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GBE1 抗体 (AA 527-556)

This anti-GBE1 antibody is a 兔 多克隆 antibody detecting GBE1 in WB 和 IF. Suitable for 人 和 小鼠.
产品编号 ABIN653459
发货至: 中国

Quick Overview for GBE1 抗体 (AA 527-556) (ABIN653459)

抗原

See all GBE1 抗体
GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

适用

  • 50
  • 11
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
人, 小鼠

宿主

  • 41
  • 9

克隆类型

  • 44
  • 6
多克隆

标记

  • 22
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GBE1 antibody is un-conjugated

应用范围

  • 41
  • 18
  • 13
  • 13
  • 11
  • 7
  • 6
  • 5
  • 4
  • 4
  • 3
  • 1
Western Blotting (WB), Immunofluorescence (IF)

克隆位点

RB24029
  • 抗原表位

    • 15
    • 6
    • 6
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 527-556

    纯化方法

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    免疫原

    This GBE1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 527-556 amino acids from the Central region of human GBE1.

    亚型

    Ig Fraction
  • 应用备注

    IF: 1:10~50. WB: 1:1000. WB: 1:1000

    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

    GBE1 (Glucan (1,4-alpha-), Branching Enzyme 1 (GBE1))

    别名

    GBE1

    背景

    GBE1 is a glycogen branching enzyme that catalyzes the transfer of alpha-1,4-linked glucosyl units from the outer end of a glycogen chain to an alpha-1,6 position on the same or a neighboring glycogen chain. Branching of the chains is essential to increase the solubility of the glycogen molecule and, consequently, in reducing the osmotic pressure within cells. Highest level of this enzyme are found in liver and muscle. Mutations in this gene are associated with glycogen storage disease IV (also known as Andersen's disease).

    分子量

    80474

    基因ID

    2632

    NCBI登录号

    NP_000149

    UniProt

    Q04446

    途径

    Cellular Glucan Metabolic Process
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