产品名称
抗胆固醇-24羟化酶抗体,克隆1A7, clone 1A7, from mouse
biological source
mouse
conjugate
unconjugated
antibody form
purified immunoglobulin
antibody product type
primary antibodies
clone
1A7, monoclonal
species reactivity
mouse
species reactivity (predicted by homology)
rat (based on 100% sequence homology), human (based on 100% sequence homology), rabbit (based on 100% sequence homology)
technique(s)
immunocytochemistry: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable
isotype
IgG1κ
NCBI accession no.
UniProt accession no.
shipped in
wet ice
target post-translational modification
unmodified
Quality Level
Gene Information
human ... CYP46A1(10858)
Analysis Note
对照
小鼠脑裂解物
小鼠脑裂解物
通过蛋白质印迹在胆固醇24-羟化酶小鼠脑裂解物中进行了评估。
蛋白质印迹分析:1 µg/ml 的该抗体在 10 µg 胆固醇24-羟化酶小鼠脑裂解物中检测到胆固醇24-羟化酶。
蛋白质印迹分析:1 µg/ml 的该抗体在 10 µg 胆固醇24-羟化酶小鼠脑裂解物中检测到胆固醇24-羟化酶。
Application
使用经验证可用于WB、IP、IC、IH的抗胆固醇-24羟化酶抗体(克隆1A7)检测胆固醇-24羟化酶。
研究子类别
信号传导神经科学
信号传导神经科学
研究类别
神经科学
神经科学
Biochem/physiol Actions
该抗体识别胆固醇-24羟化酶。
Disclaimer
除非我们的产品目录或产品附带的其他公司文档另有说明,否则我们的产品仅供研究使用,不得用于任何其他目的,包括但不限于未经授权的商业用途、体外诊断用途、离体或体内治疗用途或任何类型的消费或应用于人类或动物。
General description
~54 kDa
在酶学中,胆固醇24-羟化酶(EC 1.14.13.98)是催化化学反应的酶:
胆固醇+NADPH+H++O2-->(24S)-24-羟基胆固醇+NADP++H2O。 胆固醇24-羟化酶,一种细胞色素P450(CYP46A1),在大脑中的表达水平比在肝脏中高100倍。该酶属于氧化还原酶家族,特别是作用于成对供体的那些,其中O2作为氧化剂并掺入或还原氧。 研究表明,胆固醇24-羟化酶是脑中胆固醇转换的主要组织特异性途径(Lund,2003)。
胆固醇+NADPH+H++O2-->(24S)-24-羟基胆固醇+NADP++H2O。 胆固醇24-羟化酶,一种细胞色素P450(CYP46A1),在大脑中的表达水平比在肝脏中高100倍。该酶属于氧化还原酶家族,特别是作用于成对供体的那些,其中O2作为氧化剂并掺入或还原氧。 研究表明,胆固醇24-羟化酶是脑中胆固醇转换的主要组织特异性途径(Lund,2003)。
Immunogen
His 标记的重组蛋白对应于人胆固醇24-羟化酶。
表位:未知
Other Notes
浓度:请参考批次特异性浓缩物的分析证书。
Physical form
在含 0.1 M Tris-甘氨酸(pH 7.4,150 mM NaCl )和 0.05% 叠氮化钠的缓冲液中的纯化的小鼠单克隆 IgG1κ。
形式:纯化
纯化的蛋白G
Preparation Note
自收到之日起,在 2-8°C 条件下可稳定保存1年
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存储类别
12 - Non Combustible Liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Fuxin Lu et al.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 41(2), 312-323 (2020-03-15)
The major pathway of brain cholesterol turnover relies on its hydroxylation into 24S-hydroxycholesterol (24S-HC) using brain-specific cytochrome P450 46A1 (CYP46A1). 24S-HC produced exclusively in the brain normally traverses the blood-brain barrier to enter the circulation to the liver for excretion;
Ahmed Haider et al.
Science translational medicine, 14(665), eadc9967-eadc9967 (2022-10-06)
Alterations in brain cholesterol homeostasis have been broadly implicated in neurological disorders. Notwithstanding the complexity by which cholesterol biology is governed in the mammalian brain, excess neuronal cholesterol is primarily eliminated by metabolic clearance via cytochrome P450 46A1 (CYP46A1). No
H Benson Peng et al.
Biopharmaceutics & drug disposition, 42(8), 372-388 (2021-07-06)
Age, hypercholesterolemia, and vitamin D deficiency are risk factors that increase the brain accumulation of pathogenic β-amyloid peptides (40 and 42), precursors leading to Alzheimer's disease (AD) in humans. The relative changes accompanying aging, high cholesterol, and/or treatment of calcitriol
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