Search
Citations & References (5)
Invitrogen™
Alexa Fluor™ 555-aha-dUTP, 1 mM in TE buffer
Labeled 5-aminohexylacrylamido-dUTP (aha-dUTP) nucleotides are modified at the C-5 position of uridine with a unique hexylacrylamide linker, which serves asRead more
| Catalog Number | Quantity |
|---|---|
| A32762 | 50 μL |
Catalog number A32762
Price (KRW)
1,020,000
Each
Quantity:
50 μL
Price (KRW)
1,020,000
Each
Labeled 5-aminohexylacrylamido-dUTP (aha-dUTP) nucleotides are modified at the C-5 position of uridine with a unique hexylacrylamide linker, which serves as a spacer between the nucleotide and the dye. This spacer reduces interactions between the nucleotide and the dye, resulting in brighter conjugates and increased hapten accessibility for secondary detection reagents. Labeled nucleotides can be used to generate labeled nucleic acid hybridization probes for many molecular biology and molecular cytogenetics applications, including multicolor techniques.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Concentration1 mM
For Use With (Application)Molecular Biology
Label or DyeAlexa Fluor Dye
ModificationAHA (5-aminohexylacrylamido)
Product LineAlexa Fluor
Product TypeLabeled Nucleotide
Quantity50 μL
Shipping ConditionWet Ice
Unit SizeEach
Contents & Storage
Store in freezer (-5 to -30°C) and protect from light.
Frequently asked questions (FAQs)
Can dU-containing DNA produced by amplification with dUTP be cut by restriction enzymes?
Citations & References (5)
Citations & References
Abstract
Transcriptome for photobiological hydrogen production induced by sulfur deprivation in the green alga Chlamydomonas reinhardtii.
Journal:Eukaryot Cell
PubMed ID:18708561
'Photobiological hydrogen production using microalgae is being developed into a promising clean fuel stream for the future. In this study, microarray analyses were used to obtain global expression profiles of mRNA abundance in the green alga Chlamydomonas reinhardtii at different time points before the onset and during the course of
Effects of nitroglycerin or pentaerithrityl tetranitrate treatment on the gene expression in rat hearts: evidence for cardiotoxic and cardioprotective effects.
Journal:Physiol Genomics
PubMed ID:19417013
Nitroglycerin (NTG) and pentaerithrityl tetranitrate (PETN) are organic nitrates used in the treatment of angina pectoris, myocardial infarction, and congestive heart failure. Recent data show marked differences in the effects of NTG and PETN on the generation of reactive oxygen species. These differences are attributed to different effects of NTG
Transcriptomic signatures of alterations in a myoblast cell line infected with four distinct strains of Trypanosoma cruzi.
Journal:Am J Trop Med Hyg
PubMed ID:20439965
We examined the extent to which different Trypanosoma cruzi strains induce transcriptomic changes in cultured L(6)E(9) myoblasts 72 hours after infection with Brazil (TC I), Y (TC II), CL (TC II), and Tulahuen (TC II) strains. Expression of 6,289 distinct, fully annotated unigenes was quantified with 27,000 rat oligonucleotide arrays
Abnormal distribution of inositol 1,4,5-trisphosphate receptors in human muscle can be related to altered calcium signals and gene expression in Duchenne dystrophy-derived cells.
Journal:FASEB J
PubMed ID:20395455
Inositol 1,4,5-trisphosphate (IP(3)) receptors (IP(3)Rs) drive calcium signals involved in skeletal muscle excitation-transcription coupling and plasticity; IP(3)R subtype distribution and downstream events evoked by their activation have not been studied in human muscle nor has their possible alteration in Duchenne muscular dystrophy (DMD). We studied the expression and localization of
A novel multiple FISH array for the detection of genetic aberrations in cancer.
Journal:Lab Invest
PubMed ID:16518404
Interphase multicolor fluorescence in situ hybridization (IM-FISH) has great promise for improving cancer diagnosis because it can directly visualize multiple changes in chromosomes and gene copy number on a cell-to-cell basis. However, no more than four targets can be detected simultaneously by current commercially available IM-FISH protocols, and the DNA