CPT2 抗体
Quick Overview for CPT2 抗体 (ABIN7000926)
抗原
See all CPT2 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Synthetic peptide of human CPT2
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亚型
- IgG
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anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 1-180) antibody
CPT2 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (Internal Region) antibodyCPT2 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 141-154) antibodyVerified CPT2 适用: 人, 小鼠, 大鼠 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 1-658) antibodyCPT2 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 388-551) antibodyCPT2 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 212-241) antibodyCPT2 适用: 人 WB 宿主: 兔 Polyclonal RB41839 unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 351-450) antibodyCPT2 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 1-658) antibodyCPT2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 351-450) antibodyCPT2 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1G7 unconjugated
anti-Carnitine Palmitoyltransferase 2 (CPT2) (AA 401-500) antibodyCPT2 适用: 小鼠 WB, ELISA, IF (cc), IHC (p), IF (p), IHC (fro) 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB 1:500-1:2000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.7 mg/mL
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缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- CPT2 (Carnitine Palmitoyltransferase 2 (CPT2))
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别名
- CPT2
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背景
- The protein encoded by this gene is a nuclear protein which is transported to the mitochondrial inner membrane. Together with carnitine palmitoyltransferase I, the encoded protein oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders.
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分子量
- 74 kDa
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NCBI登录号
- NP_000089
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UniProt
- P23786
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途径
- Regulation of Lipid Metabolism by PPARalpha, Monocarboxylic Acid Catabolic Process
抗原
-
