Deprecated: Required parameter $cat_id follows optional parameter $type in /data/ebiomall/systems/hong.php on line 2088

Deprecated: Required parameter $where follows optional parameter $tree_id in /data/ebiomall/systems/hlb.php on line 3505
MCLAB/SuperMix (dC)/NGMC-200/1 Ea-蚂蚁淘商城
新闻动态

MCLAB/SuperMix (dC)/NGMC-200/1 Ea

  
  2026-07-31
  
DNA Homopolymeric Tailing Super Mix provides qualified reagents for the addition of homopolymer tails to the 3' ends of DNA with terminal deoxynucleotidyl transferase (TdT).

Description:DNA Homopolymeric Tailing Kit provides qualified reagents for the addition of homopolymer tails to the 3' ends of DNA with terminal deoxynucleotidyl transferase (TdT). Under optimized assay condition, approximately average of 30~70nt oligo(dA) and oligo(dT) or 15~45nt oligo(dC) and oligo(dG) could be added to the target substrate.TdT is a template-independent DNA polymerase that catalyzes the repetitive addition of deoxynucleotides to the 3' hydroxyl terminus of DNA molecules. The enzyme was generated from an E. coli strain that carries the cloned TdT gene from calf thymus with selected mutations. Protruding, recessed or blunt-ended double or single-stranded DNA molecules serve as a substrate for TdT. The addition of dNTPs to 3′-overhanging ends is more efficient than with 3'-recessed or blunt ends. TdT incorporates dATP and dTTP with higher efficiency than dCTP and dGTP. The optimized master mixture stimulates the tailing of the 3'-ends of DNA fragments, even applicable for incorporating ribonucleotides and modified nucleotides (e.g., fluorescein-, biotin-, aminoallyl-labeled nucleotides and dideoxynucleotides).Figures:\"DNAFigure 1: Fragment analysis through 3730 xl DNA Analyzer shows an oligo(dA) tail was added to 5’ fluorescently labeled single strand DNA oligo using DNA Homopolymeric Tailing Master Mix (dA) Kit. Arrow: Tailing reaction final product. A: Fifteen minutes at 37°C reaction product with a 50 nt average length of homopolymer dA tail. B: Thirty minutes at 37°C reaction product with a 65 nt average length of homopolymer dA tail.\"\"Figure 2: Fragment analysis through 3730 xl DNA Analyzer shows an oligo(dC) tail was added to 5’ fluorescently labeled single strand DNA oligo using DNA Homopolymeric Tailing Master Mix (dC) Kit. Arrow: Tailing reaction final product. A: Twenty minutes at 37°C reaction product with a 38 nt average length of homopolymer dC tail. B: Forty minutes at 37°C reaction product with a 45 nt average length of homopolymer dC tail.

 

List of Components:DNA Homopolymeric Tailing Kit is supplied at 2X concentration to allow approximately 50% of the final reaction volume to be used for the addition of substrate solution. Reagents sufficient for 20 or 100 tailing reactions of 10 µL each are provided.DNA Homopolymeric Tailing Kit 20-rxn size:Tailing Enzyme 10ul supplied with 2x:NGMA-100: Master Mix (dA) 100µLNGMT-100: Master Mix (dT) 100µLNGMC-100: Master Mix (dC) 100µLNGMG-100: Master Mix (dG) 100µLDNA Homopolymeric Tailing Kit 100-rxn size:Tailing Enzyme 50ul supplied with 2x:NGMA-200: Master Mix (dA) 500µLNGMT-200: Master Mix (dT) 500µLNGMC-200: Master Mix (dC) 500µLNGMG-200: Master Mix (dG) 500µLComponents:Terminal Deoxynucleotidyl Transferase, Sodium Chloride, Potassium Acetate, Tris-acetate, Magnesium Acetate, Cobalt(II) Chloride and Stabilizers, one of Deoxyadenosine, Deoxythymine, Deoxycytidine and Deoxyguanine. 

Recommended Storage Conditions: DNA Homopolymeric Tailing Kit should be stored at -20°C. The Master Mix should be prevented from light.

References: 1. F. J. Bollum, Terminal deoxynucleotidyl transferase, The Enzymes, the third edition (Boyer, P.D., ed.3, Academic Press, New York, vol.10, 1974) pp. 145-171.2. G. R. Deng, R. Wu, Terminal transferase: Use in the tailing of DNA and for in vitro mutagenesis. Meth. Enzymol. 100, 96-116 (1983).

本文链接: https://www.ebiomall.cn/b377-mclab/info-1562653879.html

免责声明 本文仅代表作者个人观点,与本网无关。其创作性以及文中陈述文字和内容未经本站证实,对本文以及其中全部或者部分内容、文字的真实性、完整性、及时性本站不做任何保证或承诺,请读者仅作参考,并请自行核实相关内容。
版权声明 未经蚂蚁淘授权不得转载、摘编或利用其他方式使用上述作品。已经经本网授权使用作品的,应该授权范围内使用,并注明“来源:蚂蚁淘”。违反上述声明者,本网将追究其相关法律责任。
没有了