20 Amino Acids Kit (19 L-amino acids + Glycine)

$395.00

Catalog Number: B2010189 (20 x (1g))
20 Amino Acids Kit (19 L amino acids + Glycine) is a high quality research product used as all-in-one kit of the highly pure 20 natural amino acids (19 L-amino acids plus glycine). This cost-effective kit is useful for screening of amino acids, stabilization of reagents, media formulation, labelling, in vitro synthesis and more. Custom bulk orders of this product are available upon request.

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SKU: B2010189 Categories: ,

Description

20 Amino Acids Kit (19 L amino acids + Glycine)
Catalog number: B2010189
Lot number: Batch Dependent
Expiration Date: Batch dependent
Volume/Weight: 20 x (1g)
pH: na
Supplied as: Ready-to-use
Appearance: Powder of 1 g of each: L-Alanine, L-Arginine, L-Asparagine, L-Aspartic acid, L-Cysteine, L-Cystine, L-Glutamic acid, L-Glutamine, Glycine, L-Histidine , L-Isoleucine, L-Leucine, L-Lysine, L-Methionine, L-Phenylalanine, L-Proline, L-Serine, L-Threonine, L-Tryptophan, L-Tyrosine, L-Valine.
Applications: all-in-one kit of the highly pure 20 natural amino acids (19 L-amino acids plus glycine). This cost-effective kit is useful for screening of amino acids, stabilization of reagents, media formulation, labelling, in vitro synthesis and more.
Storage: Room temperature
Keywords: Amino acids kit, kit of amino acids
Grade: Biotechnology grade. All components are highly pure (minimum 99%). All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered on a 0.22 um.

References:
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2: Jain S, Prajapat G, Abrar M, Ledwani L, Singh A, Agrawal A. Cyanobacteria as
efficient producers of mycosporine-like amino acids. J Basic Microbiol. 2017
Sep;57(9):715-727.

3: Zaia DA, Zaia CT, De Santana H. Which amino acids should be used in prebiotic
chemistry studies? Orig Life Evol Biosph. 2008 Dec;38(6):469-88.

4: Doig AJ. Frozen, but no accident – why the 20 standard amino acids were
selected. FEBS J. 2017 May;284(9):1296-1305.

5: Di Gioia ML, Leggio A, Malagrinò F, Romio E, Siciliano C, Liguori A.
N-Methylated α-Amino Acids And Peptides: Synthesis And Biological Activity. Mini
Rev Med Chem. 2016;16(9):683-90.

6: Grillo MA, Lanza A, Colombatto S. Transport of amino acids through the
placenta and their role. Amino Acids. 2008 May;34(4):517-23.

7: Fichtner M, Voigt K, Schuster S. The tip and hidden part of the iceberg:
Proteinogenic and non-proteinogenic aliphatic amino acids. Biochim Biophys Acta
Gen Subj. 2017 Jan;1861(1 Pt A):3258-3269.

8: de Graaf AJ, Kooijman M, Hennink WE, Mastrobattista E. Nonnatural amino acids
for site-specific protein conjugation. Bioconjug Chem. 2009 Jul;20(7):1281-95.

9: Lelais G, Seebach D. Beta2-amino acids-syntheses, occurrence in natural
products, and components of beta-peptides1,2. Biopolymers. 2004;76(3):206-43.

10: Reddy BS, Chary VN, Pavankumar P, Prabhakar S. Characterization of
N-methylated amino acids by GC-MS after ethyl chloroformate derivatization. J
Mass Spectrom. 2016 Aug;51(8):638-650.

11: Giri C, Goesmann F, Meinert C, Evans AC, Meierhenrich UJ. Synthesis and
chirality of amino acids under interstellar conditions. Top Curr Chem.
2013;333:41-82. doi: 10.1007/128_2012_367.

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