Welcome to Sequence Card of Peptide

Details of SAPdb entry with Sequence df

Primary information
SAPdb ID	1309,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Sodium bicarbonate aqueous solution (pH 10)
Method	Appropriate amount of the peptide lipid were dissolved in a sodium bicarbonate aqueous solution (20 mM) by sonication. sample was kept at room temperature to form gel.
Conc	> 1 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Hydogel (Containg Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Hydrogel
	1000
	DF
	N.A.

Primary information
SAPdb ID	1310,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Dichloromethane
Method	Appropriate amounts of the peptide lipid were dissolved in a dichloromethane by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 1.5 wt%
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Nonhelical rigid tape-like structures)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Organogel
	60
	DF
	N.A.

Primary information
SAPdb ID	1311,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Phosphate buffer (pH 7.5)
Method	Appropriate amounts of the peptide lipid were dissolved in a phosphate buffer by sonication. sample was kept at room temperature to form gel.
Conc	> 0.3 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Hydogel (Containg Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Hydrogel
	1000
	DF
	N.A.

Primary information
SAPdb ID	1312,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	1 % NaCl solution
Method	Appropriate amounts of the peptide lipid were dissolved in 1%wt NaCl aqeous solution by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 5 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Nonhelical rigid tape-like structures)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Organogel
	60
	DF
	N.A.

Primary information
SAPdb ID	1313,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Propylen carbonate
Method	Appropriate amounts of the peptide lipid were dissolved in a propylen carbonate by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 0.8 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Nonhelical rigid tape-like structures)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Organogel
	60
	DF
	N.A.

Primary information
SAPdb ID	1314,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Glycerine
Method	Appropriate amounts of the peptide lipid were dissolved in a glycerine by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 3 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Hydogel (Containg Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Hydrogel
	1000
	DF
	N.A.

Primary information
SAPdb ID	1315,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	propylene glycol
Method	Appropriate amounts of the peptide lipid were dissolved in a dichloromethane by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 3 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Nonhelical rigid tape-like structures)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Organogel
	60
	DF
	N.A.

Primary information
SAPdb ID	1316,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	1,3-butanediol
Method	Appropriate amounts of the peptide lipid were dissolved in a propylene glycol by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 3 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Hydogel (Containg Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Hydrogel
	1000
	DF
	N.A.

Primary information
SAPdb ID	1317,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Dimethyl carbonate
Method	Appropriate amounts of the peptide lipid were dissolved in a dimethylcarbonate by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 5 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Nonhelical rigid tape-like structures)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Organogel
	60
	DF
	N.A.

Primary information
SAPdb ID	1318,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Toluene
Method	Appropriate amounts of the peptide lipid were dissolved in a toluene by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 3 wt %
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Organogel (Nonhelical rigid tape-like structures)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Organogel
	60
	DF
	N.A.

Primary information
SAPdb ID	1319,
PMID	23394806
Peptide Name	Aspartame
Peptide sequence	DF
N-Terminal Modification	Free
C-Terminal Modification	Methyl esterification
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide derivative
Technique	(EF - TEM) Energy - Filtering Transmission Electron Microscopy, EF - SEM (Energy - Filtering Scanning Electron Microscopy)
Solvent	Water
Method	Appropriate amounts of the peptide lipid were dissolved in a toluene by sonication. Sodium bicarbonate was used to enhance solubility in water, sample was kept at room temperature to form gel.
Conc	> 1%wt
Temperature	6.8–9.5
Temperature	Room temperature
Incubation Time	12 hours
Year	2013
Self assembly	Yes
Type of Self assembly	Hydrogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	Stable for more than one month
	Hydrogel
	1000
	DF
	N.A.

Primary information
SAPdb ID	1367,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Ethanol
Method	Gelator solution with concentration at 1mg/ml prepared using ethanol as a solvent and incubate for 24 hours at 20°C to form gel.
Conc	1 mg/ml
Temperature	20°C
Incubation Time	1 day
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	DF
	N.A.

Primary information
SAPdb ID	1368,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Ethanol + ultrasonic treatment for 4 minutes
Method	Gelator solution with concentration at 1mg/ml prepared using ethanol as a solvent, followed by ultrasonic treatment for 4 minutes. Finally solution incubated for 24 hours at 20°C to form gel.
Conc	1 mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel (consists of thin and long helical Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	DF
	N.A.

Primary information
SAPdb ID	1369,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Ethanol + quinidine(+) +ultrasonic treatment for 4 minutes
Method	Gelator solution with concentration at 1mg/ml prepared using ethanol as a solvent. To this solution equimolar quinidine(+) added to acclerate the gel formation. Ultrasonic treatment given for 4 minutes. Finally solution incubated for 24 hours at 20°C to form gel.
Conc	1 mg/ml
Temperature	20°C
Incubation Time	30 minutes
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel (consists of wider and thicker helical Nanofibers)
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	DF
	N.A.

