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Beta-galactoside alpha-2,6-sialyltransferase 1

SIGMA/SAE0090 - ≥300 units/mg protein, ST6GAL1 human recombinant, expressed in HEK 293 cells

Synonym: Alpha 2,6-ST 1; B-cell antigen CD75; CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,6-sialyltransferase 1; ST6Gal I; Sialyltransferase 1

Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-SAE0090-10UG 10 µg
$401.00
1/EA
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The purity of Beta-galactoside alpha-2,6-sialyltransferase 1 human, recombinant (Cat. No. SAE0090) was assessed on SDS-PAGE stained with InstantBlue™ (Cat. No. ISB1L).
Activity Comparison of ST6GAL1 ST6GAL1 human recombinant ability to transfer sialic acid from CMP-NANA to asialofetuin was found to be significantly higher than the activity of ST6GAL1 from Photobacterium damsela. Purple: ST6GAL1 human recombinant, expressed in HEK 293 cells (Cat. No. SAE0090).Red: recombinant ST6GAL1 from Photobacterium damsela expressed in E. coli.
Transferring sialic acid from cytidine-monophosphate (CMP) onto Asialofetuin (Cat. No. A4781) has been studied using Beta-galactoside alpha-2,6-sialyltransferase 1 human, recombinant (ST6GAL1) (Cat. No. SAE0090) followed by LC/Q-TOF MS. Extracted ion chromatograms of common sialylated glycan fragments ions (MSE), m/z 292.1 (Neu5Ac + H)+ and m/z 657.2 (HexNAc + Hex + Neu5Ac + H)+ ,with and without ST6GAL1 are overlaid showing significantly higher levels of sialylated glycan fragments ions after enzyme activity.

 

assay ≥95% (SDS-PAGE)
description The specific activity of ST6Gal I is measured by its ability to transfer sialic acid from CMP-NANA to asialofetuin.
form lyophilized powder
recombinant expressed in HEK 293 cells
shipped in ambient
specific activity ≥300 units/mg protein
storage temp. −20°C
Biochem/physiol Actions: ST6Gal I catalyzes the transfer of CMP-N-acetylneuraminate (CMP-sialic acid, CMP-NANA) to the β-D-galactosyl-1,4-N-acetyl-D-glucosaminyl termini on glycoproteins. Sialic acids are distributed in a variety of glycolipids and glycoproteins.1 The sialic acid that is added to a galactose (Gal) can be bound either to the hydroxyl attached to carbon-3 of Gal to form an α-2,3 glycosidic linkage, or to the hydroxyl group attached to carbon-6 to form an α-2,6 glycosidic linkage.1 ST6Gal I generates a α-2,6 linkage of sialic acid on the non-reducing, terminal Galβ1 4GlcNAc residues of oligosaccharides and glycoconjugates.2

Terminal sialylation has been shown to decrease Fcγ receptor binding and increase anti-inflammatory activity,3 as well as antibody-dependent cellular cytotoxicity in different studies by reduced binding of sialylated antibody towards FcγRIIIa.4-5

This recombinant ST6Gal I product can be used to study the mode of action of the enzyme, as well as its potential inhibitors. It can also be used as a glycoengineering tool to modify glycoproteins in vitro.

CMP-N-acetylneuraminate (CMP-sialic acid, CMP-NANA) to the β-D-galactosyl-1,4-N-acetyl-D-glucosaminyl termini on glycoproteins.
Sialic acids are distributed in a variety of glycolipids and glycoproteins. The sialic acid that is added to a galactose (Gal) can be bound either to the hydroxyl attached to carbon-3 of Gal to form an α-2,3 glycosidic linkage, or to the hydroxyl group attached to carbon-6 to form an α-2,6 glycosidic linkage. ST6Gal I generates a α-2,6 linkage of sialic acid on the non-reducing, terminal Galβ1 4GlcNAc residues of oligosaccharides and glycoconjugates.

Terminal sialylation has been shown to decrease Fcγ receptor binding and increase anti-inflammatory activity, as well as antibody-dependent cellular cytotoxicity in different studies by reduced binding of sialylated antibody towards FcγRIIIa.
General description: Recombinant human Beta-galactoside alpha-2,6-sialyltransferase 1 (ST6Gal I) is expressed in human HEK 293 cells as a glycoprotein with a calculated molecular mass of 43.5 kDa (amino acids 27-406). The DTT-reduced protein migrates as a ~50 kDa polypeptide on SDS-PAGE due to glycosylation. This protein is manufactured in human cells, with no serum. The human cells expression system allows human-like glycosylation and folding, and often supports higher specific activity of the protein. The protein is produced with no artificial tags.
Other Notes: One unit is defined as the amount of enzyme required to transfer 1.0 nanomole of sialic acid from CMP-NANA to asialofetuin per minute at pH 6.0, 37oC.
RIDADR NONH for all modes of transport
WGK Germany WGK 2
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥95% (SDS-PAGE)
activity specific activity: ≥300 units/mg protein
Storage Temp. −20°C
Enzyme Commission (EC) Number 2.4.99.1   ( BRENDA  | IUBMB  )
UNSPSC 12352202

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