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ACAT1 抗体 (AA 34-187)

This anti-ACAT1 antibody is a 兔 多克隆 antibody detecting ACAT1 in WB, IHC, ELISA, IF 和 IP. Suitable for 人, 小鼠 和 大鼠.
产品编号 ABIN5702031
发货至: 中国

Quick Overview for ACAT1 抗体 (AA 34-187) (ABIN5702031)

抗原

See all ACAT1 抗体
ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

适用

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  • 34
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  • 1
人, 小鼠, 大鼠

宿主

  • 60
  • 5
  • 4

克隆类型

  • 59
  • 10
多克隆

标记

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  • 5
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
  • 1
  • 1
This ACAT1 antibody is un-conjugated

应用范围

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  • 27
  • 25
  • 13
  • 13
  • 10
  • 8
  • 8
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  • 3
  • 3
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF), Immunoprecipitation (IP)
  • 抗原表位

    • 15
    • 6
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 34-187

    原理

    ACAT1 antibody

    免疫原

    Immunogen sequence: 34-187aa

    Immunogen: acetyl-Coenzyme A acetyltransferase 1

    亚型

    IgG
  • 应用备注

    WB :1:500-1:5000,IF:1:10-1:100,IHC:1:20-1:200,IP:1:200-1:2000,

    说明

    human skeletal muscle tissue were subjected to SDS PAGE followed by western blot with FNab00072(ACAT1 antibody) at dilution of 1:500

    限制

    仅限研究用
  • 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

    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))

    别名

    ACAT1

    背景

    Synonyms: Acetyl-CoA acetyltransferase, mitochondrial|Acetoacetyl-CoA thiolase|T2|ACAT1|ACAT|MAT

    Background: This gene encodes a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. Defects in this gene are associated with 3-ketothiolase deficiency, an inborn error of isoleucine catabolism characterized by urinary excretion of 2-methyl-3-hydroxybutyric acid, 2-methylacetoacetic acid, tiglylglycine, and butanone.

    分子量

    17kDa,observed 45kDa

    基因ID

    38

    UniProt

    P24752
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