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Fig
ure
2.
(
A
) Reversed-phase HPLC pattern on a Primesphere 10 C
18
column of active fraction from Fr IV and HPLC operation was carried out with 15% acetonitrile as mobile phase at 1 mL/min of a flow rate using UV detector at 215 nm. (
B
). Inhibition NO production activities of fractions of Reversed-phase HPLC pattern on a Primesphere 10 C18 column chromatography. Error bars represent mean and S.D from triplicate experiments after deduction of background values from raw values. (
C
) Further separation of active fraction peak responsible for the highest production activity was finally purified on a Synchropak RPP-100 analytical column. HPLC operation was carried out with 10% acetonitrile as mobile phase at 1 mL/min of a flow rate using UV detector at 215 nm. (
D
). Identification of molecular mass and amino acid sequence of AAIP. MS/MS experiments were performed on a Q-TOF tandem mass spectrometer (Micromass Co., Manchester, UK) equipped with a nano-ESI source. Sequencing of active peptide was acquired over the m/z range 50-2500 and sequenced by using the PepSeq de nove sequencing algorithm (Qian et al. (2016))
From
Inhibitory Effects and Molecular Mechanism of an Anti-inflammatory Peptide Isolated from Intestine of Abalone,
Haliotis
D
iscus
H
annai
on LPS-Induced Cytokine Production via the p-p38/p-JNK Pathways in RAW264.7 Macrophages
Zhong-Ji Qian, BoMi Ryu, Won Sun Park, IL-Whan Choi, Won-Kyo Jung
Journal of Food and Nutrition Research
.
2016
, 4(10), 690-698 doi:10.12691/jfnr-4-10-9
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