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Recombinant Human ST3GAL3, His-tagged

Cat.No. : ST3GAL3-232H
Product Overview : Human ST3GAL3 partial(aa 218 to 359) was expressed in E. coli.
  • Specification
  • Gene Information
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Description : The protein encoded by this gene is a type II membrane protein that catalyzes the transfer of sialic acid from CMP-sialic acid to galactose-containing substrates. The encoded protein is normally found in the Golgi apparatus but can be proteolytically processed to a soluble form. This protein is a member of glycosyltransferase family 29. Mutations in this gene have been associated with autosomal recessive nonsymdromic mental retardation-12 (MRT12). Multiple transcript variants encoding several different isoforms have been found for this gene.
Source : E. coli
Species : Human
Tag : His
Form : Lyophilised
Protein length : 218 to 359
AA Sequence : QDFKWLKYIVYKERVSASDGFWKSVATRVPKEPPEIRILN PYFIQEAAF TLIGLPFNNGLMGRGNIPTLGSVAVTMAL HGCDEVAVAGFGYDMSTPNA PLHYYETVRMAAIKESWT HNIQREKEFLRKLVKARVITDLSSGI
Applications : Mass Spectrometry; SDS-PAGE
Storage : Shipped at 4°C. Upon delivery aliquot and store at -80ºC. Avoid freeze / thaw cycles.
Concentration : Reconstitution Dependent
Preservative : None
Reconstitution : Reconstitute with 63 µl aqua dest.
Gene Name : ST3GAL3 ST3 beta-galactoside alpha-2,3-sialyltransferase 3 [ Homo sapiens (human) ]
Official Symbol : ST3GAL3
Synonyms : ST3GAL3; ST3N; MRT12; SIAT6; EIEE15; ST3GALII; ST3GalIII; ST3 beta-galactoside alpha-2,3-sialyltransferase 3; CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase; ST3Gal III; alpha 2,3-ST 3; alpha-2,3-sialyltransferase II; alpha 2,3-sialyltransferase III; Gal beta-1,3(4)GlcNAc alpha-2,3 sialyltransferase; sialyltransferase 6 (N-acetyllacosaminide alpha 2,3-sialyltransferase); NP_001257388.1; NP_001257389.1; NP_001257390.1; NP_001257391.1; NP_001257392.1; NP_001257393.1; NP_001257394.1; EC 2.4.99.6; NP_001257395.1; NP_006270.1; NP_777623.2; NP_777624.1; NP_777625.1; NP_777626.1; NP_777627.1; NP_777628.2; NP_777629.1; NP_777630.1; NP_777631.2
Gene ID : 6487
mRNA Refseq : NM_006279
Protein Refseq : NP_006270
MIM : 606494
UniProt ID : Q11203
Chromosome Location : 1p34.1
Pathway : Glycosaminoglycan biosynthesis - keratan sulfate; Glycosphingolipid biosynthesis - lacto and neolacto series; MPS I - Hurler syndrome
Function : N-acetyllactosaminide alpha-2,3-sialyltransferase activity; beta-galactoside (CMP) alpha-2,3-sialyltransferase activity

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