Products
ST3GAL3 antibody
Category:
Research Area:
Synonyms: | CMP-N-acetylneuraminate-beta-1 antibody, 4-galactoside alpha-2 antibody, 3-sialyltransferase|Beta-galactoside alpha-2 antibody, 3-sialyltransferase 3 (Alpha 2 antibody, 3-ST 3)|Gal beta-1 antibody, 3(4) GlcNAc alpha-2 antibody, 3 sialyltransferase|N-acetyllactosaminide alpha-2 antibody, 3-sialyltransferase|ST3Gal III (ST3GalIII)|ST3N|Sialyltransferase 6|ST3GAL3|SIAT6 antibody | ||
Catalogue No.: | FNab08264 | Reactivity: | Human, Mouse, Rat |
Host: | Rabbit | Tested Application: | ELISA, WB, IHC, IF |
Clonality: | polyclonal | Isotype: | IgG |
- SPECIFICATIONS
- Product Name
- ST3GAL3 antibody
- Catalogue No.
- FNab08264
- Size
- 100μg
- Form
- liquid
- Purification
- Immunogen affinity purified
- Purity
- ≥95% as determined by SDS-PAGE
- Clonality
- polyclonal
- Isotype
- IgG
- Storage
- PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
Immunogen
- Immunogen
- ST3 beta-galactoside alpha-2, 3-sialyltransferase 3
- Alternative Names
- CMP-N-acetylneuraminate-beta-1 antibody, 4-galactoside alpha-2 antibody, 3-sialyltransferase|Beta-galactoside alpha-2 antibody, 3-sialyltransferase 3 (Alpha 2 antibody, 3-ST 3)|Gal beta-1 antibody, 3(4) GlcNAc alpha-2 antibody, 3 sialyltransferase|N-acetyllactosaminide alpha-2 antibody, 3-sialyltransferase|ST3Gal III (ST3GalIII)|ST3N|Sialyltransferase 6|ST3GAL3|SIAT6 antibody
- UniProt ID
- Q11203
- Observed MW
- 50 kDa
Application
- Tested Applications
- ELISA, WB, IHC, IF
- Recommended dilution
- WB: 1:500 - 1:2000; IHC: 1:50 - 1:200; IF: 1:50 - 1:200
Validated Images
Rat liver tissue were subjected to SDS PAGE followed by western blot with FNab08264(ST3GAL3 antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded human liver injury using FNab08264(ST3GAL3 antibody) at dilution of 1:100
- Background
- 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.