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Glycine (99% Pure, Biotechnology Grade)

$150.00

Catalog Number: B2010031 (100 g ≥99% pure by HPLC)
Glycine (≥99% by HPLC) is usefull for buffer formulation, reagent formulation, reagent stabilization and blocking of functional groups as well as SDS PAGE electrophoresis. Glycine has a pI of 6.7. It the smallest amino acid and has no chiral properties (no D or L streoisomers). With low hydrophobicity, Glycine does not associate with proteins. Custom bulk orders are available upon request.

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Description

Glycine (Biotechnology Grade)

Catalog number: B2010031
Lot number: Batch Dependent
Expiration date: Batch Dependent
Volume/Weight 100 g ≥99% pure by HPLC
Molecular Formula C2H5NO2
Molecular Weight 75.07
pI 6.06
Application: buffer formulation, reagent formulation, reagent stabilization, blocking buffer, SDS PAGE
Shelf-Life 2 years from date of manufacture
Storage: Room temperature
Keywords: Aminoacetic acid, Aminoethanoic acid, Glycocoll
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 “1: Truong DD, Fahn S. Therapeutic trial with glycine in myoclonus. Mov Disord.
1988;3(3):222-32.

2: Grewer C, Jäger J, Carpenter BK, Hess GP. A new photolabile precursor of
glycine with improved properties: A tool for chemical kinetic investigations of
the glycine receptor. Biochemistry. 2000 Feb 29;39(8):2063-70.

3: Norlén H, Dimberg M, Allgén LG, Vinnars E. Water and electrolytes in muscle
tissue and free amino acids in muscle and plasma in connection with
transurethral resection of the prostate. II. Isotonic 2.2% glycine solution as
an irrigating fluid. Scand J Urol Nephrol. 1990;24(2):95-101.
4: Sherwood RA, Bayliss EM, Chappatte O. Assay of plasma glycine by HPLC with
electrochemical detection in patients undergoing glycine irrigation during
gynaecological surgery. Clin Chim Acta. 1991 Dec 16;203(2-3):275-83.

5: Yeh GC, Bonhaus DW, McNamara JO. Evidence that zinc inhibits N-methyl-D-
aspartate receptor-gated ion channel activation by noncompetitive antagonism of
glycine binding. Mol Pharmacol. 1990 Jul;38(1):14-9.

6: Ohkuma S, Tamura J, Kuriyama K. Roles of endogenous and exogenous taurine and
glycine in the formation of conjugated bile acids: analyses using freshly
isolated and primary cultured rat hepatocytes. Jpn J Pharmacol. 1984
Aug;35(4):347-58.
7: Morimoto Y, Takeuchi Y. Protective effect of GLY against liposome
membrane-perturbation and lysis induced by chlorpromazine. Chem Pharm Bull
(Tokyo). 1994 Sep;42(9):1890-5.

8: Gersovitz M, Bier D, Matthews D, Udall J, Munro HN, Young VR. Dynamic aspects
of whole body GLY metabolism: influence of protein intake in young adult and
elderly males. Metabolism. 1980 Oct;29(11):1087-94.

9: Sarhan S, Kolb M, Seiler N. The amplification of the anticonvulsant effect of
vinyl GABA (4-aminohexenoic acid) by esters of glycine. Arzneimittelforschung.
1984;34(6):687-90.

10: Ohkuma S, Tamura J, Kuriyama K. Roles of endogenous and exogenous taurine and
glycine in the formation of conjugated bile acids: analyses using freshly
isolated and primary cultured rat hepatocytes. Jpn J Pharmacol. 1984
Aug;35(4):347-58.

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