Catalogue Number
BN-O0974
Analysis Method
HPLC,NMR,MS
Specification
98%(HPLC)
Storage
2-8°C
Molecular Weight
329.39
Appearance
Powder
Botanical Source
Structure Type
Alkaloids
Category
Standards;Natural Pytochemical;API
SMILES
CCC(=O)C1=CC=C(C=C1)OCC2=CC=C(C=C2)C3=CC=CC=C3C#N
Synonyms
2-[4-[(4-propanoylphenoxy)methyl]phenyl]benzonitrile
IUPAC Name
3-[(2S,4S)-2,4-dimethylhexanoyl]-4-hydroxy-5-(4-hydroxyphenyl)-1H-pyridin-2-one
Density
Solubility
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Flash Point
Boiling Point
Melting Point
InChl
InChI=1S/C23H19NO2/c1-2-23(25)19-11-13-21(14-12-19)26-16-17-7-9-18(10-8-17)22-6-4-3-5-20(22)15-24/h3-14H,2,16H2,1H3
InChl Key
QMZOHTUVRXCUCH-UHFFFAOYSA-N
WGK Germany
RID/ADR
HS Code Reference
2933990000
Personal Projective Equipment
Correct Usage
For Reference Standard and R&D, Not for Human Use Directly.
Meta Tag
provides coniferyl ferulate(CAS#:935863-26-6) MSDS, density, melting point, boiling point, structure, formula, molecular weight etc. Articles of coniferyl ferulate are included as well.>> amp version: coniferyl ferulate
No Technical Documents Available For This Product.
21573114
RNA Seq provides unparalleled levels of information about the transcriptome including precise expression levels over a wide dynamic range. It is essential to understand how technical variation impacts the quality and interpretability of results, how potential errors could be introduced by the protocol, how the source of RNA affects transcript detection, and how all of these variations can impact the conclusions drawn. Multiple human RNA samples were used to assess RNA fragmentation, RNA fractionation, cDNA synthesis, and single versus multiple tag counting. Though protocols employing polyA RNA selection generate the highest number of non-ribosomal reads and the most precise measurements for coding transcripts, such protocols were found to detect only a fraction of the non-ribosomal RNA in human cells. PolyA RNA excludes thousands of annotated and even more unannotated transcripts, resulting in an incomplete view of the transcriptome. Ribosomal-depleted RNA provides a more cost-effective method for generating complete transcriptome coverage. Expression measurements using single tag counting provided advantages for assessing gene expression and for detecting short RNAs relative to multi-read protocols. Detection of short RNAs was also hampered by RNA fragmentation. Thus, this work will help researchers choose from among a range of options when analyzing gene expression, each with its own advantages and disadvantages.
Protocol Dependence of Sequencing-Based Gene Expression Measurements
Tal Raz, Philipp Kapranov, Doron Lipson, Stan Letovsky, Patrice M. Milos, and John F. Thompson * Najib M. El-Sayed, Editor
2011;
Description :
Empty ...