4-(4-Methylpiperazin-1-ylmethyl)benzoic+acid
Catalog Number:
(102892-790)
Catalog Number:
(10062-464)
Supplier:
Prosci
Description:
16 amino acid peptide near the amino terminus of human SLC27A6.
Supplier:
AMBEED, INC
Description:
Fmoc-Tle-OH 97%
Supplier:
Spectrum Chemicals
Description:
L-Selenomethionine, also known as MSE, is an amino acid containing selenium and readily oxidized. Its ability to deplete reactive oxygen species causes its antioxidant activity.
Supplier:
AMBEED, INC
Description:
Sodium ibandronate 98% (contains <5% H2O)
Supplier:
AMBEED, INC
Description:
5-Aminoisoxazole-4-carboxylic acid ethyl ester 95%
Supplier:
AMBEED, INC
Description:
(R)-5-Amino-2-((tert-butoxycarbonyl)amino)pentanoic acid, Purity: 98%, CAS number: 159877-12-0, Appearance: White to light-yellow powder or crystals, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 5G
Catalog Number:
(10062-364)
Supplier:
Prosci
Description:
18 amino acids near the amino terminus of SPP1.
Supplier:
AMBEED, INC
Description:
(S)-2-Amino-3-(2,5-dichlorophenyl)propanoic acid, Purity: 95%, CAS Number: 754971-91-0, Appearance: White to off-white solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1G
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-β-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 β-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
Supplier:
Enzo Life Sciences
Description:
Microcystins are a group of cyclic heptapeptide hepatotoxins produced by a number of cyanobacterial genera. The most notable of which, and namesake, is the widespread genus Microcystis. Structurally, all microcystins consist of the generalized structure cyclo(-D-Ala1-X2-D-MeAsp3-Y4-Adda5-D-Glu6-Mdha7-). X and Y are variable L-amino acids, D-MeAsp is D-erythro-β-methylaspartic acid and Mdha is N-methyldehydroalanine. Adda is the cyanobacteria unique C20 β-amino acid 3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-deca-4,6-dienoic acid. Substitutions of the variable L-amino acids at positions 2 and 4 give rise to at least 21 known primary microcystin analogs and alterations in the other constituent amino acids result in more than 90 reported mycrocystins to date.
Supplier:
AVANTOR PERFORMANCE MATERIALS US
Description:
Avantor excipients are used during the formulation process in a wide range of applications. Avantor provides high-purity and performance excipients that serve as fillers, binders, disintegrants, lubicants, flavors, emulsifiers and preservatives. All the products are cGMP produced and meet USP grade standards.
Supplier:
ALADDIN SCIENTIFIC
Description:
L-Alanine is a nonessential amino acid that plays a key role in the glucose-alanine cycle between muscle tissue and the liver. In amino acid-degrading tissues such as muscle, amino groups are pooled as glutamate by transamination reactions. The amino group of glutamate is transferred to pyruvate via alanine aminotransferase, forming alanine and α-ketoglutarate. The alanine is passed into the blood and transported to the liver. This reaction is reversed in the liver where pyruvate can be used in gluconeogenesis to form glucose, which may return to other tissues through the circulatory system.A nonessential amino acid that plays a key role in the glucose-alanine cycle
Supplier:
MP Biomedicals
Description:
L-Tryptophan is an amino acid precursor of serotonin and melatonin.
Supplier:
Chemglass
Description:
Vacuum hydrolysis tubes used in protein hydrolysis, amino acid separations, freeze drying or any application under vacuum.
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