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Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO

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产品名称: Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO
产品型号: 21050
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Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO 21050


Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO  的详细介绍

Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO

Click chemistry
Cat. # Quantity Price Lead time
21050 1.5 mL  55.00$ in stock
 
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Copper (II)-TBTA complex is a component of catalyst used for Click Chemistry conjugation reaction. Actual catalyst contains Cu(I), but this reagent cannot be stored, and should be generated from Copper(II)-TBTA complex in situ by reduction. To activate this catalyst, reductant such as ascorbic acid should be added to reaction mixture.

Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO
Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO
Copper(II)-TBTA complex, 10 mM in 55% aq. DMSO
Copper(II)-TBTA complex structure
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Recommended protocol

Click-Chemistry Labeling of Oligonucleotides and DNA

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General properties

Appearance: blue solution
Molecular weight: 690.23
Molecular formula: C30H30CuN10O4S
Quality control: functional testing (Click Chemistry)
Storage conditions: Storage: 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks.
MSDS: Download

Product citations

  1. Routh, A.; Ji, P.; Jaworski, E.; Xia, Z.; Li, W.; Wagner, E.J. Poly(A)-ClickSeq: click-chemistry for next-generation 3′-end sequencing without RNA enrichment or fragmentation. Nucleic Acids Research, 2017, 45(12), e112. doi: 10.1093/nar/gkx286
  2. Jaworski, E.; Routh, A. Parallel ClickSeq and Nanopore sequencing elucidates the rapid evolution of defective-interfering RNAs in Flock House virus. PLOS Pathogens, 2017, 13(5), e1006365. doi: 10.1371/journal.ppat.1006365
  3. Taskova, M.; Uhd, J.; Miotke, L.; Kubit, M.; Bell, J.; Ji, H.P.; Astakhova, K. Tandem Oligonucleotide Probe Annealing and Elongation To Discriminate Viral Sequence. Analytical Chemistry, 2017, 89(8), 4363–4366. doi: 10.1021/acs.analchem.7b00646
  4. Taskova, M.; Madsen, C.S.; Jensen, K.J.; Hansen, L.H.; Vester, B.; Astakhova, K. Antisense oligonucleotides internally labeled with peptides show improved target recognition and stability to enzymatic degradation. Bioconjugate Chemistry, 2017, 28(3), 768–774. doi: 10.1021/acs.bioconjchem.6b00567
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