Examples of 'relevant fractions' in a sentence
Meaning of "relevant fractions"
relevant fractions - This refers to specific parts or components of a whole that are significant or applicable to the current topic or situation
How to use "relevant fractions" in a sentence
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relevant fractions
The relevant fractions were combined and concentrated.
Fractions were analysed by analytical HPLC and MS and relevant fractions were pooled and lyophilised.
The relevant fractions were rotary evaporated to dryness.
The fractions were analysed by A280 and SDS-PAGE and relevant fractions pooled.
Relevant fractions were combined and solvent evaporated in vacuo.
Concentration of the relevant fractions gave a pale yellow solid.
Relevant fractions are combined to give the title compound.
Concentration of the relevant fractions afforded the title compound ( 6.11 g ) as a white solid.
Relevant fractions were combined and the solvent removed.
The relevant fractions were concentrated.
Relevant fractions were concentrated to afford a pale yellow oil.
Collect the relevant fractions containing the title compound and concentrate the fractions.
Relevant fractions were combined and the solvent evaporated.
The relevant fractions were combined and concentrated in vacuo.
The relevant fractions were combined and evaporated to dryness.
See also
Relevant fractions are combined to afford the title compound.
Relevant fractions were lyophilized overnight.
The relevant fractions were collected and solvent removed in vacuo.
The relevant fractions were concentrated in vacuo to give a brown gum.
Relevant fractions were lyophilised.
Relevant fractions were combined.
The relevant fractions were combined and concentrated in vacuo to give an oil.
In the relevant fractions enzyme activity and protein concentration was determined.
The relevant fractions were evaporated under reduced pressure and stirred in ether.
The relevant fractions were concentrated and the residue dissolved in ethyl acetate.
The relevant fractions were concentrated and analysed by LCMS.
The relevant fractions from MDAP were combined and the solvent stripped.
The relevant fractions from MDAP were combined and the solvent evaporated.
Relevant fractions were identified by LCMS and freezedried.
Relevant fractions were pooled, evaporated and lyophilized.
The relevant fractions were combined, concentrated and dried.
The relevant fractions were combined, concentrated and dried in vacuo.
The relevant fractions were pooled and concentrated to provide an off-white solid intermediate.
These relevant fractions can be dialyzed, further purified, and then stored or analyzed.
The relevant fractions were combined and concentrated to provide a red-tan solid intermediate.
The relevant fractions were analysed for 3H content by liquid scintillation counting.
The relevant fractions were combined and concentrated to provide Compound 59 as a white solid.
The relevant fractions were pooled and concentrated to provide Compound 51 as a sticky solid.
The relevant fractions are collected, concentrated in vacuo, and the product is characterised by NMR.
The relevant fractions were collected, concentrated in vacuo, and the product was characterised by NMR.
The relevant fractions were analyzed on a SDS-PAGE gel stained by a standard silver staining protocol.
The relevant fractions containing the IGF1 were analyzed using analytical reverse phase HPLC.
The relevant fractions were combined giving 5.5 g of the desired product.
The relevant fractions were pooled and concentrated to afford the product as a transparent solid ( 52 mg ).
The relevant fractions were evaporated and the residue taken up in diethyl ether ( 20ml ).
Relevant fractions were combined to afford the title compound as a light yellow solid ( 7mg ).
The relevant fractions were combined and concentrated under vacuum to leave yellow oil ( 91 mg ).
The relevant fractions were combined and reduced in vacuo to give a colourless film ( 27mg ).
Relevant fractions were combined to give the desired product ( 47 mg ), after tnturation with a little methanol.
From the relevant fractions 14.7 g pure title compound was obtained after evaporation as a white crystalline solid.
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