电话:
+86 (0512) 65829739
传真:
+86 (010) 6788 5057
电子邮件:
orders@antibodies-online.cn

GBA 抗体

This anti-GBA antibody is a 兔 多克隆 antibody detecting GBA in WB, IHC 和 ELISA. Suitable for 人 和 小鼠.
产品编号 ABIN7248746
发货至: 中国

Quick Overview for GBA 抗体 (ABIN7248746)

抗原

See all GBA 抗体
GBA (Glucosidase, Beta, Acid (GBA))

适用

  • 75
  • 45
  • 34
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
人, 小鼠

宿主

  • 92
  • 12

克隆类型

  • 84
  • 20
多克隆

标记

  • 45
  • 20
  • 12
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GBA antibody is un-conjugated

应用范围

  • 73
  • 40
  • 25
  • 24
  • 13
  • 11
  • 11
  • 9
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Antigen affinity purification

    免疫原

    Synthetic peptide of human GBA

    亚型

    IgG
  • 应用备注

    WB 1:500-1:2000, IHC 1:50-1:100, ELISA 1:5000-1:10000

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.56 mg/mL

    缓冲液

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    -20 °C

    储存方法

    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原

    GBA (Glucosidase, Beta, Acid (GBA))

    别名

    GBA

    背景

    This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.

    分子量

    Observed_MW: Refer to figures

    Calculated_MW: 60 kDa

    UniProt

    P04062

    途径

    Cellular Glucan Metabolic Process
You are here:
Chat with us!