Primary information
SAPdb ID	1370,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	df
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Ethanol + quinidine(-) +ultrasonic treatment for 4 minutes
Method	Gelator solution with concentration at 1mg/ml prepared using ethanol as a solvent. To this solution equimolar quinidine(+) added. Ultrasonic treatment given for 4 minutes. Finally solution incubated for 12hours at 20°C to form gel.
Conc	1 mg/ml
Temperature	20°C
Incubation Time	12 hours
Year	2014
Self assembly	No
Type of Self assembly	No organogel formation
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	df
	N.A.

Primary information
SAPdb ID	1372,
PMID	24453207
Peptide Name	G6 or p-Phenyl-L-Ala-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Ethanol
Method	Gelator solution with concentration at 1mg/ml prepared using ethanol as a solvent, followed by ultrasonic treatment for 4 minutes. Finally solution incubated for 24 hours at 20°C to form gel.
Conc	3 mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	DF
	N.A.

Primary information
SAPdb ID	1373,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform
Method	Gelator solution with concentration at 100mg/ml prepared using chloroform as a solvent and then a piece of ultra-flat mica was immersed in the above solution for one hour at 20°C. After that the mica surface was dried by nitrogen flow, and the self-assembled morphology observed.
Conc	100mg/ml
Temperature	20°C
Incubation Time	1 week
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	DF
	N.A.

Primary information
SAPdb ID	1374,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform
Method	Gelator solution with concentration at 0.1mg/ml prepared using chloroform as a solvent and then a piece of ultra-flat mica was immersed in the above solution for one hour at 20°C. After that the mica surface was dried by nitrogen flow, and the self-assembled morphology observed.
Conc	0.1mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Single long fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	DF
	N.A.

Primary information
SAPdb ID	1375,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform
Method	Gelator solution with concentration at 0.5mg/ml prepared using chloroform as a solvent and then a piece of ultra-flat mica was immersed in the above solution for one hour at 20°C. After that the mica surface was dried by nitrogen flow, and the self-assembled morphology observed.
Conc	0.5mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Denditic pattern of fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	DF
	N.A.

Primary information
SAPdb ID	1376,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform
Method	Gelator solution with concentration at 1mg/ml prepared using chloroform as a solvent and then a piece of ultra-flat mica was immersed in the above solution for one hour at 20°C. After that the mica surface was dried by nitrogen flow, and the self-assembled morphology observed.
Conc	1mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Nest like pattern of fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	DF
	N.A.

Primary information
SAPdb ID	1377,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform
Method	Gelator solution with concentration at 2mg/ml prepared using chloroform as a solvent and then a piece of ultra-flat mica was immersed in the above solution for one hour at 20°C. After that the mica surface was dried by nitrogen flow, and the self-assembled morphology observed.
Conc	2mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Nest like pattern of fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	DF
	N.A.

Primary information
SAPdb ID	1378,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform + quinidine(+) +ultrasonic treatment for 4 minutes
Method	Self-assembled morphologies of G1 (1.0 mg·mL-1) mixed with different molar ratios of quinoline in chloroform at 20°C
Conc	1mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Many short fibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	DF
	N.A.

Primary information
SAPdb ID	1379,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform + quinidine(+) +ultrasonic treatment for 4 minutes (ratio 1:1)
Method	Self-assembled morphologies of G1 (1.0 mg·mL-1) mixed with different molar ratios of quinoline in chloroform at 20°C
Conc	1mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	No
Type of Self assembly	No gel formation
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	None
	NA
	DF
	N.A.

Primary information
SAPdb ID	1380,
PMID	24453207
Peptide Name	G1 or p-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform + quinidine(-) +ultrasonic treatment for 4 minutes
Method	Self-assembled morphologies of G1 (1.0 mg·mL-1) mixed with different molar ratios of quinoline in chloroform at 20°C
Conc	1mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Rootlike pattern of Nanofibers
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Nanofibers
	NA
	DF
	N.A.

Primary information
SAPdb ID	1381,
PMID	24453207
Peptide Name	G7 or mono-Phenyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	Mono-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform + quinidine(-) +ultrasonic treatment for 4 minutes
Method	Self-assembled morphologies of G1 (1.0 mg·mL-1) mixed with different molar ratios of quinoline in chloroform at 20°C
Conc	1mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	DF
	N.A.

Primary information
SAPdb ID	1382,
PMID	24453207
Peptide Name	G8 or p-propyl-L-Asp-L-Phe
Peptide sequence	DF
N-Terminal Modification	para-Phenylation
C-Terminal Modification	Free
Non-Terminal Modification	None
Length	2
Peptide/Conjuagate	Peptide
Technique	SEM (Scanning Electron Microscopy), AFM (Atomic Force Microscopy)
Solvent	Chloroform + ethanol +ultrasonic treatment for 4 minutes
Method	Self-assembled morphologies of G1 (1.0 mg·mL-1) mixed with different molar ratios of quinoline in chloroform at 20°C
Conc	1mg/ml
Temperature	20°C
Incubation Time	1hour
Year	2014
Self assembly	Yes
Type of Self assembly	Organogel
Tertiary Structure (Technique)	Not Predicted),
	Linear
	NA
	NA
	Organogel
	NA
	DF
	N.A.