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G3171

Sigma-Aldrich

Glycinin from Glycine max (soybean)

soybean storage protein

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About This Item

UNSPSC Code:
12352202
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biological source

Glycine max (soybean)

assay

≥80% (HPLC)

form

lyophilized powder

UniProt accession no.

P02858
P04347
P04405
P04776
P11828

storage temp.

−20°C

Gene Information

soybean ... GY1(547901) , GY2(547900) , GY3(547463) , GY4(100101841) , GY5(547452)

General description

Glycinins are a family of soybean storage proteins produced during embryogenesis. Glycinin is a major allergen within soy and is a soluble glycoprotein that exists in a homo-hexameric form. At least five genes encode for the most abundant subunits.
Naturally occuring mixture of glycinin isoforms

Biochem/physiol Actions

Glycinin is a hexameric protein containing six similar subunits, each of which comprises an acidic polypeptide chain connected by disulfide bonds to a basic polypeptide chain.[1]

pictograms

Health hazard
GHS08

signalword

Danger

hcodes

H317,H334

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SLBD3664V
070M1532
107K1355

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H Narchi et al.
Journal of pediatric surgery, 23(9), 839-841 (1988-09-01)
Six children with shunt nephritis are reported of whom two did not show complete recovery of renal function. Follow up and outcome in relation to the delay in diagnosis and renal biopsy appearances are discussed.
Guanhao Bu et al.
Journal of the science of food and agriculture, 97(7), 2256-2262 (2016-10-19)
Soybean glycinin is considered a major allergenic protein, and glycation is widely used to reduce the allergenic potential of present allergens. Glycation of soybean glycinin with xylose at 55 °C for different lengths of time was investigated. The extent of Maillard
Dario Balestra et al.
International journal of molecular sciences, 20(17) (2019-08-28)
Mutations in the CDKL5 gene lead to an incurable rare neurological condition characterized by the onset of seizures in the first weeks of life and severe intellectual disability. Replacement gene or protein therapies could represent intriguing options, however, their application

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