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GBA 抗体 (C-Term)

This anti-GBA antibody is a 兔 多克隆 antibody detecting GBA in WB, ICC, IHC (p) 和 IF. Suitable for 人.
产品编号 ABIN2854995
发货至: 中国

Quick Overview for GBA 抗体 (C-Term) (ABIN2854995)

抗原

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

适用

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宿主

  • 92
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克隆类型

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多克隆

标记

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This GBA antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF)
  • 抗原表位

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    C-Term

    交叉反应

    Chimpanzee

    交叉反应 (详细)

    Chimpanzee (100 %)

    产品特性

    Rabbit Polyclonal antibody to GBA (glucosidase, beta, acid)
    GBA antibody [C1C3]

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Recombinant protein encompassing a sequence within the C-terminus region of human GBA. The exact sequence is proprietary.

    亚型

    IgG
  • 应用备注

    Suggested dilution Reference ICC/IF 1:100-1:1000* IHC (Formalin-fixed paraffin-embedded sections) 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceICC/IF1:100-1:1000* IHC (Formalin-fixed paraffin-embedded sections)1:100-1:1000* Western blot1:500-1:3000*

    说明

    Positive Control: 293T , A431 , H1299 , HeLaS3 , HepG2 , Molt-4 , Raji

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    0.82 mg/mL

    缓冲液

    0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.

    储存液

    Thimerosal (Merthiolate)

    注意事项

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple 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 encoding the same protein.

    Cellular Localization: Lysosome membrane, Peripheral membrane protein, Lumenal side

    分子量

    60 kDa

    基因ID

    2629

    途径

    Cellular Glucan Metabolic Process
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