推荐产品
生物源
mouse
品質等級
抗體表格
purified antibody
抗體產品種類
primary antibodies
無性繁殖
AE-1, monoclonal
物種活性
canine, bovine, human, chicken, guinea pig, monkey
製造商／商標名
Chemicon®
技術
ELISA: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
同型
IgG1
NCBI登錄號
UniProt登錄號
運輸包裝
wet ice
目標翻譯後修改
unmodified
基因資訊
human ... ACHE(43)
特異性
Acetylcholinesterase from human and monkey.
免疫原
Acetylcholinesterase AChE from human erythrocyte.
應用
ELISA
Immunohistochemistry
Western Blot
Optimal working dilutions must be determined by end user.
Immunohistochemistry
Western Blot
Optimal working dilutions must be determined by end user.
Research Category
Neuroscience
Neuroscience
Research Sub Category
Neurotransmitters & Receptors
Neuronal & Glial Markers
Neurotransmitters & Receptors
Neuronal & Glial Markers
This Anti-Acetylcholinesterase Antibody, clone AE-1 is validated for use in ELISA, IH, IP for the detection of Acetylcholinesterase.
外觀
Format: Purified
Liquid in 0.02M PB, 0.25M NaCl, pH 7.6, with 0.1% sodium azide.
儲存和穩定性
Maintain at 2-8°C for up to 6 months.
其他說明
Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.
法律資訊
CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
免責聲明
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
未找到合适的产品？
试试我们的产品选型工具.
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Pamela Jarrett et al.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 45(2), 150-157 (2018-03-07)
Neuronal ceroid-lipofuscinoses are a heterogeneous group of inherited disorders in which abnormal lipopigments form lysosomal inclusion bodies in neurons. Kufs disease is rare, and clinical symptoms include seizures, progressive cognitive impairment, and myoclonus. Most cases of Kufs disease are autosomal
Sin Yeang Teow et al.
BMC biotechnology, 13, 107-107 (2013-12-07)
HIV genome is packaged and organized in a conical capsid, which is made up of ~1,500 copies of the viral capsid protein p24 (CA). Being a primary structural component and due to its critical roles in both late and early
Franziska Richter et al.
EBioMedicine, 41, 649-658 (2019-03-02)
The most prevalent inherited form of generalized dystonia is caused by a mutation in torsinA (DYT1, ∆GAG) with incomplete penetrance. Rodent models with mutated torsinA do not develop dystonic symptoms, but previous ex vivo studies indicated abnormal excitation of cholinergic
Axodendritic contacts onto calcium/calmodulin-dependent protein kinase type II-expressing neurons in the barn owl auditory space map.
Rodriguez-Contreras, A; Liu, XB; DeBello, WM
The Journal of Neuroscience null
Alicia J Dafferner et al.
Chemical research in toxicology, 30(10), 1897-1910 (2017-09-12)
Nerve agents and organophosphorus pesticides make a covalent bond with the active site serine of acetylcholinesterase (AChE), resulting in inhibition of AChE activity and toxic symptoms. AChE in red blood cells (RBCs) serves as a surrogate for AChE in the
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门