GCNT1 anticorps (AA 88-117)

N° du produit ABIN389033

Détail du produit anti-GCNT1 anticorps

Antigène: GCNT1 (Glucosaminyl (N-Acetyl) Transferase 1, Core 2 (GCNT1))

Épitope: AA 88-117

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp GCNT1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Purification: This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

Immunogène: This GCNT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 88-117 amino acids from the Central region of human GCNT1.

Clone: RB4836

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. IHC-P: 1:50~100

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur GCNT1

Antigène: GCNT1 (Glucosaminyl (N-Acetyl) Transferase 1, Core 2 (GCNT1))

Autre désignation: GCNT1 (GCNT1 Produits)

Synonymes: anticorps C2GNT, anticorps C2GNT-L, anticorps C2GNT1, anticorps G6NT, anticorps NACGT2, anticorps NAGCT2, anticorps 5630400D21Rik, anticorps B130048E03, anticorps C2 GlcNAcT, anticorps IGnT, anticorps core 2 GlcNAc-T, anticorps glucosaminyl (N-acetyl) transferase 1, core 2 L homeolog, anticorps glucosaminyl (N-acetyl) transferase 1, core 2, anticorps gcnt1.L, anticorps GCNT1, anticorps Gcnt1

Sujet: Glycosylation is one of the most universal but at the same time complex protein modifications. Modification with sugar moeties can be both co- translational and post- translational, occurring in the endoplasmatic reticulum and golgi. Three different forms of glycosylation can be distinguished: N-linked oligosaccharides, O-linked oligosaccharides and glycosyl- phosphatidylinositol (GPI-) anchors. Glycosylation results in thousands of distinct, bioactive glycoproteins resident throughout the cell that strongly determine protein-protein, carbohydrate-protein, membrane, and adhesion properties. Diseases associated with glycosylation defects include Congenital disorders of glycosylation, (CDG), also known as carbohydrate deficient glycoprotein syndromes, and diseases associated with advanced aging.

Poids moléculaire: 49799

ID gène: 2650

NCBI Accession: NP_001091102, NP_001091103, NP_001091104, NP_001091105, NP_001481

UniProt: Q02742