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DLAT 抗体

This anti-DLAT antibody is a 兔 多克隆 antibody detecting DLAT in WB, IHC 和 IF. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN7257932
发货至: 中国

Quick Overview for DLAT 抗体 (ABIN7257932)

抗原

See all DLAT 抗体
DLAT (Dihydrolipoyl Transacetylase (DLAT))

适用

  • 63
  • 27
  • 21
  • 7
  • 6
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 62
  • 7

克隆类型

  • 60
  • 9
多克隆

标记

  • 42
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
This DLAT antibody is un-conjugated

应用范围

  • 51
  • 30
  • 23
  • 17
  • 15
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  • 4
  • 3
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • 产品特性

    Polyclonal Antibody

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein of human DLAT (NP_001922.2).

    亚型

    IgG
  • 应用备注

    WB 1:500-1:2000 IHC 1:50-1:100 IF 1:50-1:200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    PBS with 0.02 % sodium azide, 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.

    储存条件

    -20 °C

    储存方法

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

    DLAT (Dihydrolipoyl Transacetylase (DLAT))

    别名

    DLAT

    背景

    This gene encodes component E2 of the multi-enzyme pyruvate dehydrogenase complex (PDC). PDC resides in the inner mitochondrial membrane and catalyzes the conversion of pyruvate to acetyl coenzyme A. The protein product of this gene, dihydrolipoamide acetyltransferase, accepts acetyl groups formed by the oxidative decarboxylation of pyruvate and transfers them to coenzyme A. Dihydrolipoamide acetyltransferase is the antigen for antimitochondrial antibodies. These autoantibodies are present in nearly 95 % of patients with the autoimmune liver disease primary biliary cirrhosis (PBC). In PBC, activated T lymphocytes attack and destroy epithelial cells in the bile duct where this protein is abnormally distributed and overexpressed. PBC enventually leads to cirrhosis and liver failure. Mutations in this gene are also a cause of pyruvate dehydrogenase E2 deficiency which causes primary lactic acidosis in infancy and early childhood.

    分子量

    Observed_MW: 69 kDa

    Calculated_MW: 68 kDa

    基因ID

    1737

    UniProt

    P10515
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