

参考文献

A novel gross deletion and breakpoint junction sequence analysis of ATP7B in a Chinese family with Wilson disease using next‑generation sequencing and Sanger sequencing.
Authors: Liu, Wei-Liang and Li, Fang and Liu, Lu and Chen, Wei and He, Zhi-Xu and Gu, Hao and Ai, Rong
Journal: Molecular medicine reports (2020): 517-523

Concurrent Cultivation of Mycobacterium avium and Mycobacterium intracellulare Identified by a Single Sanger Sequencing of the 16S Gene.
Authors: Han, Xiang Y and Golshan, Mohammad A and Bowman, Christopher J
Journal: Journal of clinical microbiology (2020)

Detection of TERT promoter mutation in serum cell-free DNA using wild-type blocking PCR combined with Sanger sequencing in hepatocellular carcinoma.
Authors: Akuta, Norio and Suzuki, Fumitaka and Kobayashi, Mariko and Fujiyama, Shunichiro and Kawamura, Yusuke and Sezaki, Hitomi and Hosaka, Tetsuya and Kobayashi, Masahiro and Saitoh, Satoshi and Arase, Yasuji and Ikeda, Kenji and Suzuki, Yoshiyuki and Kumada, Hiromitsu
Journal: Journal of medical virology (2020)

Guidelines for Sanger sequencing and molecular assay monitoring.
Authors: Crossley, Beate M and Bai, Jianfa and Glaser, Amy and Maes, Roger and Porter, Elizabeth and Killian, Mary Lea and Clement, Travis and Toohey-Kurth, Kathy
Journal: Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc (2020): 1040638720905833

Rapid, Inexpensive Measurement of Synthetic Bacterial Community Composition by Sanger Sequencing of Amplicon Mixtures.
Authors: Cermak, Nathan and Datta, Manoshi Sen and Conwill, Arolyn
Journal: iScience (2020): 100915

Shall I trust the report? Variable performance of Sanger sequencing revealed by deep sequencing on HIV drug resistance mutation detection.
Authors: Chen, Nan-Yu and Kao, Shu-Wei and Liu, Zhuo-Hao and Wu, Ting-Shu and Tsai, Chia-Lung and Lin, Hsi-Hsun and Wong, Wing-Wai and Chang, Yea-Yuan and Chen, Shu-Sheng and Ku, Stephane Wen-Wei
Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases (2020): 182-191

Update on molecular companion diagnostics – a future in personalized medicine beyond Sanger sequencing.
Authors: Campbell, Michelle Renee
Journal: Expert review of molecular diagnostics (2020)

BEAT: A Python Program to Quantify Base Editing from Sanger Sequencing.
Authors: Xu, Li and Liu, Yakun and Han, Renzhi
Journal: The CRISPR journal (2019): 223-229

Characterization and Clinical Significance of Natural Variability in Hepatitis B Virus Reverse Transcriptase in Treatment-Naive Chinese Patients by Sanger Sequencing and Next-Generation Sequencing.
Authors: Fu, Ya and Zeng, Yongbin and Chen, Tianbin and Chen, Huijuan and Lin, Ni and Lin, Jinpiao and Liu, Xiaofeng and Huang, Er and Wu, Songhang and Wu, Shu and Xu, Siyi and Wang, Long and Ou, Qishui
Journal: Journal of clinical microbiology (2019)

Comparison of Sanger sequencing for hepatitis C virus genotyping with a commercial line probe assay in a tertiary hospital.
Authors: Goletti, Sylvie and Zuyten, Siméon and Goeminne, Léonie and Verhofstede, Chris and Rodriguez-Villalobos, Hector and Bodeus, Monique and Stärkel, Peter and Horsmans, Yves and Kabamba-Mukadi, Benoît
Journal: BMC infectious diseases (2019): 738

说明书
MagaDye™ 561-ddATP.pdf