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GARS 抗体 (AA 43-289)

This anti-GARS antibody is a 小鼠 单克隆 antibody detecting GARS in WB 和 EIA. Suitable for 人.
产品编号 ABIN5540351
发货至: 中国

Quick Overview for GARS 抗体 (AA 43-289) (ABIN5540351)

抗原

See all GARS 抗体
GARS (Glycyl-tRNA Synthetase (GARS))

适用

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  • 2
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宿主

  • 43
  • 12
小鼠

克隆类型

  • 36
  • 19
单克隆

标记

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  • 2
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  • 1
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This GARS antibody is un-conjugated

应用范围

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  • 3
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Western Blotting (WB), Enzyme Immunoassay (EIA)

克隆位点

AT4E10
  • 抗原表位

    • 7
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    • 1
    • 1
    • 1
    • 1
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    AA 43-289

    纯化方法

    Protein-A affinity chromatography

    免疫原

    Recombinant human GARS (43-289aa) purified from E. coli.

    亚型

    IgG1
  • 应用备注

    The antibody has been tested by ELISA, Western blot analysis to assure specificity and reactivity. Since application varies, however, each investigation should be titrated by the reagent to obtain optimal results. Recommended starting dilution is 1:500

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS, pH 7.4 containing 0.02 % Sodium Azide and 10 % Glycerol

    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

    Store undiluted at 2-8°C for up to two weeks or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. Shelf life: one year from despatch.

    有效期

    12 months
  • 抗原

    GARS (Glycyl-tRNA Synthetase (GARS))

    别名

    glycyl-trna synthetase

    背景

    GARS, also known as glycyl-tRNA synthetase, is one of the aminoacyl-tRNA synthetase that charge tRNAs with their cognate amino acids. Defects in the gene encoding GlyRS is the cause of Charcot-Marie-Tooth disease type 2D (CMT2D), which is an autosomal dominant inherited disease characterized by severe weakness, atrophy and absence of deep tendon reflexes in the upper extremities. Defects in the GlyRS gene is also the cause of distal hereditary muscular neuropathy type V (HMN5), a disease similar to CMT2D, though the distal sensory involvement is less severe in HMN5 patients.

    UniProt

    P41250

    途径

    Ribonucleoside Biosynthetic Process
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