电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

GCNT1 抗体 (Center)

GCNT1 适用: 人, 小鼠 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6295417
发货至: 中国
  • 抗原 See all GCNT1 抗体
    GCNT1 (Glucosaminyl (N-Acetyl) Transferase 1, Core 2 (GCNT1))
    抗原表位
    • 7
    • 7
    • 7
    • 6
    • 6
    • 6
    • 4
    • 3
    • 1
    • 1
    AA 88-117, Center
    适用
    人, 小鼠
    宿主
    • 32
    • 2
    • 1
    克隆类型
    • 35
    多克隆
    标记
    • 15
    • 4
    • 4
    • 4
    • 4
    • 4
    This GCNT1 antibody is un-conjugated
    应用范围
    请咨询
    原理
    Rabbit Anti-GCNT1 (Center) Antibody
    免疫原
    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.
    Top Product
    Discover our top product GCNT1 Primary Antibody
  • 限制
    仅限研究用
  • 储存条件
    4 °C,-20 °C
    储存方法
    2-8°C (short-term), -20°C (long-term)
  • 抗原
    GCNT1 (Glucosaminyl (N-Acetyl) Transferase 1, Core 2 (GCNT1))
    别名
    GCNT1 (GCNT1 产品)
    别名
    C2GNT antibody, C2GNT-L antibody, C2GNT1 antibody, G6NT antibody, NACGT2 antibody, NAGCT2 antibody, 5630400D21Rik antibody, B130048E03 antibody, C2 GlcNAcT antibody, IGnT antibody, core 2 GlcNAc-T antibody, glucosaminyl (N-acetyl) transferase 1, core 2 L homeolog antibody, glucosaminyl (N-acetyl) transferase 1, core 2 antibody, gcnt1.L antibody, GCNT1 antibody, Gcnt1 antibody
    背景

    Target Description: 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.

    Gene Symbol: GCNT1

    基因ID
    2650
    UniProt
    Q02742
You are here:
客服