C5868
β-Conglycinin from Glycine max (soybean)
soybean storage protein
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About This Item
UNSPSC Code:
12352202
Recommended Products
biological source
Glycine max (soybean)
Assay
≥80% (HPLC)
form
powder
UniProt accession no.
storage temp.
−20°C
Gene Information
soybean ... CG-1(548007)
General description
β-Conglycinin is widely reported to show favorable effects on lipid metabolism, reducing serum and liver cholesterol, lowering plasma VLDL, preventing cirrhosis, and inhibiting lipogenesis.
β-Conglycinin is a major storage protein in soy and is a soluble glycoprotein that exists in a heterotrimeric form. β-Conglycinin consists of α, α′, and β subunits
Application
β-Conglycinin is a major storage protein in soy and is a soluble glycoprotein that exists in a heterotrimeric form. It has been shown to enhance fullness and reduce hunger sensations in healthy adults and in rats by having cholecystokinin (CCK) secretion activity.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Soybean β-conglycinin bromelain hydrolysate stimulates cholecystokinin secretion by enteroendocrine STC-1 cells to suppress the appetite of rats under meal-feeding conditions.
Sufian KN., et al.
Biosciences, Biotechnology Research Asia, 75, 848-853 (2011)
Barbara Sciandrone et al.
Biochimica et biophysica acta. Gene regulatory mechanisms, 1862(8), 786-795 (2019-07-13)
The Lipid A moiety of the lipopolysaccharide can be covalently modified during its transport to the outer membrane by different enzymes, among which the LpxT inner membrane protein. LpxT transfers a phosphate group from the undecaprenyl pyrophosphate to the Lipid
Takashi Nishi et al.
The Journal of nutrition, 133(8), 2537-2542 (2003-07-31)
We previously demonstrated that soybean beta-conglycinin peptone suppresses food intake and gastric emptying by direct action on rat small intestinal mucosal cells to stimulate cholecystokinin (CCK) release. The aim of the present study was to define the active fragment in
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