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ACAT1 抗体 (AA 201-300) (Cy7)

ACAT1 适用: 人 IF (cc), IF (p) 宿主: 兔 Polyclonal Cy7
产品编号 ABIN708467
发货至: 中国
  • 抗原 See all ACAT1 抗体
    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
    抗原表位
    • 14
    • 6
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 201-300
    适用
    • 67
    • 31
    • 26
    • 4
    • 4
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    宿主
    • 56
    • 8
    • 4
    克隆类型
    • 58
    • 10
    多克隆
    标记
    • 42
    • 5
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    This ACAT1 antibody is conjugated to Cy7
    应用范围
    • 41
    • 29
    • 22
    • 12
    • 12
    • 12
    • 11
    • 6
    • 6
    • 3
    • 2
    • 1
    Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    预测反应
    Human,Mouse,Rat,Dog,Rabbit
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human ACAT1
    亚型
    IgG
    Top Product
    Discover our top product ACAT1 Primary Antibody
  • 应用备注
    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    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
    -20 °C
    储存方法
    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
    有效期
    12 months
  • 抗原
    ACAT1 (Acetyl-CoA Acetyltransferase 1 (ACAT1))
    别名
    ACAT1 (ACAT1 产品)
    背景

    Synonyms: ACAT 1, ACAT, Acetoacetyl CoA thiolase, Acetyl CoA acetyltransferase, mitochondrial, Acetyl Coenzyme A acetyltransferase 1, MAT, RATACAL, T2, THIL, THIL_HUMAN, Acetyl-CoA acetyltransferase, mitochondrial, Acetoacetyl-CoA thiolase, T2.

    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. [provided by RefSeq, Feb 2009].

    基因ID
    38
    UniProt
    P24752
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