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CPT2 抗体 (N-Term)
CPT2
适用: 人
WB
宿主: 兔
Polyclonal
RB4657-4658
unconjugated
CPT2抗体详情
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抗原
See all CPT2 抗体
CPT2
(Carnitine Palmitoyltransferase 2 (CPT2))
抗原表位
All epitopes for CPT2 抗体
AA 6-38, N-Term
适用
All reactivities for CPT2 抗体
人
宿主
All hosts for CPT2 抗体
兔
克隆类型
All clonalities for CPT2 抗体
多克隆
标记
All conjugates for CPT2 抗体
This CPT2 antibody is un-conjugated
应用范围
All applications for CPT2 抗体
Western Blotting (WB)
预测反应
Pr
纯化方法
This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
免疫原
This CPT2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 6-38 amino acids from the N-terminal region of human CPT2.
克隆位点
RB4657-4658
亚型
Ig Fraction
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anti-Carnitine Palmitoyltransferase 2 (CPT2) (N-Term) antibody
CPT2
适用: 人, 小鼠, 大鼠, Cow, Pig, 马, 犬, 豚鼠, 兔, 斑马鱼
WB, IHC
宿主: 兔
Polyclonal
unconjugated
使用细节
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应用备注
WB: 1:1000. WB: 1:1000
限制
仅限研究用
贮存及处理
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状态
Liquid
缓冲液
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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
4 °C,-20 °C
储存方法
Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
有效期
6 months
CPT2目标详情
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抗原
CPT2
(Carnitine Palmitoyltransferase 2 (CPT2))
别名
CPT2 (CPT2 产品 )
别名
CPT1 antibody, CPTASE antibody, IIAE4 antibody, AI323697 antibody, CPTII antibody, cg2107 antibody, wu:fa03e08 antibody, wu:fb54a02 antibody, zgc:101627 antibody, carnitine palmitoyltransferase 2 antibody, carnitine O-palmitoyltransferase 2, mitochondrial antibody, carnitine palmitoyltransferase 2 S homeolog antibody, CPT2 antibody, LOC100214547 antibody, Cpt2 antibody, cpt2.S antibody, cpt2 antibody
背景
Carnitine palmitoyltransferase II precursor (CPT2) is a nuclear protein which is transported to the mitochondrial inner membrane. CPT2 together with carnitine palmitoyltransferase I oxidizes long-chain fatty acids in the mitochondria. Defects in this gene are associated with mitochondrial long-chain fatty-acid (LCFA) oxidation disorders.
分子量
73777
基因ID
1376
NCBI登录号
NP_000089
UniProt
P23786
途径
Regulation of Lipid Metabolism by PPARalpha , Monocarboxylic Acid Catabolic Process
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