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GCNT1 抗体 (AA 88-117)

GCNT1 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB4836 unconjugated
产品编号 ABIN389033
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
    • 6
    • 6
    • 6
    • 6
    • 4
    • 3
    • 1
    • 1
    AA 88-117
    适用
    人, 小鼠
    宿主
    • 31
    • 2
    • 1
    克隆类型
    • 34
    多克隆
    标记
    • 14
    • 4
    • 4
    • 4
    • 4
    • 4
    This GCNT1 antibody is un-conjugated
    应用范围
    • 34
    • 27
    • 13
    • 3
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
    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.
    克隆位点
    RB4836
    亚型
    Ig Fraction
    Top Product
    Discover our top product GCNT1 Primary Antibody
  • 应用备注
    WB: 1:1000. IHC-P: 1:50~100
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    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.
    有效期
    6 months
  • 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
    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.
    分子量
    49799
    基因ID
    2650
    NCBI登录号
    NP_001091102, NP_001091103, NP_001091104, NP_001091105, NP_001481
    UniProt
    Q02742
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