Name :
B3GAT3 Protein
Description :
B3GAT3, encoding beta-1,3-glucuronyltransferase 3, has an important role in proteoglycan biosynthesis. Homozygous B3GAT3 mutations have been associated with short stature, skeletal deformities, and congenital heart defects. There is a novel B3GAT3-related disorder with craniosynostosis and bone fragility, due to a unique homozygous mutation in B3GAT3.
Species :
Human
Uniprotkb :
E. coli
Tag :
His
Synonyms :
beta-1,3-glucuronyltransferase 3, glcUAT-I, GLCATI, β-1,3-glucuronyltransferase 3
Construction :
A DNA sequence encoding the human B3GAT3 (NP_036332.2) (Glu72-Val335) was expressed with a polyhistidine tag at the N-terminus.
Protein Purity :
> 85 % as determined by SDS-PAGE
Molecular Weight :
Approxiamtely 31.5 kDa
Endotoxin :
Please contact us for more information.
Formulatione :
Lyophilized from sterile PBS, pH 7.4. Please contact us for any concerns or special requirements. Normally 5 % – 8 % trehalose, mannitol and 0. 01% Tween 80 are added as protectants before lyophilization. Please refer to the specific buffer information in the hard copy of CoA.
Reconstitution :
A hardcopy of datasheet with reconstitution instructions is sent along with the products. Please refer to it for detailed information.
Stability & Storage :
Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Shipping :
In general, recombinant proteins are provided as lyophilized powder which are shipped at ambient temperature.Bulk packages of recombinant proteins are provided as frozen liquid. They are shipped out with blue ice unless customers require otherwise.
Research Background :
B3GAT3, encoding beta-1,3-glucuronyltransferase 3, has an important role in proteoglycan biosynthesis. Homozygous B3GAT3 mutations have been associated with short stature, skeletal deformities, and congenital heart defects. There is a novel B3GAT3-related disorder with craniosynostosis and bone fragility, due to a unique homozygous mutation in B3GAT3.
References and Literature :
Related category websites: https://www.medchemexpress.com/recombinant-proteins.html
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