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SGSH 抗体 (C-Term)

SGSH 适用: 人 WB 宿主: 兔 Polyclonal RB24406 unconjugated
产品编号 ABIN653531
发货至: 中国
  • 抗原 See all SGSH 抗体
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    抗原表位
    • 15
    • 12
    • 9
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 420-449, C-Term
    适用
    • 31
    • 19
    • 6
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 43
    • 3
    • 1
    克隆类型
    • 46
    • 1
    多克隆
    标记
    • 22
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This SGSH antibody is un-conjugated
    应用范围
    • 45
    • 17
    • 13
    • 13
    • 7
    • 4
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This SGSH antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 420-449 amino acids from the C-terminal region of human SGSH.
    克隆位点
    RB24406
    亚型
    Ig Fraction
    Top Product
    Discover our top product SGSH Primary Antibody
  • 应用备注
    WB: 1:4000
    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
    SGSH (N-Sulfoglucosamine Sulfohydrolase (SGSH))
    别名
    SGSH (SGSH 产品)
    别名
    HSS antibody, MPS3A antibody, SFMD antibody, 4632406A19Rik antibody, N-sulfoglucosamine sulfohydrolase antibody, N-sulfoglucosamine sulfohydrolase (sulfamidase) antibody, SGSH antibody, Sgsh antibody
    背景
    SGSH is one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined.
    分子量
    56695
    基因ID
    6448
    NCBI登录号
    NP_000190
    UniProt
    P51688
    途径
    Glycosaminoglycan Metabolic Process
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