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ACAT1 抗体

ACAT1 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN631042
发货至: 中国
  • 抗原 See all ACAT1 抗体
    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
    适用
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    人, 小鼠, 大鼠
    宿主
    • 57
    • 8
    • 4
    克隆类型
    • 59
    • 10
    多克隆
    标记
    • 42
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    This ACAT1 antibody is un-conjugated
    应用范围
    • 41
    • 29
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    • 11
    • 6
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    • 3
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    Western Blotting (WB)
    纯化方法
    Affinity purified
    免疫原
    ACAT1 antibody was raised using a synthetic peptide corresponding to a region with amino acids SYTRSKAAWEAGKFGNEVIPVTVTVKGQPDVVVKEDEEYKRVDFSKVPKL
    Top Product
    Discover our top product ACAT1 Primary Antibody
  • 应用备注
    WB: 1 µg/mL
    Optimal conditions should be determined by the investigator.
    说明

    ACAT1 Blocking Peptide, catalog no. 33R-8958, is also available for use as a blocking control in assays to test for specificity of this ACAT1 antibody

    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ACAT1 antibody in PBS
    浓度
    Lot specific
    缓冲液
    PBS
    注意事项
    Avoid repeated freeze/thaw cycles.
    储存条件
    4 °C/-20 °C
    储存方法
    Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
  • 抗原
    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
    别名
    ACAT1 (ACAT1 产品)
    别名
    ACAT antibody, MAT antibody, T2 antibody, THIL antibody, RATACAL antibody, 6330585C21Rik antibody, Acat antibody, fd16h07 antibody, fd20g06 antibody, wu:fd16h07 antibody, wu:fd20g06 antibody, zgc:86832 antibody, acat1-a antibody, acetyl-CoA acetyltransferase 1 antibody, acetyl-Coenzyme A acetyltransferase 1 antibody, acetyl-CoA acetyltransferase 1 L homeolog antibody, ACAT1 antibody, Acat1 antibody, acat1 antibody, acat1.L antibody
    背景
    ACAT1 is a mitochondrially localized enzyme that catalyzes the reversible formation of acetoacetyl-CoA from two molecules of acetyl-CoA. The gene encoding ACAT1 spans approximately 27 kb and contains 12 exons interrupted by 11 introns. Defects in this gene are associated with the alpha-methylacetoaceticaciduria disorder, 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
    41 kDa (MW of target protein)
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