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ACAT1 抗体

ACAT1 适用: 人, 小鼠, 大鼠 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN7256768
发货至: 中国
  • 抗原 See all ACAT1 抗体
    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
    适用
    • 67
    • 30
    • 25
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    人, 小鼠, 大鼠
    宿主
    • 56
    • 8
    • 4
    克隆类型
    • 58
    • 10
    多克隆
    标记
    • 41
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    This ACAT1 antibody is un-conjugated
    应用范围
    • 40
    • 29
    • 21
    • 13
    • 13
    • 12
    • 10
    • 6
    • 6
    • 3
    • 2
    • 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 ACAT1 (NP_000010.1).
    亚型
    IgG
  • 应用备注
    WB 1:500-1:2000 IHC 1:50-1:200 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
    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
    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

    Observed_MW: 42 kDa

    Calculated_MW: 17 kDa/45 kDa

    基因ID
    38
    UniProt
    P24752
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