ST3GAL5 anticorps (AA 80-200)
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- Antigène Voir toutes ST3GAL5 Anticorps
- ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))
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Épitope
- AA 80-200
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp ST3GAL5 est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- LYILKLNYTT EECDMKKMHY VDPDHVKRAQ KYAQQVLQKE CRPKFAKTSM ALLFEHRYSV DLLPFVQKAP KDSEAESKYD PPFGFRKFSS KVQTLLELLP EHDLPEHLKA KTCRRCVVIG S
- Réactivité croisée
- Humain, Souris, Rat
- Attributs du produit
- Polyclonal Antibodies
- Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 80-200 of human ST3GAL5 (NP_003887.3).
- Isotype
- IgG
- Top Product
- Discover our top product ST3GAL5 Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000
- Commentaires
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HIGH QUALITY
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- ST3GAL5 (ST3 beta-Galactoside alpha-2,3-Sialyltransferase 5 (ST3GAL5))
- Autre désignation
- ST3GAL5 (ST3GAL5 Produits)
- Synonymes
- anticorps SATI, anticorps SIAT9, anticorps SIATGM3S, anticorps ST3GalV, anticorps ST3GAL-V, anticorps 3S-T, anticorps Siat9, anticorps [a]2, anticorps ST3 beta-galactoside alpha-2,3-sialyltransferase 5, anticorps ST3GAL5, anticorps St3gal5
- Sujet
- Ganglioside GM3 is known to participate in the induction of cell differentiation, modulation of cell proliferation, maintenance of fibroblast morphology, signal transduction, and integrin-mediated cell adhesion. The protein encoded by this gene is a type II membrane protein which catalyzes the formation of GM3 using lactosylceramide as the substrate. The encoded protein is a member of glycosyltransferase family 29 and may be localized to the Golgi apparatus. Mutation in this gene has been associated with Amish infantile epilepsy syndrome. Transcript variants encoding different isoforms have been found for this gene.,ST3GAL5,SATI,SIAT9,SIATGM3S,SPDRS,ST3GalV,Signal Transduction,ST3GAL5
- Poids moléculaire
- 45 kDa/47 kDa
- ID gène
- 8869
- UniProt
- Q9UNP4
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