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GLA 抗体 (AA 80-429)

This 小鼠 单克隆 anti-GLA antibody (Clone 7F1) specifically detects GLA in WB, IHC, ELISA 和 IF. The antibody is reactive with 人 samples.
产品编号 ABIN7114449
发货至: 中国
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中国
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
4A Biotech Co.,Ltd.
Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for GLA 抗体 (AA 80-429) (ABIN7114449)

抗原

See all GLA 抗体
GLA (Galactosidase, alpha (GLA))

适用

  • 98
  • 37
  • 27
  • 4
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  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
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宿主

  • 106
  • 12
  • 2
小鼠

克隆类型

  • 88
  • 32
单克隆

标记

  • 55
  • 14
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  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
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  • 1
  • 1
  • 1
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This GLA antibody is un-conjugated

应用范围

  • 85
  • 36
  • 33
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  • 23
  • 17
  • 13
  • 13
  • 12
  • 6
  • 4
  • 3
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Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

克隆位点

7F1
  • 抗原表位

    • 16
    • 9
    • 7
    • 6
    • 5
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
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    AA 80-429

    原理

    GLA antibody

    纯化方法

    Protein A+G purification

    纯度

    ≥95 % as determined by SDS-PAGE

    免疫原

    Immunogen sequence: 80-429aa

    Immunogen: galactosidase, alpha

    亚型

    IgG2a
  • 应用备注

    WB: 1:500-1:2000, IHC: 1:20-1:200, IF: 1:20-1:200

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    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.

    注意事项

    Avoid repeated freeze / thaw cycles.

    储存条件

    -20 °C

    储存方法

    -20°C for 12 months

    有效期

    12 months
  • 抗原

    GLA (Galactosidase, alpha (GLA))

    别名

    GLA

    背景

    Synonyms: Alpha-galactosidase A|Alpha-D-galactosidase A|Alpha-D-galactoside galactohydrolase|Galactosylgalactosylglucosylceramidase GLA|Melibiase|GLA

    Background: GLA, also named as Melibiase, Agalsidase and Alpha-galactosidase A, belongs to the glycosyl hydrolase 27 family. It hydrolyzes terminal, non-reducing alpha-D-galactose residues in alpha-D-galactosides, including galactose oligosaccharides, galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy(ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease, a lysosomal storage disease.

    分子量

    49 kDa

    基因ID

    2717

    UniProt

    P06280

    途径

    SARS-CoV-2 Protein Interactome
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