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SUCLG1 抗体

This 兔 多克隆 antibody specifically detects SUCLG1 in WB, IF, IP, ICC 和 IHC (p). It exhibits reactivity toward 人.
产品编号 ABIN2856658
发货至: 中国
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Tel +86 (0512) 65829739 传真 +86 (010) 6788 5057

Quick Overview for SUCLG1 抗体 (ABIN2856658)

抗原

See all SUCLG1 抗体
SUCLG1 (Succinate-CoA Ligase, alpha Subunit (SUCLG1))

适用

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宿主

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克隆类型

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多克隆

标记

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This SUCLG1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunofluorescence (IF), Immunoprecipitation (IP), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

质量等级

KO Validated
  • 特异性

    Knockdown/Knockout validation was supported by references (PMID:26990993)

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Rabbit Polyclonal antibody to SUCLG1 (succinate-CoA ligase, alpha subunit)
    SUCLG1 antibody

    纯化方法

    Purified by antigen-affinity chromatography.

    免疫原

    Full length human SUCLG1 Recombinant protein.

    亚型

    IgG
  • 应用备注

    WB: 1:1000-1:10000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    说明

    Positive Control: Rat brain , Mouse brain

    Validation: KO/KD

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1.48 mg/mL

    缓冲液

    1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300

    储存液

    ProClin

    注意事项

    This product contains ProClin: 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 as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • 抗原

    SUCLG1 (Succinate-CoA Ligase, alpha Subunit (SUCLG1))

    别名

    succinate-CoA ligase alpha subunit

    背景

    This gene encodes the alpha subunit of the heterodimeric enzyme succinate coenzyme A ligase. This enzyme is targeted to the mitochondria and catalyzes the conversion of succinyl CoA and ADP or GDP to succinate and ATP or GTP. Mutations in this gene are the cause of the metabolic disorder fatal infantile lactic acidosis and mitochondrial DNA depletion.

    Cellular Localization: Mitochondrion

    分子量

    36 kDa

    基因ID

    8802

    UniProt

    P53597
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